Variant report

Variant	rs61891586
Chromosome Location	chr11:67139870-67139871
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	ZBTB7A	chr11:67139504-67140234	ECC-1	luminal epithelium:	n/a	n/a
2	POLR2A	chr11:67138563-67140098	HL-60	blood:	n/a	n/a
3	ZBTB7A	chr11:67139523-67139979	K562	blood:	n/a	n/a
4	SIN3AK20	chr11:67139835-67142256	MCF-7	breast:	n/a	n/a
5	SP1	chr11:67138681-67140293	A549	lung:	n/a	chr11:67139670-67139684 chr11:67139762-67139776 chr11:67139211-67139221
6	SIN3AK20	chr11:67139644-67140072	PANC-1	pancreas:	n/a	n/a
7	BCL3	chr11:67138621-67140141	A549	lung:	n/a	chr11:67139091-67139104
8	POLR2A	chr11:67134317-67140357	U87	brain:	n/a	n/a
9	HEY1	chr11:67139832-67140017	K562	blood:	n/a	n/a
10	EP300	chr11:67138695-67140234	A549	lung:	n/a	chr11:67140185-67140201
11	POLR2A	chr11:67139835-67142244	K562	blood:	n/a	n/a
12	TAF1	chr11:67138969-67141226	A549	lung:	n/a	n/a
13	POLR2A	chr11:67138593-67142764	PANC-1	pancreas:	n/a	n/a
14	REST	chr11:67138541-67140080	A549	lung:	n/a	n/a
15	TCF12	chr11:67137930-67144339	A549	lung:	n/a	chr11:67138193-67138203 chr11:67139958-67139965 chr11:67139242-67139249 chr11:67141661-67141671 chr11:67144056-67144066 chr11:67138192-67138199 chr11:67142524-67142532 chr11:67139957-67139967 chr11:67142516-67142526 chr11:67139956-67139963
16	POLR2A	chr11:67138898-67140078	A549	lung:	n/a	n/a
17	POLR2A	chr11:67138915-67142701	MCF-7	breast:	n/a	n/a
18	HA-E2F1	chr11:67139849-67140982	Hela-S3	cervix:	n/a	chr11:67140264-67140275 chr11:67140158-67140165 chr11:67140336-67140346 chr11:67140266-67140274 chr11:67140791-67140801 chr11:67140158-67140165 chr11:67140266-67140274 chr11:67140265-67140275 chr11:67140267-67140274 chr11:67140158-67140165
19	MAX	chr11:67139804-67140004	K562	blood:	n/a	n/a
20	HMGN3	chr11:67139719-67139919	K562	blood:	n/a	n/a
21	CREB1	chr11:67139769-67140555	A549	lung:	n/a	n/a
22	SP1	chr11:67138783-67140235	A549	lung:	n/a	chr11:67139670-67139684 chr11:67139762-67139776 chr11:67139211-67139221
23	POLR2A	chr11:67139773-67139912	ProgFib	skin:	n/a	n/a
24	MXI1	chr11:67136428-67142794	IMR90	lung:	n/a	n/a
25	MAX	chr11:67139387-67141420	K562	blood:	n/a	chr11:67141256-67141266 chr11:67141367-67141377
26	POLR2A	chr11:67137865-67142671	K562	blood:	n/a	n/a
27	E2F6	chr11:67139696-67141023	K562	blood:	n/a	chr11:67140264-67140275 chr11:67140158-67140165 chr11:67140336-67140346 chr11:67140266-67140274 chr11:67140791-67140801 chr11:67140158-67140165 chr11:67140266-67140274 chr11:67140600-67140611 chr11:67140265-67140275 chr11:67140267-67140274 chr11:67140158-67140165
28	CTCF	chr11:67138358-67139875	A549	lung:	n/a	chr11:67139137-67139150
29	POLR2A	chr11:67139833-67141142	A549	lung:	n/a	n/a
30	POLR2A	chr11:67139559-67139886	SK-N-SH	brain:	n/a	n/a
31	MAZ	chr11:67138879-67142345	K562	blood:	n/a	chr11:67141256-67141266 chr11:67141367-67141377 chr11:67139214-67139223
32	POLR2A	chr11:67139762-67142124	HUVEC	blood vessel:	n/a	n/a
33	POLR2A	chr11:67138754-67139881	U87	brain:	n/a	n/a
34	PBX3	chr11:67138788-67140664	A549	lung:	n/a	n/a
35	REST	chr11:67139758-67140030	A549	lung:	n/a	n/a
36	ZBTB7A	chr11:67139611-67142343	K562	blood:	n/a	n/a
37	EGR1	chr11:67139863-67140365	K562	blood:	n/a	chr11:67140045-67140059
38	ZBTB7A	chr11:67138888-67140220	ECC-1	luminal epithelium:	n/a	n/a
39	POLR2A	chr11:67135652-67140351	U87	brain:	n/a	n/a
40	POLR2A	chr11:67138770-67141183	A549	lung:	n/a	n/a
41	MAX	chr11:67137318-67145655	A549	lung:	n/a	chr11:67138167-67138177 chr11:67141256-67141266 chr11:67138019-67138029 chr11:67141367-67141377 chr11:67139214-67139223
42	JUND	chr11:67138885-67143692	A549	lung:	n/a	chr11:67141685-67141694 chr11:67141991-67142001 chr11:67141990-67142002 chr11:67141990-67142001 chr11:67141992-67142000 chr11:67141993-67142004 chr11:67142329-67142340 chr11:67141991-67142001 chr11:67140956-67140965 chr11:67142827-67142836 chr11:67141991-67142001
43	MAX	chr11:67138561-67140292	A549	lung:	n/a	chr11:67139214-67139223
44	POLR2A	chr11:67138788-67140062	PANC-1	pancreas:	n/a	n/a
45	POLR2A	chr11:67137182-67142767	K562	blood:	n/a	n/a
46	POLR2A	chr11:67139658-67139884	K562	blood:	n/a	n/a
47	PBX3	chr11:67139105-67140403	A549	lung:	n/a	n/a
48	MAX	chr11:67139842-67139977	A549	lung:	n/a	n/a
49	POLR2A	chr11:67139785-67140050	HCT-116	colon:	n/a	n/a
50	TBL1XR1	chr11:67139860-67139924	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67085099..67087143-chr11:67137966..67139875,2	K562	blood:
2	chr11:67138591..67140616-chr11:67149692..67150721,9	MCF-7	breast:
3	chr11:66821897..66826528-chr11:67139094..67144065,11	MCF-7	breast:
4	chr11:67138235..67140028-chr11:67271265..67273106,2	MCF-7	breast:
5	chr11:67031846..67035344-chr11:67139453..67142374,3	K562	blood:
6	chr11:66622570..66624423-chr11:67139168..67140990,2	MCF-7	breast:
7	chr11:67006828..67010582-chr11:67138867..67142453,4	MCF-7	breast:
8	chr11:67053474..67057507-chr11:67138689..67143945,8	MCF-7	breast:
