Variant report

Variant	rs12223627
Chromosome Location	chr11:62368557-62368558
allele	C/G
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	HEY1	chr11:62368534-62369558	HepG2	liver:	n/a	chr11:62369092-62369107
2	POLR2A	chr11:62367896-62369805	PFSK-1	brain:	n/a	n/a
3	POLR2A	chr11:62368434-62369831	GM12892	blood:	n/a	n/a
4	POLR2A	chr11:62368442-62369554	MCF-7	breast:	n/a	n/a
5	MAX	chr11:62368345-62369697	HepG2	liver:	n/a	n/a
6	POLR2A	chr11:62368267-62370415	K562	blood:	n/a	n/a
7	CREB1	chr11:62368548-62369296	A549	lung:	n/a	n/a
8	TAF1	chr11:62368510-62369534	PFSK-1	brain:	n/a	n/a
9	BCL3	chr11:62368532-62369687	A549	lung:	n/a	chr11:62368925-62368938 chr11:62368931-62368940 chr11:62369058-62369067 chr11:62369212-62369221 chr11:62369660-62369673
10	YY1	chr11:62368424-62369734	K562	blood:	n/a	chr11:62368674-62368688 chr11:62369039-62369053 chr11:62368932-62368941 chr11:62369213-62369222 chr11:62368571-62368582 chr11:62369091-62369105 chr11:62369042-62369056 chr11:62368933-62368947
11	EP300	chr11:62368441-62370351	ECC-1	luminal epithelium:	n/a	chr11:62369378-62369385 chr11:62368934-62368950
12	UBTF	chr11:62368112-62369993	K562	blood:	n/a	n/a
13	POLR2A	chr11:62368494-62369950	SK-N-SH	brain:	n/a	n/a
14	YY1	chr11:62368398-62369323	GM12891	blood:	n/a	chr11:62368674-62368688 chr11:62369039-62369053 chr11:62368932-62368941 chr11:62369213-62369222 chr11:62368571-62368582 chr11:62369091-62369105 chr11:62369042-62369056 chr11:62368933-62368947
15	POLR2A	chr11:62368536-62369802	ProgFib	skin:	n/a	n/a
16	ELF1	chr11:62368461-62369847	GM12878	blood:	n/a	chr11:62369376-62369389 chr11:62368934-62368946 chr11:62369212-62369224 chr11:62368938-62368947 chr11:62369650-62369659 chr11:62368932-62368941 chr11:62369660-62369669 chr11:62368526-62368537
17	POLR2A	chr11:62368444-62369960	GM19193	blood:	n/a	n/a
18	POLR2A	chr11:62367492-62370094	SK-N-MC	brain:	n/a	n/a
19	CHD2	chr11:62368532-62369732	GM12878	blood:	n/a	chr11:62369509-62369519 chr11:62368807-62368817 chr11:62368545-62368555
20	POLR2A	chr11:62368509-62369875	GM19099	blood:	n/a	n/a
21	POLR2A	chr11:62368488-62369904	GM18951	blood:	n/a	n/a
22	POLR2A	chr11:62368295-62370454	GM12878	blood:	n/a	n/a
23	POLR2A	chr11:62368445-62369802	H1-neurons	neurons:	n/a	n/a
24	TAF1	chr11:62368530-62369942	H1-neurons	neurons:	n/a	n/a
25	MAX	chr11:62368399-62370429	K562	blood:	n/a	n/a
26	ELF1	chr11:62368524-62369682	MCF-7	breast:	n/a	chr11:62369376-62369389 chr11:62368934-62368946 chr11:62369212-62369224 chr11:62368938-62368947 chr11:62369650-62369659 chr11:62368932-62368941 chr11:62369660-62369669 chr11:62368526-62368537
27	GABPA	chr11:62368438-62369027	A549	lung:	n/a	n/a
28	ZNF143	chr11:62368522-62369663	GM12878	blood:	n/a	chr11:62368972-62368982 chr11:62368634-62368652 chr11:62369640-62369658 chr11:62368877-62368887
29	RUNX3	chr11:62367997-62369816	GM12878	blood:	n/a	n/a
30	SIN3AK20	chr11:62367777-62369689	MCF-7	breast:	n/a	n/a
31	TAF1	chr11:62368543-62369573	HepG2	liver:	n/a	n/a
32	YY1	chr11:62368415-62369408	GM12892	blood:	n/a	chr11:62368674-62368688 chr11:62369039-62369053 chr11:62368932-62368941 chr11:62369213-62369222 chr11:62368571-62368582 chr11:62369091-62369105 chr11:62369042-62369056 chr11:62368933-62368947
33	SMC3	chr11:62368345-62368869	Hela-S3	cervix:	n/a	chr11:62368813-62368827
34	POLR2A	chr11:62368352-62370040	U87	brain:	n/a	n/a
35	HCFC1	chr11:62367839-62371522	Hela-S3	cervix:	n/a	n/a
36	SIN3AK20	chr11:62368440-62369208	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr11:62368323-62370634	K562	blood:	n/a	n/a
38	GABPA	chr11:62368550-62368967	K562	blood:	n/a	n/a
39	POLR2A	chr11:62367904-62369869	GM12878	blood:	n/a	n/a
40	SIN3AK20	chr11:62368401-62369526	PANC-1	pancreas:	n/a	n/a
41	NFIC	chr11:62368529-62369101	GM12878	blood:	n/a	n/a
42	CHD1	chr11:62365894-62370422	IMR90	lung:	n/a	chr11:62369509-62369519 chr11:62368807-62368817 chr11:62368545-62368555
