Variant report

Variant	rs6969584
Chromosome Location	chr7:100209747-100209748
allele	A/C
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	POLR2A	chr7:100209451-100210290	HepG2	liver:	n/a	n/a
2	EBF1	chr7:100209646-100210021	GM12878	blood:	n/a	n/a
3	CREB1	chr7:100209485-100210047	H1-hESC	embryonic stem cell:	n/a	chr7:100209653-100209666
4	TCF3	chr7:100209683-100210077	GM12878	blood:	n/a	n/a
5	TCF7L2	chr7:100209453-100210165	PANC-1	pancreas:	n/a	n/a
6	POLR2A	chr7:100209263-100210451	K562	blood:	n/a	n/a
7	MAX	chr7:100209397-100210989	MCF-7	breast:	n/a	n/a
8	YY1	chr7:100209428-100210221	SK-N-SH	brain:	n/a	chr7:100209600-100209609
9	CHD1	chr7:100209544-100210012	GM12878	blood:	n/a	n/a
10	GABPA	chr7:100209614-100210180	HepG2	liver:	n/a	chr7:100210008-100210017
11	PML	chr7:100209340-100210279	GM12878	blood:	n/a	n/a
12	POLR2A	chr7:100209452-100210289	MCF10A-Er-Src	breast:	n/a	n/a
13	POU2F2	chr7:100209683-100210148	GM12891	blood:	n/a	chr7:100210002-100210014 chr7:100209997-100210009
14	CHD2	chr7:100209534-100210300	GM12878	blood:	n/a	chr7:100210060-100210070
15	POLR2A	chr7:100209361-100210391	SK-N-MC	brain:	n/a	n/a
16	MAZ	chr7:100209490-100210303	K562	blood:	n/a	n/a
17	E2F4	chr7:100209490-100210288	MCF10A-Er-Src	breast:	n/a	chr7:100209672-100209681 chr7:100209992-100210002 chr7:100209600-100209609
18	CHD2	chr7:100209662-100209929	HepG2	liver:	n/a	n/a
19	EP300	chr7:100209479-100210056	GM12878	blood:	n/a	chr7:100209999-100210015
20	CREB1	chr7:100209522-100209809	A549	lung:	n/a	chr7:100209653-100209666
21	POLR2A	chr7:100209409-100210392	Raji	blood:	n/a	n/a
22	MXI1	chr7:100209542-100210314	HepG2	liver:	n/a	n/a
23	ELF1	chr7:100209547-100210169	HepG2	liver:	n/a	chr7:100209778-100209791
24	SRF	chr7:100209654-100209945	GM12878	blood:	n/a	n/a
25	SP2	chr7:100209544-100209846	K562	blood:	n/a	n/a
26	SIX5	chr7:100209667-100209931	A549	lung:	n/a	n/a
27	CUX1	chr7:100209497-100210057	K562	blood:	n/a	n/a
28	MYC	chr7:100209373-100210290	NB4	blood:	n/a	n/a
29	ELF1	chr7:100209459-100210159	A549	lung:	n/a	chr7:100209778-100209791
30	POLR2A	chr7:100209555-100210187	GM10847	blood:	n/a	n/a
31	CREB1	chr7:100209401-100210234	H1-hESC	embryonic stem cell:	n/a	chr7:100209653-100209666
32	ZNF143	chr7:100209606-100210023	Hela-S3	cervix:	n/a	n/a
33	STAT3	chr7:100209521-100209905	GM12878	blood:	n/a	chr7:100209570-100209578
34	NFYB	chr7:100209454-100210099	K562	blood:	n/a	chr7:100209758-100209773 chr7:100209670-100209685 chr7:100209758-100209772 chr7:100209670-100209684 chr7:100209757-100209769 chr7:100209670-100209685 chr7:100209667-100209682 chr7:100209758-100209773 chr7:100209760-100209770
35	FOXP2	chr7:100209599-100210286	PFSK-1	brain:	n/a	n/a
36	PML	chr7:100209391-100210232	K562	blood:	n/a	n/a
37	CREB1	chr7:100209440-100210425	GM12878	blood:	n/a	chr7:100209653-100209666
38	ELK4	chr7:100209546-100210109	Hela-S3	cervix:	n/a	chr7:100209781-100209792
39	POLR2A	chr7:100209364-100210355	ECC-1	luminal epithelium:	n/a	n/a
40	RCOR1	chr7:100209468-100210092	GM12878	blood:	n/a	n/a
41	JUN	chr7:100209423-100210548	K562	blood:	n/a	chr7:100209654-100209667 chr7:100210075-100210084
42	POLR2A	chr7:100209473-100210568	PFSK-1	brain:	n/a	n/a
43	SIN3AK20	chr7:100209665-100210485	K562	blood:	n/a	n/a
44	WRNIP1	chr7:100209502-100209992	GM12878	blood:	n/a	n/a
45	MYBL2	chr7:100209375-100210182	HepG2	liver:	n/a	n/a
46	RFX5	chr7:100209469-100210185	GM12878	blood:	n/a	n/a