9	chr11:67138872..67142169-chr11:67249496..67254071,4	MCF-7	breast:
10	chr11:66788543..66790931-chr11:67139607..67141552,2	MCF-7	breast:
11	chr11:66823034..66824892-chr11:67139520..67142366,3	MCF-7	breast:
12	chr11:66845534..66847277-chr11:67139384..67140950,2	MCF-7	breast:
13	chr11:67139479..67140053-chr11:67149261..67150255,2	K562	blood:
14	chr11:67139765..67142051-chr17:57918264..57920706,2	MCF-7	breast:
15	chr11:67137032..67142528-chr11:67234580..67238729,6	MCF-7	breast:
16	chr11:67138903..67140672-chr11:67189332..67192243,2	K562	blood:
17	chr11:67006855..67009254-chr11:67139637..67141684,2	MCF-7	breast:
18	chr11:67138865..67141337-chr11:67205315..67206965,2	K562	blood:
19	chr11:62608228..62609142-chr11:67139785..67140767,2	HCT-116	colon:
20	chr11:67138430..67143112-chr11:67157518..67161987,7	K562	blood:
21	chr11:67139501..67142119-chr16:3071898..3074181,2	MCF-7	breast:
22	chr11:67070466..67072644-chr11:67139702..67142015,2	K562	blood:
23	chr11:67088208..67091047-chr11:67138396..67140194,2	MCF-7	breast:
24	chr11:67139623..67143035-chr11:67167894..67169679,3	K562	blood:
25	chr11:67069839..67071996-chr11:67139740..67141397,2	MCF-7	breast:
26	chr11:67138420..67140492-chr11:67271610..67274474,2	K562	blood:
27	chr11:67138426..67140382-chr11:67217472..67219205,2	K562	blood:
28	chr11:67069246..67073295-chr11:67139634..67145393,8	MCF-7	breast:
29	chr11:67044106..67046398-chr11:67138784..67140765,2	K562	blood:
30	chr11:67078342..67081725-chr11:67139517..67143464,5	MCF-7	breast:
31	chr11:66886882..66888512-chr11:67137835..67140678,2	MCF-7	breast:
32	chr11:67030856..67037366-chr11:67138319..67144892,13	MCF-7	breast:
33	chr11:67116951..67127260-chr11:67135118..67146037,42	K562	blood:
34	chr11:67139414..67143301-chr11:67273275..67276817,6	MCF-7	breast:

Variant related genes	Relation type
CLCF1	TF binding region
ENSG00000103145	Chromatin interaction
ENSG00000110711	Chromatin interaction
ENSG00000167797	Chromatin interaction
ENSG00000173120	Chromatin interaction
ENSG00000173020	Chromatin interaction
ENSG00000172830	Chromatin interaction
ENSG00000131652	Chromatin interaction
ENSG00000173227	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000173156	Chromatin interaction
ENSG00000175482	Chromatin interaction
ENSG00000110697	Chromatin interaction
ENSG00000172531	Chromatin interaction
ENSG00000172613	Chromatin interaction
ENSG00000173621	Chromatin interaction
ENSG00000172932	Chromatin interaction
ENSG00000172663	Chromatin interaction
ENSG00000213402	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10896165	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11227740	0.83[ASN][1000 genomes]
rs11227742	0.83[ASN][1000 genomes]
rs11227744	0.83[ASN][1000 genomes]
rs11227745	0.83[ASN][1000 genomes]
rs11227746	0.83[ASN][1000 genomes]
rs11227750	0.88[ASN][1000 genomes]
rs11227751	0.83[ASN][1000 genomes]
rs11227752	0.88[ASN][1000 genomes]
rs11227761	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11227765	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11227768	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11227770	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11227786	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11227787	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12223898	0.88[ASN][1000 genomes]
rs12274774	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17879849	1.00[AMR][1000 genomes]
rs3730145	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56132056	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs58100805	0.83[ASN][1000 genomes]
rs61758508	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61889551	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61889552	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61891588	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61891589	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61891590	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs61891592	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7127431	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9630209	0.88[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	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic 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	271 gene(s)	inside rSNPs	diseases
2	nsv933183	chr11:67008447-67160993	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv897796	chr11:67021518-67186000	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
4	nsv897797	chr11:67023040-67293234	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	206 gene(s)	inside rSNPs	diseases
5	nsv1043037	chr11:67027193-67357425	Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
6	nsv468603	chr11:67033076-67164495	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
7	nsv555253	chr11:67033076-67164495	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised 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 target site	85 gene(s)	inside rSNPs	diseases
