Variant report

Variant	rs3735530
Chromosome Location	chr7:27189982-27189983
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SMARCC1	chr7:27189782-27191078	Hela-S3	cervix:	n/a	n/a
2	SMC3	chr7:27189834-27190826	Hela-S3	cervix:	n/a	n/a
3	TBP	chr7:27189961-27190161	HepG2	liver:	n/a	n/a
4	REST	chr7:27189942-27191024	A549	lung:	n/a	chr7:27190942-27190955 chr7:27190847-27190856 chr7:27190353-27190362 chr7:27190348-27190368 chr7:27190349-27190367 chr7:27190354-27190368 chr7:27190348-27190368
5	CTCF	chr7:27189940-27190090	GM12878	blood:	n/a	n/a
6	TAF1	chr7:27189918-27190793	A549	lung:	n/a	n/a
7	POLR2A	chr7:27189947-27190970	A549	lung:	n/a	n/a
8	ZNF263	chr7:27189861-27191256	HEK293-T-REx	kidney:	n/a	n/a
9	YY1	chr7:27189958-27190759	HepG2	liver:	n/a	chr7:27190570-27190584 chr7:27190641-27190652 chr7:27190638-27190652
10	MAX	chr7:27189704-27190915	A549	lung:	n/a	chr7:27190352-27190361
11	MAX	chr7:27189901-27190791	Hela-S3	cervix:	n/a	chr7:27190352-27190361
12	POLR2A	chr7:27189859-27190567	HepG2	liver:	n/a	n/a
13	POLR2A	chr7:27189921-27191037	A549	lung:	n/a	n/a
14	CTCF	chr7:27189880-27190030	AoAF	blood vessel:	n/a	n/a
15	POLR2A	chr7:27189954-27191240	Raji	blood:	n/a	n/a
16	CTCF	chr7:27189960-27190110	AG09319	gingival:	n/a	n/a
17	CTCF	chr7:27189880-27190030	WERI-Rb-1	eye:	n/a	n/a
18	POLR2A	chr7:27189887-27191136	HCT-116	colon:	n/a	n/a
19	SMARCB1	chr7:27189768-27191238	Hela-S3	cervix:	n/a	n/a
20	REST	chr7:27189894-27190757	PANC-1	pancreas:	n/a	chr7:27190353-27190362 chr7:27190348-27190368 chr7:27190349-27190367 chr7:27190354-27190368 chr7:27190348-27190368
21	REST	chr7:27189975-27191043	GM12878	blood:	n/a	chr7:27190942-27190955 chr7:27190847-27190856 chr7:27190353-27190362 chr7:27190348-27190368 chr7:27190349-27190367 chr7:27190354-27190368 chr7:27190348-27190368
22	MXI1	chr7:27189942-27190768	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr7:27189840-27189990	HRPEpiC	eye:	n/a	n/a
24	GTF2F1	chr7:27189779-27190875	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr7:27189822-27191130	HCT-116	colon:	n/a	n/a
26	MAZ	chr7:27189838-27190761	Hela-S3	cervix:	n/a	chr7:27190352-27190361
27	POLR2A	chr7:27189830-27190779	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr7:27189939-27191109	HCT-116	colon:	n/a	n/a
29	MXI1	chr7:27189952-27190870	HepG2	liver:	n/a	n/a
30	CTCF	chr7:27189840-27189990	NHEK	skin:	n/a	n/a
31	MAX	chr7:27189669-27191230	A549	lung:	n/a	chr7:27191106-27191115 chr7:27190352-27190361
32	POLR2A	chr7:27189767-27192854	HEK293	kidney:	n/a	n/a
33	SIN3AK20	chr7:27189961-27190862	PANC-1	pancreas:	n/a	n/a
34	POLR2A	chr7:27189944-27190629	HepG2	liver:	n/a	n/a
35	CHD2	chr7:27189979-27190804	Hela-S3	cervix:	n/a	n/a
36	SUZ12	chr7:27189808-27192571	H1-hESC	embryonic stem cell:	n/a	n/a
37	REST	chr7:27189981-27190686	ECC-1	luminal epithelium:	n/a	chr7:27190353-27190362 chr7:27190348-27190368 chr7:27190349-27190367 chr7:27190354-27190368 chr7:27190348-27190368
38	CTCF	chr7:27189880-27190030	HMEC	breast:	n/a	n/a
39	POLR2A	chr7:27189909-27190732	Hela-S3	cervix:	n/a	n/a
40	KAP1	chr7:27189979-27190521	HEK293	kidney:	n/a	n/a
41	CTCF	chr7:27189434-27191406	A549	lung:	n/a	chr7:27190138-27190151
42	CTCF	chr7:27189799-27191284	SK-N-SH	brain:	n/a	chr7:27190138-27190151
43	POLR2A	chr7:27189798-27190810	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr7:27189940-27190025	MCF-7	breast:	n/a	n/a
45	TCF7L2	chr7:27189940-27190995	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr7:27189703-27190867	Hela-S3	cervix:	n/a	n/a
47	RCOR1	chr7:27189900-27190786	Hela-S3	cervix:	n/a	n/a
48	SMC3	chr7:27189553-27191010	SK-N-SH	brain:	n/a	n/a
49	CTCF	chr7:27189860-27190010	SK-N-SH_RA	brain:	n/a	n/a
50	POLR2A	chr7:27189918-27191192	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	7:27082525-27089724..7:27181770-27195105	Hela-S3	cervix:
2	7:27181770-27195105..7:27230275-27238414	GM12878	blood:
3	7:27162022-27164727..7:27181770-27195105	H1-hESC	embryonic stem cell:	embryo
4	chr7:27181480..27183219-chr7:27189259..27191878,2	MCF-7	breast:
5	chr7:27184989..27187193-chr7:27189201..27192004,2	MCF-7	breast:
6	chr7:27181736..27184705-chr7:27188724..27191664,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EVX1-8	chr7:27189671-27191300	ENSG00000254369

Variant related genes	Relation type
HOXA6	TF binding region
ENSG00000106004	Chromatin interaction
ENSG00000254369	Chromatin interaction
ENSG00000106031	Chromatin interaction
ENSG00000213786	Chromatin interaction
ENSG00000253552	Chromatin interaction
ENSG00000243766	Chromatin interaction
ENSG00000253508	Chromatin interaction

Extended variants
information (count: 96 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10085570	0.85[CEU][hapmap];0.91[CHB][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs10225507	0.81[ASN][1000 genomes]
rs10238095	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10246712	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11564055	0.91[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs11762730	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11983200	0.93[JPT][hapmap];0.88[ASN][1000 genomes]
rs12530948	1.00[ASN][1000 genomes]
rs12533947	0.91[CHB][hapmap];0.92[JPT][hapmap];0.91[ASN][1000 genomes]