47	SP1	chr7:100209443-100210256	K562	blood:	n/a	chr7:100209599-100209609 chr7:100210075-100210087 chr7:100209759-100209780 chr7:100210075-100210087 chr7:100210157-100210167 chr7:100210076-100210085 chr7:100209599-100209608 chr7:100210077-100210086 chr7:100210072-100210086 chr7:100209598-100209610 chr7:100210157-100210167 chr7:100209600-100209609 chr7:100209598-100209610 chr7:100209671-100209692 chr7:100209599-100209608 chr7:100209599-100209609 chr7:100210077-100210086
48	POLR2A	chr7:100209631-100210030	HepG2	liver:	n/a	n/a
49	STAT5A	chr7:100209364-100210070	GM12878	blood:	n/a	chr7:100209570-100209578
50	POLR2A	chr7:100209439-100210246	GM12892	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:100208313..100211642-chr7:100274412..100277175,3	MCF-7	breast:
2	chr7:100208281..100211057-chr7:100227699..100229748,2	K562	blood:
3	chr7:100208537..100210261-chr7:100463099..100465535,2	MCF-7	breast:
4	chr7:100199763..100200426-chr7:100209123..100210066,2	K562	blood:
5	chr7:45025529..45026232-chr7:100209353..100210277,2	NB4	blood:
6	chr7:100208330..100211092-chr7:100239329..100241095,2	MCF-7	breast:
7	chr7:100026802..100029460-chr7:100209697..100211823,3	MCF-7	breast:
8	chr7:100209659..100211246-chr7:100224414..100227276,2	MCF-7	breast:
9	chr7:100208130..100210288-chr7:100223518..100226835,3	MCF-7	breast:
10	chr7:100208465..100211590-chr7:100485559..100488810,4	MCF-7	breast:
11	chr7:100207856..100214217-chr7:100235772..100240956,9	K562	blood:
12	chr7:100025028..100029218-chr7:100206824..100213289,7	K562	blood:
13	chr7:100207401..100210043-chr7:100303952..100305930,2	K562	blood:
14	chr2:55276176..55276756-chr7:100209468..100210247,2	Hela-S3	cervix:
15	chr7:100206101..100213131-chr7:100214394..100226559,23	K562	blood:
16	chr7:100208147..100211165-chr7:100422696..100426389,3	MCF-7	breast:
17	chr7:100025645..100028263-chr7:100208101..100209907,2	K562	blood:
18	chr7:100209591..100210113-chr9:2844054..2844824,2	NB4	blood:
19	chr7:100208530..100211610-chr7:100269581..100272676,5	K562	blood:
20	chr7:100208147..100211505-chr7:100280175..100284290,3	MCF-7	breast:
21	chr7:100183793..100184708-chr7:100209218..100210071,2	K562	blood:
22	chr19:1103998..1104596-chr7:100209663..100210316,2	Hela-S3	cervix:
23	chr7:100207807..100212872-chr7:100269575..100273736,11	MCF-7	breast:
24	chr12:49075515..49076182-chr7:100209563..100210466,2	Hela-S3	cervix:
25	chr7:100208069..100211610-chr7:100269776..100275197,5	K562	blood:
26	chr7:100024499..100027894-chr7:100208680..100211740,5	MCF-7	breast:
27	chr7:100207856..100215304-chr7:100235701..100242038,10	K562	blood:
28	chr7:100208328..100213557-chr7:100269728..100273649,8	MCF-7	breast:
29	chr7:100182175..100185247-chr7:100208524..100211802,7	K562	blood:
30	chr12:120728933..120729810-chr7:100209484..100210054,2	Hela-S3	cervix:
31	chr7:100209391..100211157-chr7:100240305..100242617,2	MCF-7	breast:
32	chr7:100199287..100203860-chr7:100204915..100211773,14	MCF-7	breast:
33	chr7:100209668..100211370-chr7:100302058..100304907,3	K562	blood:
34	chr4:178230369..178231317-chr7:100209277..100209843,2	NB4	blood:
35	chr7:100180934..100186212-chr7:100208003..100211666,10	K562	blood:
36	chr7:100181910..100186072-chr7:100207984..100213440,10	MCF-7	breast:

Variant related genes	Relation type
MOSPD3	TF binding region
ENSG00000106333	Chromatin interaction
ENSG00000202538	Chromatin interaction
ENSG00000176125	Chromatin interaction
ENSG00000087087	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000146830	Chromatin interaction
ENSG00000224729	Chromatin interaction
ENSG00000146828	Chromatin interaction
ENSG00000106336	Chromatin interaction
ENSG00000196411	Chromatin interaction
ENSG00000172354	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000232956	Chromatin interaction
ENSG00000115310	Chromatin interaction
