Variant report

Variant	rs3806234
Chromosome Location	chr1:153631071-153631072
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:441)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAFK	chr1:153630976-153631320	Hela-S3	cervix:	n/a	chr1:153631117-153631128
2	TRIM28	chr1:153630794-153631332	K562	blood:	n/a	n/a
3	STAT3	chr1:153630957-153631345	MCF10A-Er-Src	breast:	n/a	chr1:153631090-153631098 chr1:153631088-153631099 chr1:153631083-153631104 chr1:153631084-153631104 chr1:153631058-153631070 chr1:153631146-153631158 chr1:153631087-153631101
4	MXI1	chr1:153630870-153631493	GM12878	blood:	n/a	n/a
5	TAF1	chr1:153631025-153631407	H1-hESC	embryonic stem cell:	n/a	n/a
6	YY1	chr1:153630927-153631537	GM12892	blood:	n/a	n/a
7	SIN3A	chr1:153630964-153631903	H1-hESC	embryonic stem cell:	n/a	chr1:153631150-153631161
8	CREB1	chr1:153631004-153631229	A549	lung:	n/a	n/a
9	POLR2A	chr1:153630830-153631559	HUVEC	blood vessel:	n/a	n/a
10	SIN3AK20	chr1:153630945-153631609	SK-N-SH	brain:	n/a	n/a
11	PML	chr1:153630874-153631519	K562	blood:	n/a	n/a
12	CEBPB	chr1:153630955-153631285	Hela-S3	cervix:	n/a	n/a
13	TAF1	chr1:153630965-153631406	SK-N-SH	brain:	n/a	n/a
14	CTCF	chr1:153631040-153631190	GM12875	blood:	n/a	n/a
15	TAF1	chr1:153631071-153631383	GM12891	blood:	n/a	n/a
16	CTCF	chr1:153631060-153631210	K562	blood:	n/a	n/a
17	SMC3	chr1:153630962-153631423	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr1:153630901-153631303	H1-hESC	embryonic stem cell:	n/a	chr1:153630922-153630930
19	PAX5	chr1:153631024-153631446	GM12892	blood:	n/a	n/a
20	CREB1	chr1:153630926-153631287	ECC-1	luminal epithelium:	n/a	n/a
21	GTF2F1	chr1:153630952-153631271	K562	blood:	n/a	n/a
22	CTCF	chr1:153631040-153631190	HMF	breast:	n/a	n/a
23	HMGN3	chr1:153630989-153631492	K562	blood:	n/a	n/a
24	YY1	chr1:153630848-153631505	A549	lung:	n/a	n/a
25	NFIC	chr1:153630875-153631242	HepG2	liver:	n/a	n/a
26	ZNF263	chr1:153630853-153631915	HEK293-T-REx	kidney:	n/a	chr1:153631057-153631066
27	CREB1	chr1:153631014-153631375	H1-hESC	embryonic stem cell:	n/a	n/a
28	E2F4	chr1:153630959-153631392	K562	blood:	n/a	n/a
29	POLR2A	chr1:153631027-153631590	GM10847	blood:	n/a	n/a
30	POLR2A	chr1:153630871-153631726	Hela-S3	cervix:	n/a	n/a
31	MAX	chr1:153630897-153631413	K562	blood:	n/a	n/a
32	CTCF	chr1:153631060-153631210	BE2_C	brain:	n/a	n/a
33	POLR2A	chr1:153630757-153632015	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr1:153630882-153631802	U87	brain:	n/a	n/a
35	MTA3	chr1:153630712-153631896	GM12878	blood:	n/a	n/a
36	CHD2	chr1:153630974-153631279	K562	blood:	n/a	chr1:153631061-153631071
37	CTCF	chr1:153631040-153631190	AG04449	skin:	n/a	n/a
38	SIN3A	chr1:153631050-153631590	GM12878	blood:	n/a	chr1:153631150-153631161
39	E2F6	chr1:153630970-153631193	K562	blood:	n/a	n/a
40	RUNX3	chr1:153630798-153631399	GM12878	blood:	n/a	n/a
41	CTCF	chr1:153630974-153631270	GM12878	blood:	n/a	n/a
42	USF1	chr1:153631010-153631475	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr1:153631040-153631190	HMEC	breast:	n/a	n/a
44	ELF1	chr1:153630925-153631249	A549	lung:	n/a	n/a
45	POLR2A	chr1:153630893-153631973	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr1:153630295-153631965	HepG2	liver:	n/a	n/a
47	USF2	chr1:153631000-153631380	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr1:153631040-153631190	HFF-Myc	foreskin:	n/a	n/a
49	POLR2A	chr1:153630977-153631415	A549	lung:	n/a	n/a
50	USF1	chr1:153630925-153631540	ECC-1	luminal epithelium:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:153631048-153631098	HCM	heart:	n/a
2	chr1:153631048-153631098	NH-A	brain:	n/a
3	chr1:153631048-153631098	NHDF-neo	bronchial:	n/a
4	chr1:153631048-153631098	HRPEpiC	eye:	n/a
5	chr1:153631048-153631098	HCPEpiC	choroid plexus:	n/a
6	chr1:153631048-153631098	NB4	blood:	n/a
7	chr1:153631048-153631098	CMK	blood:	n/a
8	chr1:153631048-153631098	MCF10A-Er-Src	breast:	n/a
9	chr1:153631048-153631098	HIPEpiC	eye:	n/a
10	chr1:153631048-153631098	LNCaP	prostate:	n/a