8	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers 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	236 gene(s)	inside rSNPs	diseases
9	nsv1047890	chr11:67058231-67184436	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
10	nsv1048230	chr11:67058231-67252397	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
11	nsv897804	chr11:67090571-67224278	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
12	nsv1039205	chr11:67135246-67252397	Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
13	esv1818769	chr11:67138811-67300457	Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	167 gene(s)	inside rSNPs	diseases
14	esv3404685	chr11:67139076-67142024	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	38 gene(s)	inside rSNPs	diseases
15	esv3326147	chr11:67139201-67141749	Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	38 gene(s)	inside rSNPs	diseases
16	esv3323213	chr11:67139601-67142149	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	38 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67136600-67140000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr11:67136800-67143600	Bivalent Enhancer	Fetal Thymus	thymus
3	chr11:67137000-67140000	Flanking Active TSS	Stomach Smooth Muscle	stomach
4	chr11:67137600-67140200	Bivalent Enhancer	Dnd41	blood
5	chr11:67138000-67140000	Flanking Active TSS	NH-A	brain
6	chr11:67138200-67140000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr11:67138200-67140000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr11:67138400-67140000	Flanking Active TSS	Hela-S3	cervix
9	chr11:67138800-67140000	Flanking Active TSS	Primary B cells from cord blood	blood
10	chr11:67138800-67140000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
11	chr11:67138800-67140000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
12	chr11:67139000-67140000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
13	chr11:67139000-67140000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
14	chr11:67139000-67140000	Flanking Active TSS	Primary B cells from peripheral blood	blood
15	chr11:67139000-67140000	Flanking Active TSS	Colonic Mucosa	Colon
16	chr11:67139000-67140000	Flanking Active TSS	Pancreas	Pancrea
17	chr11:67139000-67140000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
18	chr11:67139000-67140200	Enhancers	Brain Cingulate Gyrus	brain
19	chr11:67139000-67141600	Active TSS	HSMMtube	muscle
20	chr11:67139200-67140000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr11:67139200-67140000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:67139200-67140000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr11:67139200-67140000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
24	chr11:67139200-67140000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
25	chr11:67139200-67140000	Flanking Active TSS	Brain Anterior Caudate	brain
26	chr11:67139200-67140000	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
27	chr11:67139200-67140000	Flanking Active TSS	Duodenum Mucosa	Duodenum
28	chr11:67139200-67140000	Flanking Active TSS	Fetal Intestine Large	intestine
29	chr11:67139200-67140000	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
30	chr11:67139200-67140000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
31	chr11:67139200-67140000	Flanking Active TSS	HepG2	liver
32	chr11:67139200-67140000	Flanking Active TSS	K562	blood
33	chr11:67139200-67141600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
34	chr11:67139400-67140000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr11:67139400-67140000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
36	chr11:67139400-67140000	Flanking Active TSS	Primary hematopoietic stem cells	blood
37	chr11:67139400-67140000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
38	chr11:67139400-67140000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
39	chr11:67139400-67140000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
40	chr11:67139400-67140000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr11:67139400-67140000	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr11:67139400-67140000	Flanking Active TSS	Right Ventricle	heart
43	chr11:67139400-67141000	Transcr. at gene 5' and 3'	Right Atrium	heart
44	chr11:67139400-67141600	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr11:67139400-67141800	Active TSS	Fetal Kidney	kidney
46	chr11:67139400-67142000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr11:67139400-67142000	Active TSS	Muscle Satellite Cultured Cells	--
48	chr11:67139600-67140000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
49	chr11:67139600-67140000	Enhancers	Primary T cells from cord blood	blood
50	chr11:67139600-67140000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain

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