ENSG00000139620	Chromatin interaction
ENSG00000106327	Chromatin interaction
ENSG00000172336	Chromatin interaction
ENSG00000077454	Chromatin interaction
ENSG00000109674	Chromatin interaction
ENSG00000080608	Chromatin interaction
ENSG00000167468	Chromatin interaction
ENSG00000087077	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10487157	1.00[ASW][hapmap];1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10953298	0.96[ASN][1000 genomes]
rs11520986	0.85[MEX][hapmap]
rs11764045	1.00[ASW][hapmap];1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11766643	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11767547	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11770389	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11974395	0.84[MEX][hapmap]
rs11979818	0.85[MEX][hapmap]
rs11983334	0.84[MEX][hapmap]
rs11983745	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12532878	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13227444	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2075671	0.89[MEX][hapmap]
rs2075672	0.86[JPT][hapmap]
rs2075674	0.82[ASW][hapmap];0.88[CEU][hapmap];0.89[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.96[TSI][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2231170	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs2231172	0.84[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.85[TSI][hapmap]
rs28584500	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs41303510	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4727459	0.85[MEX][hapmap]
rs4729597	0.86[JPT][hapmap]
rs4729601	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs4729602	0.89[MEX][hapmap]
rs4729606	0.80[MEX][hapmap]
rs62482237	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62482238	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62482239	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62482242	0.84[AMR][1000 genomes]
rs6958696	0.83[AMR][1000 genomes]
rs6969697	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73156234	0.83[AMR][1000 genomes]
rs73407376	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7385804	0.86[JPT][hapmap]
rs7457024	0.96[ASN][1000 genomes]
rs7786877	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7812123	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7812235	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
2	nsv888777	chr7:100014711-100221867	Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
3	nsv888778	chr7:100014711-100236593	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	310 gene(s)	inside rSNPs	diseases
4	nsv888779	chr7:100014711-100313420	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	321 gene(s)	inside rSNPs	diseases
5	nsv888782	chr7:100064719-100236593	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
6	nsv888785	chr7:100141861-100313420	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
7	nsv888786	chr7:100159567-100313420	Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
8	nsv831072	chr7:100162503-100362835	Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
9	nsv5868	chr7:100169998-100214646	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	59 gene(s)	inside rSNPs	diseases
10	nsv888790	chr7:100200674-100232387	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	37 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs6969584	MOSPD3	cis	Whole Blood	GTEx
rs6969584	LHFPL3	cis	cerebellum	SCAN
rs6969584	POLR2J	cis	parietal	SCAN
rs6969584	SERPINE1	cis	cerebellum	SCAN
rs6969584	DLX5	cis	cerebellum	SCAN

