Variant report

Variant	rs2863984
Chromosome Location	chr7:64314296-64314297
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TAL1	chr7:64314046-64314454	K562	blood:	n/a	n/a
2	TEAD4	chr7:64314023-64314340	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:64314295-64314345	PANC-1	pancreas:	n/a
2	chr7:64314295-64314345	HEK293	kidney:	embryo
3	chr7:64314295-64314345	AG10803	skin:	n/a
4	chr7:64314295-64314345	BJ	skin:	n/a
5	chr7:64314295-64314345	AG04450	lung:	fetal
6	chr7:64314295-64314345	SK-N-MC	brain:	n/a
7	chr7:64314295-64314345	ECC-1	luminal epithelium:	n/a
8	chr7:64314295-64314345	MCF10A-Er-Src	breast:	n/a
9	chr7:64314295-64314345	NB4	blood:	n/a
10	chr7:64314295-64314345	Jurkat	blood:	n/a
11	chr7:64314295-64314345	GM06990	blood:	n/a
12	chr7:64314295-64314345	GM12891	blood:	n/a
13	chr7:64314295-64314345	ovcar-3	ovarian:	n/a
14	chr7:64314295-64314345	GM19239	blood:	n/a
15	chr7:64314295-64314345	K562	blood:	n/a
16	chr7:64314295-64314345	Hepatocyte	liver:	n/a
17	chr7:64314295-64314345	HNPCEpiC	eye:	n/a
18	chr7:64314295-64314345	RPTEC	kidney:	n/a
19	chr7:64314295-64314345	MCF-7	breast:	n/a
20	chr7:64314295-64314345	NH-A	brain:	n/a
21	chr7:64314295-64314345	GM12892	blood:	n/a
22	chr7:64314295-64314345	HMEC	breast:	n/a
23	chr7:64314295-64314345	HRE	kidney:	n/a
24	chr7:64314295-64314345	AG09309	skin:	n/a
25	chr7:64314295-64314345	AoSMC	blood vessel:	n/a
26	chr7:64314295-64314345	Hela-S3	cervix:	n/a
27	chr7:64314295-64314345	HCM	heart:	n/a
28	chr7:64314295-64314345	SK-N-SH	brain:	n/a
29	chr7:64314295-64314345	A549	lung:	n/a
30	chr7:64314295-64314345	SK-N-SH_RA	brain:	n/a
31	chr7:64314295-64314345	LNCaP	prostate:	n/a
32	chr7:64314295-64314345	T-47D	breast:	n/a
33	chr7:64314295-64314345	PFSK-1	brain:	n/a
34	chr7:64314295-64314345	H1-hESC	embryonic stem cell:	embryo
35	chr7:64314295-64314345	HRPEpiC	eye:	n/a
36	chr7:64314295-64314345	GM12878	blood:	n/a
37	chr7:64314295-64314345	AG04449	skin:	fetal
38	chr7:64314295-64314345	HPAEpiC	pulmonary alveolar:	n/a
39	chr7:64314295-64314345	PrEC	prostate:	n/a
40	chr7:64314295-64314345	HIPEpiC	eye:	n/a
41	chr7:64314295-64314345	U87	brain:	n/a
42	chr7:64314295-64314345	HL-60	blood:	n/a
43	chr7:64314295-64314345	NHDF-neo	bronchial:	n/a
44	chr7:64314295-64314345	SKMC	muscle:	n/a
45	chr7:64314295-64314345	AG09319	gingival:	n/a
46	chr7:64314295-64314345	BE2_C	brain:	n/a
47	chr7:64314295-64314345	HRCEpiC	kidney:	n/a
48	chr7:64314295-64314345	HCF	heart:	n/a
49	chr7:64314295-64314345	ProgFib	skin:	n/a
50	chr7:64314295-64314345	HepG2	liver:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:64314139..64316583-chr7:64317085..64319810,2	K562	blood:
2	chr7:64314110..64316754-chr7:64405768..64408146,2	K562	blood:

No data

Variant related genes	Relation type
SEPHS1P1	TF binding region
SEPHS1P1	CpG island

Extended variants
information (count: 126 )
Associated
traits (count: 34 )

rSNPs within LD-proxies of this variant (count:110)