rs12666919	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12666926	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1548497	0.91[CHB][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs1725074	0.90[CHB][hapmap];0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs17449108	0.91[CHB][hapmap];0.92[JPT][hapmap];0.91[ASN][1000 genomes]
rs17471485	0.91[CHB][hapmap];0.92[JPT][hapmap];0.91[ASN][1000 genomes]
rs17471520	0.91[CHB][hapmap];0.92[JPT][hapmap];0.94[ASN][1000 genomes]
rs1801085	0.91[CHB][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs1859166	0.91[CHB][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs2107063	0.84[CEU][hapmap];0.91[CHB][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs2285722	0.90[ASN][1000 genomes]
rs2301720	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2301721	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2428432	0.91[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs2428433	0.91[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs2428434	0.91[CHB][hapmap];0.92[JPT][hapmap];0.90[ASN][1000 genomes]
rs2465275	0.91[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs2465276	0.91[CHB][hapmap];0.92[JPT][hapmap];0.90[ASN][1000 genomes]
rs3801320	0.93[ASN][1000 genomes]
rs3807597	0.85[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs3823764	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4722657	0.85[CEU][hapmap];0.91[CHB][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs4722659	0.85[CEU][hapmap];0.91[CHB][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs4722666	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61384251	0.90[ASN][1000 genomes]
rs6461985	0.91[CHB][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs6461987	0.91[CHB][hapmap];0.92[JPT][hapmap];0.94[ASN][1000 genomes]
rs68021164	0.97[ASN][1000 genomes]
rs6948297	0.91[CHB][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs6957209	0.91[CHB][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs6962314	0.94[ASN][1000 genomes]
rs6969780	0.91[CHB][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs6973182	0.91[CHB][hapmap];0.92[JPT][hapmap];0.94[ASN][1000 genomes]
rs6976129	0.82[CHB][hapmap];0.92[JPT][hapmap];0.94[ASN][1000 genomes]
rs73071548	0.93[ASN][1000 genomes]
rs73071550	0.93[ASN][1000 genomes]
rs7341470	0.85[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs739734	0.91[CHB][hapmap];0.92[JPT][hapmap];0.94[ASN][1000 genomes]
rs7798733	0.93[ASN][1000 genomes]
rs7801565	0.89[CHB][hapmap]
rs7811753	0.91[CHB][hapmap];0.92[JPT][hapmap]
rs875896	0.87[YRI][hapmap];0.86[AFR][1000 genomes]
rs875898	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs886339	0.83[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs929249	0.91[CHB][hapmap];0.92[JPT][hapmap];0.94[ASN][1000 genomes]
rs983184	1.00[CEU][hapmap];0.87[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs983185	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs983186	1.00[YRI][hapmap];0.96[AFR][1000 genomes]
rs985652	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:38 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025538	chr7:26482342-27376045	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
2	nsv538805	chr7:26482342-27376045	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
3	nsv1018709	chr7:26990384-27216552	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
4	nsv538806	chr7:26990384-27216552	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
5	nsv887856	chr7:27073731-27297791	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
6	nsv824038	chr7:27119294-27284522	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
7	nsv887857	chr7:27120689-27229549	Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
8	nsv824039	chr7:27121825-27294951	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
9	nsv824040	chr7:27121870-27295010	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
10	nsv887860	chr7:27127231-27196069	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
11	nsv887859	chr7:27127231-27196113	Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
12	nsv887861	chr7:27127231-27206688	Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
13	nsv887862	chr7:27127231-27217359	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
14	nsv887863	chr7:27127231-27243106	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
15	nsv887864	chr7:27127231-27243962	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
16	nsv887865	chr7:27127231-27247279	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
17	nsv887866	chr7:27127231-27248373	Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
18	nsv887867	chr7:27127231-27252246	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
19	nsv824041	chr7:27128039-27294951	Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
20	nsv887868	chr7:27135314-27202289	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
21	nsv887869	chr7:27135314-27297791	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
22	nsv887874	chr7:27136308-27196069	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
23	nsv1020608	chr7:27139892-27324004	Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
