Variant report

Variant	rs73156210
Chromosome Location	chr7:100182468-100182469
allele	G/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	MXI1	chr7:100182097-100184976	IMR90	lung:	n/a	n/a
2	REST	chr7:100182398-100182962	K562	blood:	n/a	chr7:100182669-100182678
3	ZEB1	chr7:100182146-100184048	GM12878	blood:	n/a	chr7:100183211-100183218 chr7:100183232-100183243 chr7:100183231-100183243 chr7:100182601-100182608 chr7:100182599-100182611 chr7:100182600-100182611
4	POLR2A	chr7:100182296-100182769	H1-hESC	embryonic stem cell:	n/a	n/a
5	TBL1XR1	chr7:100182450-100182497	GM12878	blood:	n/a	n/a
6	ATF2	chr7:100182363-100183005	H1-hESC	embryonic stem cell:	n/a	n/a
7	ZEB1	chr7:100182352-100183736	HepG2	liver:	n/a	chr7:100183211-100183218 chr7:100183232-100183243 chr7:100183231-100183243 chr7:100182601-100182608 chr7:100182599-100182611 chr7:100182600-100182611
8	TEAD4	chr7:100182312-100182718	H1-hESC	embryonic stem cell:	n/a	n/a
9	CREB1	chr7:100182306-100184537	H1-hESC	embryonic stem cell:	n/a	n/a
10	RCOR1	chr7:100182400-100183256	Hela-S3	cervix:	n/a	n/a
11	MAX	chr7:100182149-100182487	K562	blood:	n/a	n/a
12	POLR2A	chr7:100182266-100182753	H1-hESC	embryonic stem cell:	n/a	n/a
13	ZNF263	chr7:100182277-100182994	HEK293-T-REx	kidney:	n/a	chr7:100182523-100182532 chr7:100182522-100182543
14	MXI1	chr7:100182428-100182525	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr7:100182222-100182501	HepG2	liver:	n/a	n/a
16	NR2F2	chr7:100181959-100184907	K562	blood:	n/a	n/a
17	POLR2A	chr7:100182288-100183047	K562	blood:	n/a	n/a
18	CREB1	chr7:100182352-100183443	H1-hESC	embryonic stem cell:	n/a	n/a
19	TBL1XR1	chr7:100182460-100182956	K562	blood:	n/a	n/a
20	ZEB1	chr7:100182398-100184620	HepG2	liver:	n/a	chr7:100183211-100183218 chr7:100183232-100183243 chr7:100183231-100183243 chr7:100182601-100182608 chr7:100182599-100182611 chr7:100182600-100182611
21	POLR2A	chr7:100182174-100184954	K562	blood:	n/a	n/a
22	MAZ	chr7:100180708-100184962	IMR90	lung:	n/a	chr7:100181374-100181384 chr7:100184537-100184547 chr7:100182041-100182051
23	SP1	chr7:100182185-100184559	H1-hESC	embryonic stem cell:	n/a	chr7:100183001-100183010 chr7:100182542-100182551 chr7:100183411-100183422 chr7:100183001-100183011 chr7:100183000-100183012 chr7:100183874-100183895 chr7:100183766-100183780 chr7:100183776-100183786 chr7:100183216-100183228 chr7:100183777-100183786 chr7:100182997-100183011 chr7:100183776-100183790 chr7:100182646-100182659 chr7:100182621-100182631 chr7:100184533-100184542 chr7:100183001-100183011 chr7:100182621-100182635 chr7:100184536-100184548 chr7:100183000-100183012 chr7:100183002-100183011 chr7:100183213-100183227 chr7:100182622-100182631 chr7:100183216-100183228 chr7:100183770-100183784 chr7:100183218-100183227 chr7:100183002-100183011
24	RCOR1	chr7:100182281-100182481	GM12878	blood:	n/a	n/a
25	NR2F2	chr7:100182128-100184517	MCF-7	breast:	n/a	n/a
26	TEAD4	chr7:100182261-100182661	H1-hESC	embryonic stem cell:	n/a	n/a
27	RFX5	chr7:100182322-100185183	SK-N-SH	brain:	n/a	chr7:100183876-100183885
28	NR2F2	chr7:100182251-100183670	MCF-7	breast:	n/a	n/a
29	USF2	chr7:100182438-100182610	H1-hESC	embryonic stem cell:	n/a	chr7:100182543-100182559
30	MAX	chr7:100182329-100184949	MCF-7	breast:	n/a	chr7:100184537-100184547
31	SIN3AK20	chr7:100182118-100184807	MCF-7	breast:	n/a	n/a
32	POLR2A	chr7:100182056-100182783	GM12878	blood:	n/a	n/a
33	POLR2A	chr7:100182003-100185028	H1-hESC	embryonic stem cell:	n/a	n/a
34	TEAD4	chr7:100182381-100183051	K562	blood:	n/a	n/a
35	ZNF143	chr7:100182410-100182485	H1-hESC	embryonic stem cell:	n/a	n/a
36	SP1	chr7:100182380-100184684	HCT-116	colon:	n/a	chr7:100183001-100183010 chr7:100182542-100182551 chr7:100183411-100183422 chr7:100183001-100183011 chr7:100183000-100183012 chr7:100183874-100183895 chr7:100183766-100183780 chr7:100183776-100183786 chr7:100183216-100183228 chr7:100183777-100183786 chr7:100182997-100183011 chr7:100183776-100183790 chr7:100182646-100182659 chr7:100182621-100182631 chr7:100184533-100184542 chr7:100183001-100183011 chr7:100182621-100182635 chr7:100184536-100184548 chr7:100183000-100183012 chr7:100183002-100183011 chr7:100183213-100183227 chr7:100182622-100182631 chr7:100183216-100183228 chr7:100183770-100183784 chr7:100183218-100183227 chr7:100183002-100183011
37	TBP	chr7:100182346-100182504	H1-hESC	embryonic stem cell:	n/a	n/a
38	SP1	chr7:100182407-100182813	H1-hESC	embryonic stem cell:	n/a	chr7:100182542-100182551 chr7:100182646-100182659 chr7:100182621-100182631 chr7:100182621-100182635 chr7:100182622-100182631
39	SPI1	chr7:100180976-100182585	HL-60	blood:	n/a	chr7:100181849-100181858 chr7:100181545-100181558 chr7:100182173-100182186 chr7:100181845-100181854 chr7:100181847-100181860 chr7:100181310-100181317 chr7:100181848-100181861 chr7:100181848-100181861 chr7:100182178-100182191 chr7:100181316-100181329
40	SIN3A	chr7:100182276-100184927	H1-hESC	embryonic stem cell:	n/a	chr7:100183989-100184002
41	SIN3AK20	chr7:100182114-100182752	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr7:100182354-100182731	MCF-7	breast:	n/a	n/a