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100203800-100209800	Weak transcription	Spleen	Spleen
2	chr7:100205400-100209800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:100208200-100210200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:100208600-100210800	Active TSS	Fetal Brain Female	brain
5	chr7:100208800-100210200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr7:100208800-100210400	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr7:100208800-100210400	Active TSS	Duodenum Mucosa	Duodenum
8	chr7:100208800-100210600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr7:100209000-100210200	Active TSS	Primary hematopoietic stem cells short term culture	blood
10	chr7:100209000-100210200	Active TSS	Brain Germinal Matrix	brain
11	chr7:100209000-100210400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:100209000-100210400	Active TSS	Colonic Mucosa	Colon
13	chr7:100209000-100210400	Active TSS	Rectal Mucosa Donor 29	rectum
14	chr7:100209000-100210600	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr7:100209000-100210600	Active TSS	Brain Angular Gyrus	brain
16	chr7:100209000-100210600	Active TSS	GM12878-XiMat	blood
17	chr7:100209000-100210800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr7:100209000-100211000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:100209000-100211000	Active TSS	Rectal Smooth Muscle	rectum
20	chr7:100209200-100209800	Active TSS	Primary B cells from cord blood	blood
21	chr7:100209200-100209800	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
22	chr7:100209200-100209800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:100209200-100210000	Active TSS	Fetal Heart	heart
24	chr7:100209200-100210000	Active TSS	Right Atrium	heart
25	chr7:100209200-100210200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr7:100209200-100210200	Active TSS	Liver	Liver
27	chr7:100209200-100210200	Active TSS	Fetal Muscle Trunk	muscle
28	chr7:100209200-100210200	Active TSS	Placenta	Placenta
29	chr7:100209200-100210200	Active TSS	Skeletal Muscle Male	skeletal muscle
30	chr7:100209200-100210200	Active TSS	Dnd41	blood
31	chr7:100209200-100210200	Active TSS	HMEC	breast
32	chr7:100209200-100210400	Active TSS	Primary B cells from peripheral blood	blood
33	chr7:100209200-100210400	Active TSS	Primary T cells from cord blood	blood
34	chr7:100209200-100210400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
35	chr7:100209200-100210400	Active TSS	Primary T helper cells PMA-I stimulated	--
36	chr7:100209200-100210400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr7:100209200-100210400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
38	chr7:100209200-100210400	Active TSS	Primary T killer memory cells from peripheral blood	blood
39	chr7:100209200-100210400	Active TSS	Cortex derived primary cultured neurospheres	brain
40	chr7:100209200-100210400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:100209200-100210400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr7:100209200-100210400	Active TSS	Adipose Nuclei	Adipose
43	chr7:100209200-100210400	Active TSS	Brain Hippocampus Middle	brain
44	chr7:100209200-100210400	Active TSS	Fetal Adrenal Gland	Adrenal Gland
45	chr7:100209200-100210400	Active TSS	Fetal Intestine Large	intestine
46	chr7:100209200-100210400	Active TSS	Fetal Intestine Small	intestine
47	chr7:100209200-100210400	Active TSS	Rectal Mucosa Donor 31	rectum
48	chr7:100209200-100210400	Active TSS	Skeletal Muscle Female	skeletal muscle
49	chr7:100209200-100210400	Active TSS	Thymus	Thymus
50	chr7:100209200-100210400	Active TSS	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links