rs_ID	r²[population]
rs1002942	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10226807	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10231738	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10237833	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10245591	0.87[ASN][1000 genomes]
rs10255860	0.93[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10256484	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10258594	0.80[CEU][hapmap];0.81[EUR][1000 genomes]
rs10259858	0.93[CEU][hapmap];0.90[CHB][hapmap];0.89[JPT][hapmap];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10263876	0.93[CEU][hapmap];0.89[CHB][hapmap];0.94[JPT][hapmap];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10264026	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10265252	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10273821	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10273979	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10276867	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10277215	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10277498	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10277510	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10277525	0.81[ASN][1000 genomes]
rs10282599	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10429185	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10949950	0.93[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11766146	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11769995	0.84[EUR][1000 genomes]
rs11771842	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11772109	0.93[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11773236	0.93[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12154813	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12534485	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12668689	0.81[EUR][1000 genomes]
rs12672910	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13223080	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13233432	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13233552	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13239272	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13239921	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1524823	0.92[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1534147	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1568909	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1568910	0.93[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1568911	0.93[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1880657	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1969460	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2030811	0.92[CEU][hapmap];0.89[CHB][hapmap];0.94[JPT][hapmap];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2418466	0.86[ASN][1000 genomes]
rs2863924	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28871650	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34274096	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34401948	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34640216	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34808801	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34843623	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35037176	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35238187	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35332997	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35373826	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35740030	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3763507	0.93[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3813701	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4278061	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4398786	0.93[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4502993	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4717224	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4717225	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4717226	0.93[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4718149	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4718150	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4718151	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4718153	0.93[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4718158	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4718159	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4718160	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4718161	0.93[CEU][hapmap];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4718163	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs4718165	0.80[EUR][1000 genomes]
rs4718168	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4718171	0.96[CEU][hapmap];0.90[CHB][hapmap];0.89[JPT][hapmap];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6460201	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6460202	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6460203	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6460205	0.92[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6460206	0.93[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6460212	0.92[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs66496421	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs67268573	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6956037	0.93[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6957325	0.93[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6960979	0.81[EUR][1000 genomes]
rs6964268	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6974633	0.81[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs6975625	0.93[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6980403	0.83[EUR][1000 genomes]
rs73137833	0.83[ASN][1000 genomes]
rs7455565	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7777724	0.81[CEU][hapmap]
rs7785355	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7798270	0.93[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7799424	0.94[JPT][hapmap]
rs7802164	0.91[ASN][1000 genomes]
rs7804955	0.84[EUR][1000 genomes]
rs7808902	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7809122	0.96[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7810293	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs7810539	0.80[CEU][hapmap]
rs867630	0.82[CEU][hapmap]
rs871076	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs871077	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs884476	0.92[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs940887	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9886096	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422405	chr7:63709739-64632341	Enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
2	nsv427787	chr7:63741770-64419520	Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	esv2755057	chr7:63819849-64345822	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
4	nsv464518	chr7:63881238-64506904	Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv607312	chr7:63881238-64506904	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
6	nsv888274	chr7:63990100-64331123	Strong transcription ZNF genes & repeats Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
7	nsv888275	chr7:63990100-64468590	Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv888276	chr7:63990100-64511564	Strong transcription ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
9	nsv888279	chr7:64094285-64331123	Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
10	nsv1022042	chr7:64226499-64566945	Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
11	nsv1026390	chr7:64240323-64414364	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
12	nsv1033291	chr7:64273434-64406276	Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
13	nsv508457	chr7:64286522-64391112	Strong transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
14	esv1797468	chr7:64296309-64356050	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	nsv888282	chr7:64299645-64511564	Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
16	nsv436564	chr7:64313936-64318911	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:34)

SNP	Gene	Cis/trans	Tissue	Source
rs2863984	RP11-797H7.5	cis	Adipose Subcutaneous	GTEx
rs2863984	RP11-460N20.5	cis	Thyroid	GTEx
rs2863984	RP11-797H7.3	cis	Esophagus Mucosa	GTEx
rs2863984	RP11-797H7.3	cis	Whole Blood	GTEx
rs2863984	RP11-797H7.3	cis	Thyroid	GTEx
rs2863984	RP11-797H7.5	cis	Nerve Tibial	GTEx
rs2863984	RP11-797H7.3	cis	Esophagus Muscularis	GTEx
rs2863984	RP11-797H7.3	cis	Artery Tibial	GTEx
rs2863984	SEPHS1P1	cis	Thyroid	GTEx
rs2863984	RP11-797H7.5	cis	Artery Tibial	GTEx
rs2863984	RP11-797H7.3	cis	Nerve Tibial	GTEx
rs2863984	RP11-667F9.1	cis	Adipose Subcutaneous	GTEx
rs2863984	ZNF273	cis	Esophagus Mucosa	GTEx
rs2863984	RP11-460N20.5	cis	Adipose Subcutaneous	GTEx
rs2863984	INTS4L1	cis	Skin Sun Exposed Lower leg	GTEx
rs2863984	RP11-797H7.3	cis	Muscle Skeletal	GTEx
rs2863984	RP11-460N20.5	cis	Artery Tibial	GTEx
rs2863984	SEPHS1P1	cis	Nerve Tibial	GTEx
rs2863984	RP11-797H7.5	cis	Heart Left Ventricle	GTEx
rs2863984	RP11-797H7.3	cis	Skin Sun Exposed Lower leg	GTEx
rs2863984	RP11-797H7.3	cis	Heart Left Ventricle	GTEx
rs2863984	RP11-797H7.3	cis	Artery Aorta	GTEx
rs2863984	SEPHS1P1	cis	Artery Tibial	GTEx
rs2863984	AC104057.1	cis	Adipose Subcutaneous	GTEx
rs2863984	ZNF273	cis	Heart Left Ventricle	GTEx
rs2863984	RP11-797H7.5	cis	lung	GTEx
rs2863984	RP11-797H7.5	cis	Esophagus Muscularis	GTEx
rs2863984	RP11-797H7.3	cis	Adipose Subcutaneous	GTEx
rs2863984	RP11-797H7.5	cis	Thyroid	GTEx
rs2863984	RP11-667F9.1	cis	Nerve Tibial	GTEx
rs2863984	RP11-797H7.3	cis	lung	GTEx
rs2863984	SEPHS1P1	cis	Skin Sun Exposed Lower leg	GTEx
rs2863984	RP11-460N20.5	cis	Whole Blood	GTEx
rs2863984	SEPHS1P1	cis	Esophagus Muscularis	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:64310400-64320600	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr7:64311600-64314600	Weak transcription	Stomach Smooth Muscle	stomach

The 2.0 version of rSNPBase

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