43	GABPA	chr11:62368410-62369687	MCF-7	breast:	n/a	chr11:62369213-62369222 chr11:62369087-62369096
44	GABPA	chr11:62368404-62369582	SK-N-SH	brain:	n/a	chr11:62369213-62369222 chr11:62369087-62369096
45	POLR2A	chr11:62368369-62370399	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr11:62368511-62369857	GM12878	blood:	n/a	n/a
47	HMGN3	chr11:62368449-62370875	K562	blood:	n/a	n/a
48	MAZ	chr11:62367943-62370617	IMR90	lung:	n/a	n/a
49	TCF12	chr11:62368263-62370026	A549	lung:	n/a	chr11:62368342-62368349
50	PAX5	chr11:62368535-62369004	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:62368512..62370789-chr11:62571314..62573375,3	K562	blood:
2	chr11:62367818..62370152-chr11:64017422..64019610,2	MCF-7	breast:
3	chr11:62367343..62369766-chr11:62446126..62447935,2	MCF-7	breast:
4	chr11:62368131..62371520-chr11:62438403..62441108,5	K562	blood:
5	chr11:62367786..62371340-chr11:62553206..62555734,4	K562	blood:
6	chr11:62366402..62370002-chr11:62419166..62421218,5	MCF-7	breast:
7	chr11:62365951..62369565-chr11:62622521..62625872,5	K562	blood:
8	chr11:62366839..62369029-chr11:62472927..62475049,2	MCF-7	breast:
9	chr11:62366079..62370074-chr11:62386678..62390504,7	MCF-7	breast:
10	chr11:62340363..62343212-chr11:62365252..62369475,4	MCF-7	breast:
11	chr11:62362631..62371847-chr11:62427548..62442313,26	MCF-7	breast:
12	chr11:62367185..62372634-chr11:62607154..62610784,6	MCF-7	breast:
13	chr11:62365870..62369296-chr11:62605447..62609594,6	K562	blood:
14	chr11:62366145..62371000-chr11:62493302..62496531,6	K562	blood:
15	chr11:62366894..62368811-chr11:62572540..62574175,2	MCF-7	breast:
16	chr11:62365873..62371127-chr11:62605447..62611263,11	K562	blood:
17	chr11:62367890..62370349-chr11:62493262..62495403,4	K562	blood:
18	chr11:62361223..62372590-chr11:62430599..62435389,30	K562	blood:
19	chr11:62359044..62359737-chr11:62368478..62369085,2	MCF-7	breast:
20	chr11:62366089..62368766-chr11:62475317..62477241,2	MCF-7	breast:
21	chr11:62365667..62370630-chr11:62493549..62497299,5	MCF-7	breast:
22	chr11:62355264..62375429-chr11:62428418..62443271,77	MCF-7	breast:
23	chr11:62368326..62369108-chr11:62379751..62380601,2	MCF-7	breast:
24	chr11:62367943..62370017-chr11:62571875..62574574,2	K562	blood:
25	chr11:62365983..62370724-chr11:62412063..62418373,9	K562	blood:
26	chr11:62366955..62369844-chr11:62535933..62538904,2	K562	blood:
27	chr11:62367573..62370441-chr11:62435647..62437526,2	K562	blood:
28	chr11:62368550..62369244-chr17:74099398..74100291,2	NB4	blood:
29	chr11:62365338..62373022-chr11:62621930..62625872,13	K562	blood:
30	chr11:62367640..62370552-chr11:62646699..62650475,4	K562	blood:
31	chr11:62363464..62373052-chr11:62429645..62434985,23	K562	blood:
32	chr11:62344267..62349689-chr11:62366431..62369887,5	MCF-7	breast:
33	chr11:62365089..62370067-chr11:62436026..62441323,7	K562	blood:
34	chr11:62366910..62368974-chr11:62608295..62610836,2	MCF-7	breast:
35	chr11:62367785..62371189-chr11:62419322..62422312,3	K562	blood:
36	chr11:62366689..62370631-chr11:62475430..62478411,3	MCF-7	breast:
37	chr11:62367022..62370613-chr11:62412660..62415093,5	MCF-7	breast:
38	chr11:62368041..62369560-chr11:62472282..62474702,2	K562	blood:
39	chr11:62367086..62370916-chr11:62552894..62556677,4	MCF-7	breast:

Variant related genes	Relation type
MTA2	TF binding region
ENSG00000149489	Chromatin interaction
ENSG00000149782	Chromatin interaction
ENSG00000162194	Chromatin interaction
ENSG00000149499	Chromatin interaction
ENSG00000254772	Chromatin interaction
ENSG00000206597	Chromatin interaction
ENSG00000089597	Chromatin interaction
ENSG00000162227	Chromatin interaction
ENSG00000185475	Chromatin interaction
ENSG00000214756	Chromatin interaction
ENSG00000149541	Chromatin interaction
ENSG00000255432	Chromatin interaction
ENSG00000168000	Chromatin interaction
ENSG00000214753	Chromatin interaction
ENSG00000255717	Chromatin interaction
