Variant report

Variant	rs2959654
Chromosome Location	chr11:64412086-64412087
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9)
CpG islands
(count:122)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:64411167-64429413	U87	brain:	n/a	n/a
2	POLR2A	chr11:64411167-64414430	U87	brain:	n/a	n/a
3	POLR2A	chr11:64411429-64412144	U87	brain:	n/a	n/a
4	POLR2A	chr11:64409300-64412311	H1-neurons	neurons:	n/a	n/a
5	CTBP2	chr11:64411785-64412217	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr11:64411960-64412110	NHEK	skin:	n/a	n/a
7	POLR2A	chr11:64411378-64412144	U87	brain:	n/a	n/a
8	POLR2A	chr11:64412020-64412167	H1-hESC	embryonic stem cell:	n/a	n/a
9	SIN3A	chr11:64411872-64412599	H1-hESC	embryonic stem cell:	n/a	chr11:64412399-64412413 chr11:64412383-64412392

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:64412079-64412129	PANC-1	pancreas:	n/a
2	chr11:64412085-64412135	SK-N-SH	brain:	n/a
3	chr11:64412085-64412135	NB4	blood:	n/a
4	chr11:64412085-64412135	K562	blood:	n/a
5	chr11:64412079-64412129	GM12892	blood:	n/a
6	chr11:64412085-64412135	CMK	blood:	n/a
7	chr11:64412079-64412129	Jurkat	blood:	n/a
8	chr11:64412079-64412129	GM06990	blood:	n/a
9	chr11:64412079-64412129	HIPEpiC	eye:	n/a
10	chr11:64412085-64412135	ovcar-3	ovarian:	n/a
11	chr11:64412079-64412129	HMEC	breast:	n/a
12	chr11:64412079-64412129	ECC-1	luminal epithelium:	n/a
13	chr11:64412079-64412129	Caco-2	colon:	n/a
14	chr11:64412079-64412129	GM12891	blood:	n/a
15	chr11:64412085-64412135	AG10803	skin:	n/a
16	chr11:64412085-64412135	HCT-116	colon:	n/a
17	chr11:64412079-64412129	HL-60	blood:	n/a
18	chr11:64412085-64412135	SK-N-MC	brain:	n/a
19	chr11:64412079-64412129	SKMC	muscle:	n/a
20	chr11:64412085-64412135	GM12892	blood:	n/a
21	chr11:64412079-64412129	HEK293	kidney:	embryo
22	chr11:64412085-64412135	BJ	skin:	n/a
23	chr11:64412085-64412135	Caco-2	colon:	n/a
24	chr11:64412079-64412129	ovcar-3	ovarian:	n/a
25	chr11:64412079-64412129	AG09319	gingival:	n/a
26	chr11:64412079-64412129	H1-hESC	embryonic stem cell:	embryo
27	chr11:64412085-64412135	HEK293	kidney:	embryo
28	chr11:64412085-64412135	HPAEpiC	pulmonary alveolar:	n/a
29	chr11:64412085-64412135	HMEC	breast:	n/a
30	chr11:64412079-64412129	HUVEC	blood vessel:	n/a
31	chr11:64412079-64412129	HRPEpiC	eye:	n/a
32	chr11:64412079-64412129	AG09309	skin:	n/a
33	chr11:64412085-64412135	HNPCEpiC	eye:	n/a
34	chr11:64412085-64412135	U87	brain:	n/a
35	chr11:64412085-64412135	HCPEpiC	choroid plexus:	n/a
36	chr11:64412085-64412135	T-47D	breast:	n/a
37	chr11:64412079-64412129	BJ	skin:	n/a
38	chr11:64412085-64412135	SKMC	muscle:	n/a
39	chr11:64412085-64412135	HepG2	liver:	n/a
40	chr11:64412085-64412135	HRCEpiC	kidney:	n/a
41	chr11:64412085-64412135	GM19239	blood:	n/a
42	chr11:64412085-64412135	HRPEpiC	eye:	n/a
43	chr11:64412079-64412129	AG04450	lung:	fetal
44	chr11:64412079-64412129	LNCaP	prostate:	n/a
45	chr11:64412079-64412129	Hela-S3	cervix:	n/a
46	chr11:64412085-64412135	SK-N-SH_RA	brain:	n/a
47	chr11:64412079-64412129	SK-N-SH	brain:	n/a
48	chr11:64412085-64412135	NHBE	bronchial:	n/a
49	chr11:64412085-64412135	AG04450	lung:	fetal
50	chr11:64412085-64412135	PANC-1	pancreas:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:64411217..64413501-chr11:64452044..64454513,2	K562	blood:
2	chr11:64411039..64413414-chr11:64416751..64419165,4	K562	blood:
3	11:64187725-64189071..11:64402707-64415880	K562	blood:
4	chr11:64320459..64321631-chr11:64411779..64413112,6	MCF-7	breast:

No data

Variant related genes	Relation type
NRXN2	TF binding region
ENSG00000237410	TF binding region
NRXN2	CpG island
ENSG00000237410	CpG island
ENSG00000231492	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10128590	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10792445	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10897519	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10897521	0.94[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231837	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231838	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231848	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11605121	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1207179	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1207226	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1212146	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12269736	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17146216	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2022051	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2269730	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2285339	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2361216	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2957564	0.81[AMR][1000 genomes]
rs471618	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs490192	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs502567	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs506035	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs516117	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs530252	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs530775	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs557709	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55908793	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56105921	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61884406	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7117423	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7121121	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7128467	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72927012	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7929296	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7929627	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7932775	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7937990	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs948689	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897693	chr11:64305452-64440920	Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv2422214	chr11:64312491-64483418	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv832188	chr11:64315368-64485209	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv468596	chr11:64334114-64527080	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv555195	chr11:64334114-64527080	Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv897694	chr11:64334114-64584959	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
7	nsv818842	chr11:64345448-64546391	Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
8	nsv528506	chr11:64345448-64701030	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
9	nsv555196	chr11:64357072-64559898	Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
10	nsv897695	chr11:64357072-64701030	Weak transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
11	nsv897696	chr11:64365796-64412877	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv1051350	chr11:64372906-64533632	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
13	nsv555198	chr11:64373899-64573589	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
14	esv1804443	chr11:64386453-64534785	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
15	esv3330626	chr11:64409926-64412124	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2959654	NRXN2	cis	lung	GTEx

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64410600-64412200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr11:64411200-64412400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
3	chr11:64411400-64412200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
4	chr11:64411400-64412200	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:64411400-64412200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
6	chr11:64411400-64412200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
7	chr11:64411400-64412200	Bivalent Enhancer	Fetal Heart	heart
8	chr11:64411400-64412400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
9	chr11:64411400-64412400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
10	chr11:64411400-64412400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
11	chr11:64411400-64412800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
12	chr11:64411400-64413000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr11:64411400-64413000	Bivalent Enhancer	Fetal Thymus	thymus
14	chr11:64411400-64413200	Bivalent Enhancer	NHDF-Ad	bronchial
15	chr11:64411400-64413400	Bivalent Enhancer	Fetal Intestine Large	intestine
16	chr11:64411400-64413600	Bivalent Enhancer	Fetal Intestine Small	intestine
17	chr11:64411600-64412200	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
18	chr11:64411600-64412200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr11:64411600-64412200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
20	chr11:64411600-64412200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr11:64411600-64412200	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr11:64411600-64412200	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
23	chr11:64411600-64412200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
24	chr11:64411600-64412400	Strong transcription	Right Atrium	heart
25	chr11:64411600-64412600	Weak transcription	Pancreas	Pancrea
26	chr11:64411600-64412600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
27	chr11:64411600-64412800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr11:64411600-64412800	Bivalent Enhancer	Fetal Stomach	stomach
29	chr11:64411600-64413200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr11:64411600-64427800	Weak transcription	Aorta	Aorta
31	chr11:64411800-64412200	Bivalent Enhancer	Fetal Kidney	kidney
32	chr11:64411800-64412400	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr11:64411800-64412400	Bivalent Enhancer	Fetal Lung	lung
34	chr11:64411800-64412600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr11:64411800-64412600	Enhancers	Brain Hippocampus Middle	brain
36	chr11:64411800-64412800	Enhancers	Primary hematopoietic stem cells	blood
37	chr11:64411800-64412800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr11:64411800-64412800	Enhancers	Fetal Brain Male	brain
39	chr11:64411800-64413000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr11:64411800-64413800	Bivalent Enhancer	Fetal Muscle Leg	muscle
41	chr11:64411800-64414200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr11:64411800-64416800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr11:64411800-64420000	Weak transcription	Brain Substantia Nigra	brain
44	chr11:64411800-64420200	Weak transcription	Brain Cingulate Gyrus	brain
45	chr11:64411800-64420400	Weak transcription	Brain Angular Gyrus	brain
46	chr11:64412000-64412200	Flanking Bivalent TSS/Enh	H9 Cell Line	embryonic stem cell
47	chr11:64412000-64412200	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
48	chr11:64412000-64412200	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr11:64412000-64412200	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:64412000-64412200	Enhancers	Primary B cells from cord blood	blood

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