11	chr1:153631048-153631098	PANC-1	pancreas:	n/a
12	chr1:153631048-153631098	Hela-S3	cervix:	n/a
13	chr1:153631048-153631098	AG10803	skin:	n/a
14	chr1:153631048-153631098	PFSK-1	brain:	n/a
15	chr1:153631048-153631098	SK-N-SH_RA	brain:	n/a
16	chr1:153631048-153631098	HCF	heart:	n/a
17	chr1:153631048-153631098	NT2-D1	testis:	n/a
18	chr1:153631048-153631098	GM12878	blood:	n/a
19	chr1:153631048-153631098	HRE	kidney:	n/a
20	chr1:153631048-153631098	HepG2	liver:	n/a
21	chr1:153631048-153631098	AG09309	skin:	n/a
22	chr1:153631048-153631098	K562	blood:	n/a
23	chr1:153631048-153631098	H1-hESC	embryonic stem cell:	embryo
24	chr1:153631048-153631098	HEK293	kidney:	embryo
25	chr1:153631048-153631098	Hepatocyte	liver:	n/a
26	chr1:153631048-153631098	BJ	skin:	n/a
27	chr1:153631048-153631098	ovcar-3	ovarian:	n/a
28	chr1:153631048-153631098	ECC-1	luminal epithelium:	n/a
29	chr1:153631048-153631098	SAEC	small airway:	n/a
30	chr1:153631048-153631098	IMR90	lung:	fetal
31	chr1:153631048-153631098	AoSMC	blood vessel:	n/a
32	chr1:153631048-153631098	HRCEpiC	kidney:	n/a
33	chr1:153631048-153631098	RPTEC	kidney:	n/a
34	chr1:153631048-153631098	GM12891	blood:	n/a
35	chr1:153631048-153631098	AG04449	skin:	fetal
36	chr1:153631048-153631098	ProgFib	skin:	n/a
37	chr1:153631048-153631098	SK-N-MC	brain:	n/a
38	chr1:153631048-153631098	Caco-2	colon:	n/a
39	chr1:153631048-153631098	NHBE	bronchial:	n/a
40	chr1:153631048-153631098	SK-N-SH	brain:	n/a
41	chr1:153631048-153631098	Jurkat	blood:	n/a
42	chr1:153631048-153631098	HL-60	blood:	n/a
43	chr1:153631048-153631098	U87	brain:	n/a
44	chr1:153631048-153631098	GM12892	blood:	n/a
45	chr1:153631048-153631098	GM19239	blood:	n/a
46	chr1:153631048-153631098	BE2_C	brain:	n/a
47	chr1:153631048-153631098	GM06990	blood:	n/a
48	chr1:153631048-153631098	HMEC	breast:	n/a
49	chr1:153631048-153631098	AG09319	gingival:	n/a
50	chr1:153631048-153631098	HEEpiC	esophagus:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:153579256..153583611-chr1:153630358..153635573,4	MCF-7	breast:
2	chr1:153605696..153608522-chr1:153629929..153633320,6	MCF-7	breast:
3	chr1:153629862..153632577-chr1:153659473..153661704,3	MCF-7	breast:
4	chr1:153597855..153601076-chr1:153629883..153633781,4	MCF-7	breast:
5	chr1:153629459..153632821-chr1:153961630..153966753,5	K562	blood:
6	chr1:153584270..153586809-chr1:153629991..153631660,2	MCF-7	breast:

No data

Variant related genes	Relation type
SNAPIN	TF binding region
SNAPIN	CpG island
ENSG00000272030	Chromatin interaction
ENSG00000160678	Chromatin interaction
ENSG00000177954	Chromatin interaction
ENSG00000271853	Chromatin interaction
ENSG00000189171	Chromatin interaction
ENSG00000188643	Chromatin interaction
ENSG00000169418	Chromatin interaction
ENSG00000160679	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 15 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1046381	0.83[ASN][1000 genomes]
rs10797056	0.90[CHD][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs10797090	0.88[ASN][1000 genomes]
rs10797096	0.92[ASW][hapmap];0.95[CHB][hapmap];0.90[CHD][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];1.00[MKK][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10908746	0.83[ASN][1000 genomes]
rs10908848	0.95[CHB][hapmap];0.94[JPT][hapmap];0.81[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs11265625	0.90[CHB][hapmap];0.86[CHD][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];0.88[LWK][hapmap];0.84[MEX][hapmap];0.87[TSI][hapmap];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11265633	0.83[ASN][1000 genomes]
rs11588347	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12139953	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12564925	0.90[CHD][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs12730186	0.93[ASN][1000 genomes]
rs1888115	0.90[CHD][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs2274739	0.90[CHD][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs2274740	0.90[CHD][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs28379831	0.83[ASN][1000 genomes]