ENSG00000168003	Chromatin interaction
ENSG00000162191	Chromatin interaction
ENSG00000182473	Chromatin interaction
ENSG00000204922	Chromatin interaction
ENSG00000162231	Chromatin interaction
ENSG00000269176	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000185085	Chromatin interaction
ENSG00000149016	Chromatin interaction
ENSG00000255508	Chromatin interaction
ENSG00000234857	Chromatin interaction
ENSG00000162222	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1061093	0.80[ASN][1000 genomes]
rs11231137	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11231138	0.80[AFR][1000 genomes]
rs11231141	0.80[ASN][1000 genomes]
rs11231144	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs11231145	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs11231150	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs11231151	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11231152	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs11231154	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231155	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11231156	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231161	0.81[ASN][1000 genomes]
rs12049914	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12225213	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12226821	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1801144	0.86[ASN][1000 genomes]
rs2516633	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2516634	0.88[ASN][1000 genomes]
rs2849030	0.88[ASN][1000 genomes]
rs2849031	0.88[ASN][1000 genomes]
rs34065644	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34894392	0.88[ASN][1000 genomes]
rs35587183	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs35880596	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs3923805	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60098285	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61296092	0.80[ASN][1000 genomes]
rs67308910	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7124057	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs71490390	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs71490392	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs71490394	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72927213	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72927237	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7928833	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7930896	0.82[AFR][1000 genomes]
rs7942154	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7942991	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7943191	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915636	chr11:62016992-62713565	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1441 gene(s)	inside rSNPs	diseases
2	nsv532283	chr11:62201358-62863475	Enhancers Flanking Active TSS Genic enhancers Strong transcription Weak transcription Active TSS 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 miRNA target site	1433 gene(s)	inside rSNPs	diseases
3	nsv532284	chr11:62220043-62630253	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription 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	1401 gene(s)	inside rSNPs	diseases
4	esv3584599	chr11:62262742-62398050	Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS 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	156 gene(s)	inside rSNPs	diseases
5	nsv832182	chr11:62295575-62462848	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
6	nsv825939	chr11:62326083-62410577	Flanking Active TSS Genic enhancers Strong transcription Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
7	nsv497903	chr11:62330308-62608042	Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	489 gene(s)	inside rSNPs	diseases
8	nsv555174	chr11:62334096-62496519	Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription 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	243 gene(s)	inside rSNPs	diseases