24	nsv538807	chr7:27139892-27324004	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
25	nsv1033316	chr7:27140645-27237951	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
26	nsv606465	chr7:27143757-27229549	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	174 gene(s)	inside rSNPs	diseases
27	nsv606466	chr7:27145024-27197319	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
28	nsv606467	chr7:27145100-27196113	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
29	nsv887875	chr7:27145100-27243962	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
30	nsv532118	chr7:27146920-27354205	Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
31	nsv5674	chr7:27152562-27197341	Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
32	nsv887876	chr7:27168858-27196069	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
33	nsv824042	chr7:27169231-27247232	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
34	nsv887877	chr7:27169388-27217359	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	115 gene(s)	inside rSNPs	diseases
35	nsv887878	chr7:27175295-27214557	Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	105 gene(s)	inside rSNPs	diseases
36	nsv887879	chr7:27175295-27297791	Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	151 gene(s)	inside rSNPs	diseases
37	esv1798853	chr7:27181568-27309266	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	150 gene(s)	inside rSNPs	diseases
38	nsv526526	chr7:27182142-27196113	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs3735530	HOTAIRM1	cis	Esophagus Muscularis	GTEx
rs3735530	HOXA2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27181800-27190400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
2	chr7:27183600-27190400	Flanking Active TSS	HUVEC	blood vessel
3	chr7:27186600-27191600	Flanking Active TSS	Adipose Nuclei	Adipose
4	chr7:27186600-27193000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
5	chr7:27186800-27190600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:27186800-27202600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr7:27187000-27190200	Flanking Active TSS	Primary hematopoietic stem cells	blood
8	chr7:27187000-27190200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
9	chr7:27187000-27190400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:27187200-27192400	Active TSS	Psoas Muscle	Psoas
11	chr7:27187400-27190800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
12	chr7:27187800-27190400	Flanking Active TSS	Osteobl	bone
13	chr7:27188000-27190000	Weak transcription	Gastric	stomach
14	chr7:27188000-27190200	Weak transcription	Right Atrium	heart
15	chr7:27188200-27190000	Bivalent/Poised TSS	Fetal Intestine Large	intestine
16	chr7:27188200-27190000	Weak transcription	Pancreas	Pancrea
17	chr7:27188400-27190200	Bivalent/Poised TSS	Fetal Stomach	stomach
18	chr7:27188400-27192400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr7:27188400-27192800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr7:27188600-27190200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr7:27188800-27190000	Bivalent/Poised TSS	Fetal Intestine Small	intestine
22	chr7:27188800-27192600	Active TSS	NHLF	lung
23	chr7:27189000-27190000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
24	chr7:27189000-27190000	Active TSS	Rectal Mucosa Donor 29	rectum
25	chr7:27189000-27190000	Enhancers	HSMMtube	muscle
26	chr7:27189000-27192600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr7:27189200-27190000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr7:27189200-27190400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:27189200-27190800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr7:27189200-27192600	Active TSS	NHDF-Ad	bronchial
31	chr7:27189400-27190000	Active TSS	Rectal Mucosa Donor 31	rectum
32	chr7:27189400-27190800	Active TSS	Fetal Kidney	kidney
33	chr7:27189400-27190800	Active TSS	Dnd41	blood
34	chr7:27189400-27190800	Active TSS	NHEK	skin
35	chr7:27189400-27191200	Active TSS	A549	lung
36	chr7:27189600-27190000	Flanking Active TSS	Colon Smooth Muscle	Colon
37	chr7:27189600-27190000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
38	chr7:27189600-27190200	Flanking Active TSS	Fetal Muscle Leg	muscle
39	chr7:27189600-27190600	Active TSS	Hela-S3	cervix
40	chr7:27189800-27190000	Flanking Bivalent TSS/Enh	HepG2	liver
41	chr7:27189800-27190000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
42	chr7:27189800-27190200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr7:27189800-27190200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
44	chr7:27189800-27190200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
45	chr7:27189800-27190200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
46	chr7:27189800-27190200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
47	chr7:27189800-27190200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr7:27189800-27190200	Flanking Bivalent TSS/Enh	Fetal Lung	lung
49	chr7:27189800-27190200	Bivalent Enhancer	Fetal Thymus	thymus
50	chr7:27189800-27190200	Flanking Active TSS	Rectal Smooth Muscle	rectum

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