rs28380060	0.90[CHD][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs28518786	0.87[ASN][1000 genomes]
rs28580554	0.90[CHD][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs28700217	0.83[ASN][1000 genomes]
rs3790411	0.90[CHD][hapmap];0.88[JPT][hapmap]
rs3790412	0.90[CHD][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs3795396	0.90[CHB][hapmap];0.93[CHD][hapmap];0.85[ASN][1000 genomes]
rs3806233	0.83[CHD][hapmap]
rs3818632	0.90[CHD][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs3828031	0.90[CHD][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs3862047	0.92[ASW][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];1.00[MKK][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4351684	0.90[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs4515830	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs4845557	0.83[ASN][1000 genomes]
rs4845563	0.92[ASW][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];1.00[MKK][hapmap];0.85[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4845564	0.87[ASN][1000 genomes]
rs55772653	0.82[AFR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6427640	0.92[ASN][1000 genomes]
rs66721814	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6674929	0.92[ASW][hapmap];0.95[CHB][hapmap];0.90[CHD][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];0.96[LWK][hapmap];0.84[MEX][hapmap];1.00[MKK][hapmap];0.87[TSI][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7345	0.90[CHB][hapmap];0.96[CHD][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs7934	0.90[CHD][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs913860	0.85[CHB][hapmap];0.86[CHD][hapmap]
rs913861	0.80[CHD][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs9661993	0.80[ASN][1000 genomes]
rs9662664	0.90[CHB][hapmap];0.83[CHD][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];0.80[MEX][hapmap];0.87[TSI][hapmap];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010488	chr1:152901263-153670972	Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
2	nsv535171	chr1:152901263-153670972	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
3	nsv547928	chr1:153612133-153714252	Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	esv2830411	chr1:153613393-153725007	Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
5	nsv1067771	chr1:153613593-153724866	Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
6	nsv530052	chr1:153613593-153724866	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
7	nsv1005818	chr1:153613597-153724980	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
8	nsv535173	chr1:153613597-153724980	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
9	nsv1007835	chr1:153613597-153729959	Genic enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
10	nsv535174	chr1:153613597-153729959	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
11	nsv1011897	chr1:153613597-153836703	Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
12	nsv464028	chr1:153622220-153723037	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
13	nsv547929	chr1:153622220-153723037	Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
14	nsv999364	chr1:153622634-154419436	Strong transcription Genic enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	286 gene(s)	inside rSNPs	diseases
15	nsv535175	chr1:153622634-154419436	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	286 gene(s)	inside rSNPs	diseases
16	nsv1001312	chr1:153622834-153724867	Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
17	nsv535176	chr1:153622834-153724867	Active TSS Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases

mRNA abundance (count:15)

SNP	Gene	Cis/trans	Tissue	Source
rs3806234	S100A9	cis	parietal	SCAN
rs3806234	S100A13	Cis_1M	lymphoblastoid	RTeQTL
rs3806234	S100A16	cis	cerebellum	SCAN
rs3806234	LCE2D	cis	cerebellum	SCAN
rs3806234	S100A10	cis	cerebellum	SCAN
