Variant report

Variant	rs2010404
Chromosome Location	chr11:67777082-67777083
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:111)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:111 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr11:67776841-67779086	A549	lung:	n/a	n/a
2	RAD21	chr11:67777037-67778612	Hela-S3	cervix:	n/a	n/a
3	MAX	chr11:67777077-67778668	Hela-S3	cervix:	n/a	n/a
4	CUX1	chr11:67776941-67777606	K562	blood:	n/a	n/a
5	IRF1	chr11:67776909-67777273	K562	blood:	n/a	n/a
6	STAT5A	chr11:67776826-67777370	K562	blood:	n/a	n/a
7	RAD21	chr11:67777072-67777367	K562	blood:	n/a	n/a
8	TBL1XR1	chr11:67776919-67777349	K562	blood:	n/a	n/a
9	POLR2A	chr11:67777053-67778982	HL-60	blood:	n/a	n/a
10	GATA1	chr11:67776599-67777966	PBDE	blood:	n/a	n/a
11	CTCF	chr11:67777040-67777190	A549	lung:	n/a	n/a
12	EP300	chr11:67776703-67779274	A549	lung:	n/a	n/a
13	KAP1	chr11:67776722-67777238	HEK293	kidney:	n/a	n/a
14	RAD21	chr11:67776998-67778000	HepG2	liver:	n/a	n/a
15	MAFF	chr11:67777008-67777284	K562	blood:	n/a	n/a
16	RAD21	chr11:67777043-67777361	GM12878	blood:	n/a	n/a
17	GATA2	chr11:67776880-67777397	K562	blood:	n/a	n/a
18	MYC	chr11:67776921-67777129	K562	blood:	n/a	n/a
19	CTCF	chr11:67777056-67777412	K562	blood:	n/a	n/a
20	NR3C1	chr11:67776798-67777309	A549	lung:	n/a	n/a
21	CEBPD	chr11:67776963-67777374	K562	blood:	n/a	n/a
22	ZBTB7A	chr11:67776869-67777099	K562	blood:	n/a	n/a
23	POLR2A	chr11:67777032-67778102	K562	blood:	n/a	n/a
24	RAD21	chr11:67777016-67777396	SK-N-SH_RA	brain:	n/a	n/a
25	ZNF143	chr11:67776864-67777232	K562	blood:	n/a	n/a
26	CTCF	chr11:67776932-67777340	A549	lung:	n/a	n/a
27	SP1	chr11:67776718-67782739	A549	lung:	n/a	chr11:67782714-67782728 chr11:67782346-67782355 chr11:67782347-67782356 chr11:67782346-67782360
28	RAD21	chr11:67777065-67777422	A549	lung:	n/a	n/a
29	RAD21	chr11:67777064-67777382	A549	lung:	n/a	n/a
30	BRCA1	chr11:67777072-67778731	Hela-S3	cervix:	n/a	n/a
31	SIN3AK20	chr11:67777016-67777397	A549	lung:	n/a	n/a
32	MYC	chr11:67776940-67777254	K562	blood:	n/a	n/a
33	ATF1	chr11:67777013-67777242	K562	blood:	n/a	n/a
34	CTCF	chr11:67777043-67777398	A549	lung:	n/a	n/a
35	ZNF384	chr11:67777031-67777406	GM12878	blood:	n/a	n/a
36	RCOR1	chr11:67777066-67778568	Hela-S3	cervix:	n/a	n/a
37	TEAD4	chr11:67776846-67777360	K562	blood:	n/a	n/a
38	REST	chr11:67776947-67782855	A549	lung:	n/a	chr11:67782466-67782475 chr11:67782075-67782089 chr11:67782425-67782438 chr11:67782093-67782106 chr11:67782268-67782277
39	CTCF	chr11:67777028-67777411	GM12878	blood:	n/a	n/a
40	SIX5	chr11:67776699-67783266	A549	lung:	n/a	n/a
41	CTCF	chr11:67776946-67777970	HCT-116	colon:	n/a	n/a
42	TAL1	chr11:67776795-67777713	K562	blood:	n/a	n/a
43	RAD21	chr11:67777045-67777405	GM12878	blood:	n/a	n/a
44	USF1	chr11:67776789-67777242	K562	blood:	n/a	n/a
45	NR2F2	chr11:67776640-67777894	K562	blood:	n/a	n/a
46	TEAD4	chr11:67776583-67777869	K562	blood:	n/a	n/a
47	ARID3A	chr11:67776891-67777356	K562	blood:	n/a	n/a
48	CTCF	chr11:67776872-67778088	SK-N-SH	brain:	n/a	n/a
49	CTCF	chr11:67777080-67777230	HAc	cerebellar:	n/a	n/a
50	MAZ	chr11:67776692-67778793	IMR90	lung:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67776209..67777895-chr11:67887404..67889163,2	K562	blood:
2	chr11:65270883..65271821-chr11:67776699..67777645,2	Hela-S3	cervix:
3	chr11:67776633..67779501-chr11:67798153..67800329,2	K562	blood:
4	chr11:67776362..67777982-chr11:67979637..67981259,2	K562	blood:
5	chr11:67776892..67777625-chr11:67788855..67789447,2	MCF-7	breast:
6	chr11:67776804..67777352-chr11:67788052..67788668,2	MCF-7	breast:
7	chr11:67770463..67774040-chr11:67774088..67778740,6	K562	blood:
8	chr11:67770966..67773282-chr11:67774269..67777181,2	K562	blood:
9	chr11:67776791..67777547-chr11:67788251..67788807,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC93B1-1	chr11:67776909-67782033	NONHSAT022487