9	nsv897622	chr11:62366986-62392229	Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs12223627	EML3	cis	Whole Blood	GTEx
rs12223627	EML3	cis	Esophagus Mucosa	GTEx
rs12223627	EEF1G	cis	multi-tissue	Pritchard
rs12223627	MTA2	cis	Esophagus Mucosa	GTEx

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:62366400-62368800	Flanking Active TSS	Primary B cells from cord blood	blood
2	chr11:62367000-62368600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr11:62367000-62369200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
4	chr11:62367200-62368600	Flanking Active TSS	Adipose Nuclei	Adipose
5	chr11:62367200-62368600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
6	chr11:62367200-62368600	Flanking Active TSS	Stomach Smooth Muscle	stomach
7	chr11:62367200-62369200	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
8	chr11:62367400-62368600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr11:62367400-62368600	Flanking Active TSS	Liver	Liver
10	chr11:62367400-62369600	Active TSS	HMEC	breast
11	chr11:62367400-62369600	Active TSS	NHEK	skin
12	chr11:62367600-62368600	Flanking Active TSS	Placenta	Placenta
13	chr11:62367600-62370000	Active TSS	Right Atrium	heart
14	chr11:62367600-62370400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr11:62367600-62370600	Active TSS	Ovary	ovary
16	chr11:62367600-62370800	Active TSS	Aorta	Aorta
17	chr11:62367800-62368600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
18	chr11:62367800-62369400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr11:62367800-62369400	Active TSS	NH-A	brain
20	chr11:62367800-62369600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr11:62367800-62369600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr11:62367800-62369600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr11:62367800-62369600	Active TSS	Muscle Satellite Cultured Cells	--
24	chr11:62367800-62369600	Active TSS	Lung	lung
25	chr11:62367800-62369600	Active TSS	Thymus	Thymus
26	chr11:62367800-62370000	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr11:62367800-62370000	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr11:62367800-62370200	Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr11:62367800-62370200	Active TSS	Breast Myoepithelial Primary Cells	Breast
30	chr11:62367800-62370200	Active TSS	Fetal Kidney	kidney
31	chr11:62367800-62370600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr11:62367800-62370600	Active TSS	Psoas Muscle	Psoas
33	chr11:62368000-62368600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
34	chr11:62368000-62368600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr11:62368000-62369400	Active TSS	Primary T killer memory cells from peripheral blood	blood
36	chr11:62368000-62369600	Active TSS	Primary T helper naive cells from peripheral blood	blood
37	chr11:62368000-62369600	Active TSS	Primary T helper cells PMA-I stimulated	--
38	chr11:62368000-62369600	Active TSS	GM12878-XiMat	blood
39	chr11:62368000-62369600	Active TSS	NHLF	lung
40	chr11:62368000-62370000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr11:62368000-62370000	Active TSS	Gastric	stomach
42	chr11:62368000-62370000	Active TSS	Placenta Amnion	Placenta Amnion
43	chr11:62368000-62370200	Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr11:62368200-62368600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
45	chr11:62368200-62368600	Flanking Active TSS	Primary B cells from peripheral blood	blood
46	chr11:62368200-62368600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr11:62368200-62368600	Flanking Active TSS	Fetal Muscle Trunk	muscle
48	chr11:62368200-62368800	Bivalent/Poised TSS	HepG2	liver
49	chr11:62368200-62369400	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
50	chr11:62368200-62369600	Active TSS	H1 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links