rs3806234	RP1-178F15.4	cis	Muscle Skeletal	GTEx
rs3806234	S100A13	cis	multi-tissue	Pritchard
rs3806234	S100A13	cis	parietal	SCAN
rs3806234	RP1-178F15.4	cis	Adipose Subcutaneous	GTEx
rs3806234	CA14	cis	parietal	SCAN
rs3806234	S100A13	cis	lymphoblastoid	seeQTL
rs3806234	S100A2	cis	cerebellum	SCAN
rs3806234	S100A4	cis	lymphoblastoid	seeQTL
rs3806234	S100A16	cis	parietal	SCAN
rs3806234	FLG	cis	cerebellum	SCAN

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153618400-153631200	Weak transcription	Aorta	Aorta
2	chr1:153624600-153631200	Weak transcription	Gastric	stomach
3	chr1:153630400-153631600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr1:153630400-153631600	Active TSS	Brain Angular Gyrus	brain
5	chr1:153630400-153631600	Active TSS	Skeletal Muscle Female	skeletal muscle
6	chr1:153630400-153631800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
7	chr1:153630400-153631800	Active TSS	Rectal Mucosa Donor 29	rectum
8	chr1:153630600-153631200	Flanking Active TSS	Primary B cells from cord blood	blood
9	chr1:153630600-153631600	Active TSS	Duodenum Mucosa	Duodenum
10	chr1:153630600-153631600	Active TSS	Duodenum Smooth Muscle	Duodenum
11	chr1:153630600-153631600	Active TSS	Rectal Smooth Muscle	rectum
12	chr1:153630600-153631600	Active TSS	Stomach Smooth Muscle	stomach
13	chr1:153630600-153631800	Active TSS	Colon Smooth Muscle	Colon
14	chr1:153630600-153632000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:153630600-153632400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr1:153630800-153631200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:153630800-153631200	Enhancers	Fetal Brain Male	brain
18	chr1:153630800-153631200	Flanking Active TSS	Fetal Muscle Leg	muscle
19	chr1:153630800-153631400	Active TSS	HepG2	liver
20	chr1:153630800-153631600	Active TSS	H1 Cell Line	embryonic stem cell
21	chr1:153630800-153631600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
22	chr1:153630800-153631600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr1:153630800-153631600	Active TSS	Liver	Liver
24	chr1:153630800-153631600	Active TSS	Brain Hippocampus Middle	brain
25	chr1:153630800-153631600	Active TSS	Rectal Mucosa Donor 31	rectum
26	chr1:153630800-153631800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr1:153630800-153631800	Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr1:153630800-153631800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr1:153630800-153631800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr1:153630800-153631800	Active TSS	Brain Anterior Caudate	brain
31	chr1:153630800-153631800	Active TSS	Brain Germinal Matrix	brain
32	chr1:153630800-153631800	Active TSS	Brain Substantia Nigra	brain
33	chr1:153630800-153631800	Active TSS	Fetal Heart	heart
34	chr1:153630800-153631800	Active TSS	Fetal Lung	lung
35	chr1:153630800-153631800	Active TSS	Fetal Stomach	stomach
36	chr1:153630800-153631800	Active TSS	Right Atrium	heart
37	chr1:153630800-153631800	Active TSS	Right Ventricle	heart
38	chr1:153630800-153631800	Active TSS	Stomach Mucosa	stomach
39	chr1:153630800-153631800	Active TSS	HSMM	muscle
40	chr1:153630800-153632000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr1:153630800-153632000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
42	chr1:153630800-153632000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
43	chr1:153630800-153632000	Active TSS	Left Ventricle	heart
44	chr1:153630800-153632000	Active TSS	HSMMtube	muscle
45	chr1:153630800-153632200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr1:153630800-153632200	Active TSS	Psoas Muscle	Psoas
47	chr1:153630800-153632400	Active TSS	HUES48 Cell Line	embryonic stem cell
48	chr1:153630800-153632400	Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr1:153630800-153632400	Active TSS	HUES64 Cell Line	embryonic stem cell
50	chr1:153630800-153632600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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