No data

Variant related genes	Relation type
ALDH3B1	TF binding region
UNC93B1	TF binding region
ENSG00000006534	Chromatin interaction
ENSG00000110066	Chromatin interaction
ENSG00000110057	Chromatin interaction
ENSG00000110721	Chromatin interaction
ENSG00000110717	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12418774	1.00[YRI][hapmap]
rs2286170	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3763941	0.85[ASN][1000 genomes]
rs3764818	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3794176	0.89[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.91[ASN][1000 genomes]
rs475325	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs55759735	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:36 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036101	chr11:67346813-67828351	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
2	nsv541079	chr11:67346813-67828351	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
3	nsv468606	chr11:67352689-67816936	Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
4	nsv555269	chr11:67352689-67816936	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS 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	136 gene(s)	inside rSNPs	diseases
5	nsv427892	chr11:67451649-67926562	Bivalent Enhancer Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
6	esv2757450	chr11:67472905-67891289	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
7	esv2759835	chr11:67472905-67891289	Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
8	nsv428260	chr11:67524937-67797669	Enhancers Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
9	esv2758275	chr11:67524937-67859490	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	87 gene(s)	inside rSNPs	diseases
10	nsv469856	chr11:67639037-67859490	Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
11	nsv482760	chr11:67639037-67859490	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
12	nsv1038960	chr11:67727827-67785555	Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
13	nsv1047567	chr11:67747160-67819790	Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
14	nsv8836	chr11:67752879-67819799	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
15	nsv983037	chr11:67756642-67778389	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
16	nsv897836	chr11:67757350-67816936	Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
17	nsv897837	chr11:67757350-67821036	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
18	nsv897838	chr11:67757350-67833543	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
19	nsv825963	chr11:67763676-68197054	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
20	nsv1050471	chr11:67764068-67821610	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
21	nsv897839	chr11:67765056-67793014	Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
22	nsv468613	chr11:67765056-67794643	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
23	nsv555277	chr11:67765056-67794643	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
24	nsv468614	chr11:67765056-67799926	ZNF genes & repeats Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
25	nsv897840	chr11:67765056-67804605	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
26	nsv468615	chr11:67765056-67816936	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
27	nsv555278	chr11:67765056-67816936	Enhancers Genic enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
28	nsv897841	chr11:67765056-67816936	Bivalent Enhancer Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
29	nsv469964	chr11:67765056-67821036	Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
30	nsv897842	chr11:67765056-67821036	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
31	nsv897843	chr11:67765056-67833543	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
32	nsv1046054	chr11:67768796-67819790	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	60 gene(s)	inside rSNPs	diseases
33	nsv897844	chr11:67772729-67793014	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
34	nsv897845	chr11:67774231-67821036	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
35	nsv897846	chr11:67776465-67794643	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription 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	49 gene(s)	inside rSNPs	diseases
36	nsv897847	chr11:67776465-67804605	Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67771600-67777200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr11:67771600-67797600	Weak transcription	Small Intestine	intestine
3	chr11:67772000-67777200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr11:67772200-67777200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr11:67772200-67777200	Weak transcription	Left Ventricle	heart
6	chr11:67772200-67777400	Weak transcription	NHLF	lung
7	chr11:67772200-67777800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr11:67772200-67779200	Enhancers	Primary B cells from peripheral blood	blood
9	chr11:67772400-67777400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr11:67772600-67777400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr11:67772600-67792400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr11:67772800-67777200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr11:67772800-67777200	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr11:67772800-67777200	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr11:67772800-67777800	Weak transcription	Lung	lung
16	chr11:67773600-67777800	Enhancers	Stomach Mucosa	stomach
17	chr11:67775000-67777600	Enhancers	Fetal Muscle Leg	muscle
18	chr11:67775000-67782400	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr11:67775200-67777200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr11:67775200-67777400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr11:67775200-67777400	Enhancers	Placenta	Placenta
22	chr11:67775200-67777600	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr11:67775200-67777800	Enhancers	Pancreas	Pancrea
24	chr11:67775400-67777400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr11:67775400-67777400	Enhancers	Fetal Intestine Large	intestine
26	chr11:67775400-67777400	Enhancers	Fetal Intestine Small	intestine
27	chr11:67775400-67777600	Enhancers	Adipose Nuclei	Adipose
28	chr11:67775400-67778200	Enhancers	Primary hematopoietic stem cells	blood
29	chr11:67775400-67778200	Enhancers	Spleen	Spleen
30	chr11:67775600-67777400	Flanking Active TSS	Hela-S3	cervix
31	chr11:67775600-67777600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr11:67775600-67779400	Enhancers	Fetal Heart	heart
33	chr11:67775800-67777400	Flanking Active TSS	HepG2	liver
34	chr11:67775800-67777400	Enhancers	HMEC	breast
35	chr11:67775800-67777400	Enhancers	HSMMtube	muscle
36	chr11:67775800-67777600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr11:67775800-67777600	Enhancers	Brain Anterior Caudate	brain
38	chr11:67775800-67777600	Enhancers	Brain Hippocampus Middle	brain
39	chr11:67775800-67777600	Enhancers	Brain Substantia Nigra	brain
40	chr11:67775800-67777600	Enhancers	Esophagus	oesophagus
41	chr11:67775800-67777800	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr11:67775800-67777800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr11:67775800-67777800	Enhancers	Liver	Liver
44	chr11:67775800-67777800	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr11:67775800-67777800	Enhancers	Thymus	Thymus
46	chr11:67776000-67777400	Enhancers	Muscle Satellite Cultured Cells	--
47	chr11:67776000-67777400	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr11:67776000-67777600	Enhancers	Primary B cells from cord blood	blood
49	chr11:67776000-67777600	Enhancers	Fetal Muscle Trunk	muscle
50	chr11:67776000-67777600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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