43	SMARCC1	chr7:100182287-100184840	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:100182236..100184425-chr7:100238898..100241261,2	MCF-7	breast:
2	chr5:109124372..109125150-chr7:100181922..100182732,2	Hela-S3	cervix:
3	chr11:65264056..65266842-chr7:100182390..100184760,2	MCF-7	breast:
4	chr7:100080695..100082892-chr7:100181914..100185450,4	MCF-7	breast:
5	chr7:100181910..100186072-chr7:100207984..100213440,10	MCF-7	breast:
6	chr7:100182175..100185247-chr7:100208524..100211802,7	K562	blood:
7	chr7:100080109..100082832-chr7:100180830..100183809,4	MCF-7	breast:
8	chr7:100180263..100184567-chr7:100269497..100273047,5	K562	blood:
9	chr7:100179326..100185857-chr7:100269460..100275597,19	MCF-7	breast:
10	chr7:100180934..100186212-chr7:100208003..100211666,10	K562	blood:
11	chr7:100182086..100185168-chr7:100253147..100256450,3	MCF-7	breast:
12	chr7:100031924..100034212-chr7:100179842..100183716,3	MCF-7	breast:
13	chr7:100180512..100183004-chr7:100452297..100454557,2	MCF-7	breast:
14	chr7:100181058..100187386-chr7:100198846..100203499,12	K562	blood:
15	chr7:100075021..100078361-chr7:100180649..100185937,5	MCF-7	breast:
16	chr7:100182178..100184822-chr7:100229744..100231921,2	K562	blood:
17	chr7:100070743..100075629-chr7:100178965..100183270,7	K562	blood:
18	chr7:100181696..100183356-chr7:100285003..100287484,2	K562	blood:
19	chr7:100181873..100185085-chr7:100229346..100230888,3	MCF-7	breast:
20	chr7:100178369..100186125-chr7:100269651..100278553,26	MCF-7	breast:
21	chr7:100181018..100185569-chr7:100200264..100204023,6	MCF-7	breast:
22	chr7:100031790..100034595-chr7:100181557..100184454,2	MCF-7	breast:
23	chr7:100024456..100030636-chr7:100180698..100187996,13	K562	blood:
24	chr7:100075632..100078427-chr7:100182362..100185442,6	K562	blood:
25	chr7:100181244..100182815-chr7:100224206..100225875,2	MCF-7	breast:
26	chr7:100182229..100186397-chr7:100301308..100304608,4	MCF-7	breast:
27	chr7:100182211..100184849-chr7:100486903..100489190,3	MCF-7	breast:
28	chr7:100181605..100184428-chr7:100302112..100307493,7	MCF-7	breast:
29	chr7:100026775..100029248-chr7:100181334..100183939,2	MCF-7	breast:
30	chr7:100065519..100069193-chr7:100181232..100183900,3	MCF-7	breast:
31	chr7:100024988..100028445-chr7:100180808..100186978,10	K562	blood:
32	chr7:100024997..100029018-chr7:100182448..100185836,5	MCF-7	breast:
33	chr7:100181574..100184448-chr7:100269546..100273047,4	K562	blood:
34	chr7:100181643..100184250-chr7:100471958..100474283,2	MCF-7	breast:
35	chr7:100075509..100078207-chr7:100182258..100185575,5	K562	blood:

Variant related genes	Relation type
FBXO24	TF binding region
LRCH4	TF binding region
ENSG00000266372	Chromatin interaction
ENSG00000106327	Chromatin interaction
ENSG00000146828	Chromatin interaction
ENSG00000166924	Chromatin interaction
ENSG00000106330	Chromatin interaction
ENSG00000146830	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000241357	Chromatin interaction
ENSG00000224729	Chromatin interaction
ENSG00000270117	Chromatin interaction
ENSG00000106333	Chromatin interaction
ENSG00000077080	Chromatin interaction
ENSG00000176125	Chromatin interaction
ENSG00000172354	Chromatin interaction
ENSG00000172336	Chromatin interaction
ENSG00000240211	Chromatin interaction
ENSG00000087087	Chromatin interaction
ENSG00000166925	Chromatin interaction
ENSG00000160813	Chromatin interaction
ENSG00000251562	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11972116	0.94[EUR][1000 genomes]
rs11977607	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11978096	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11978967	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12154919	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12216707	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2406243	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34440977	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56307653	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58509206	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60668677	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60743967	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61309832	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61318457	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67147615	0.90[EUR][1000 genomes]
rs67535650	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6970240	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73154884	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73154887	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73154891	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73154894	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73154895	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73154897	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73154902	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73156207	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73156208	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73156211	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73711133	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73711136	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73711137	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7784759	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7799695	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 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	nsv888776	chr7:100014711-100198386	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	297 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	nsv888780	chr7:100032665-100198386	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
7	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
8	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
9	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
10	nsv888788	chr7:100161557-100186066	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	52 gene(s)	inside rSNPs	diseases
11	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
12	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
13	nsv607932	chr7:100172495-100182691	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs73156210	SAP25	cis	Artery Tibial	GTEx
rs73156210	SAP25	cis	Thyroid	GTEx
rs73156210	SAP25	cis	Esophagus Muscularis	GTEx
rs73156210	LRCH4	cis	Esophagus Muscularis	GTEx
rs73156210	SAP25	cis	Nerve Tibial	GTEx

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100180000-100182600	Weak transcription	Aorta	Aorta
2	chr7:100180000-100182600	Enhancers	Fetal Heart	heart
3	chr7:100180000-100182600	Weak transcription	Ovary	ovary
4	chr7:100180000-100182800	Enhancers	Placenta Amnion	Placenta Amnion
5	chr7:100180000-100183400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:100180200-100183000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr7:100180200-100183400	Flanking Active TSS	Primary hematopoietic stem cells	blood
8	chr7:100180400-100182800	Flanking Active TSS	Fetal Intestine Large	intestine
9	chr7:100180400-100183200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr7:100180400-100183400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
11	chr7:100180400-100183400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
12	chr7:100180600-100182800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr7:100180600-100183200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:100180600-100183400	Flanking Active TSS	Primary B cells from cord blood	blood
15	chr7:100180600-100183400	Flanking Active TSS	Primary B cells from peripheral blood	blood
16	chr7:100180600-100183400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
17	chr7:100180600-100183800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
18	chr7:100180800-100182600	Transcr. at gene 5' and 3'	NHLF	lung
19	chr7:100180800-100183000	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
20	chr7:100180800-100183400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr7:100180800-100183400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
22	chr7:100181000-100183000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
23	chr7:100181000-100183200	Flanking Active TSS	Dnd41	blood
24	chr7:100181000-100183400	Flanking Active TSS	Fetal Thymus	thymus
25	chr7:100181000-100183600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
26	chr7:100181200-100182600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr7:100181200-100182600	Active TSS	Primary T helper naive cells from peripheral blood	blood
28	chr7:100181200-100182600	Transcr. at gene 5' and 3'	Esophagus	oesophagus
29	chr7:100181200-100182800	Transcr. at gene 5' and 3'	Thymus	Thymus
30	chr7:100181200-100184600	Active TSS	Primary T cells from cord blood	blood
31	chr7:100181200-100185000	Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr7:100181400-100182600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr7:100181400-100183400	Flanking Active TSS	Fetal Muscle Leg	muscle
34	chr7:100181600-100183000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:100181600-100183200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
36	chr7:100181600-100184800	Active TSS	Small Intestine	intestine
37	chr7:100181800-100183600	Active TSS	Right Atrium	heart
38	chr7:100181800-100184800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
39	chr7:100181800-100184800	Active TSS	Lung	lung
40	chr7:100181800-100185000	Active TSS	H9 Cell Line	embryonic stem cell
41	chr7:100181800-100185000	Active TSS	iPS-18 Cell Line	embryonic stem cell
42	chr7:100181800-100185000	Active TSS	Pancreatic Islets	Pancreatic Islet
43	chr7:100182000-100182600	Enhancers	Spleen	Spleen
44	chr7:100182000-100183200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr7:100182000-100183200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr7:100182000-100184600	Active TSS	HSMM	muscle
47	chr7:100182000-100184800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr7:100182200-100182600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
49	chr7:100182200-100182800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
50	chr7:100182200-100182800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links