Variant report

Variant	rs13305995
Chromosome Location	chr1:153651589-153651590
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:43)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:43 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAX	chr1:153651027-153652501	HepG2	liver:	n/a	n/a
2	CTCF	chr1:153649966-153652441	SK-N-SH	brain:	n/a	chr1:153650334-153650350 chr1:153650333-153650351 chr1:153650335-153650356
3	SIN3A	chr1:153650093-153653005	H1-hESC	embryonic stem cell:	n/a	chr1:153650997-153651008 chr1:153651070-153651081
4	CTBP2	chr1:153650221-153652352	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr1:153650737-153651985	Hela-S3	cervix:	n/a	n/a
6	MAZ	chr1:153650187-153651936	Hela-S3	cervix:	n/a	chr1:153650950-153650959
7	ZBTB7A	chr1:153650079-153651822	ECC-1	luminal epithelium:	n/a	chr1:153651151-153651158 chr1:153651397-153651404
8	RFX5	chr1:153651006-153651769	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr1:153651520-153651670	SAEC	small airway:	n/a	n/a
10	SMARCC1	chr1:153650257-153651631	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr1:153651560-153651710	GM12878	blood:	n/a	n/a
12	MAX	chr1:153650753-153651934	ECC-1	luminal epithelium:	n/a	chr1:153650950-153650959
13	CTCF	chr1:153651560-153651710	GM12865	blood:	n/a	n/a
14	MYC	chr1:153651490-153651925	MCF-7	breast:	n/a	n/a
15	SMC3	chr1:153650051-153651758	Hela-S3	cervix:	n/a	chr1:153650335-153650349
16	MAX	chr1:153650983-153652510	H1-hESC	embryonic stem cell:	n/a	n/a
17	RCOR1	chr1:153650148-153651662	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr1:153650891-153651885	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr1:153651540-153651690	NHEK	skin:	n/a	n/a
20	ZBTB7A	chr1:153650093-153651789	ECC-1	luminal epithelium:	n/a	chr1:153651151-153651158 chr1:153651397-153651404
21	MAX	chr1:153650835-153651874	ECC-1	luminal epithelium:	n/a	chr1:153650950-153650959
22	BACH1	chr1:153650174-153652415	H1-hESC	embryonic stem cell:	n/a	n/a
23	SUZ12	chr1:153650317-153653157	NT2-D1	testis:	n/a	n/a
24	NRF1	chr1:153651519-153651665	GM12878	blood:	n/a	n/a
25	MAX	chr1:153650157-153651819	A549	lung:	n/a	chr1:153650950-153650959
26	CTCF	chr1:153651583-153651633	Lung_OC	lung:	n/a	n/a
27	ZNF263	chr1:153650185-153652312	HEK293-T-REx	kidney:	n/a	chr1:153651268-153651289 chr1:153650506-153650515 chr1:153651010-153651019 chr1:153651225-153651246
28	MAX	chr1:153650916-153651871	MCF-7	breast:	n/a	chr1:153650950-153650959
29	TCF12	chr1:153650922-153651980	ECC-1	luminal epithelium:	n/a	chr1:153651358-153651368
30	SMARCB1	chr1:153650705-153652434	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr1:153651520-153651670	GM12865	blood:	n/a	n/a
32	SMC3	chr1:153649978-153652192	SK-N-SH	brain:	n/a	chr1:153650335-153650349
33	POLR2A	chr1:153650962-153652061	MCF-7	breast:	n/a	n/a
34	CTCF	chr1:153651440-153651590	AG04449	skin:	n/a	n/a
35	CTCF	chr1:153651500-153651650	HVMF	connective:	n/a	n/a
36	E2F6	chr1:153650861-153651787	A549	lung:	n/a	chr1:153651004-153651013 chr1:153651379-153651388 chr1:153651220-153651234
37	CTCF	chr1:153651500-153651650	GM12866	blood:	n/a	n/a
38	MXI1	chr1:153650189-153651887	Hela-S3	cervix:	n/a	n/a
39	MAX	chr1:153650189-153651920	Hela-S3	cervix:	n/a	chr1:153650950-153650959
40	MAX	chr1:153651138-153652266	GM12878	blood:	n/a	n/a
41	MAX	chr1:153650095-153652049	A549	lung:	n/a	chr1:153650950-153650959
42	TCF12	chr1:153651231-153651840	A549	lung:	n/a	chr1:153651358-153651368
43	POLR2A	chr1:153650965-153651813	H1-neurons	neurons:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:153651568-153651618	ECC-1	luminal epithelium:	n/a
2	chr1:153651568-153651618	H1-hESC	embryonic stem cell:	embryo
3	chr1:153651568-153651618	AG04449	skin:	fetal
4	chr1:153651568-153651618	HRPEpiC	eye:	n/a
5	chr1:153651568-153651618	HCT-116	colon:	n/a
6	chr1:153651568-153651618	AoSMC	blood vessel:	n/a
7	chr1:153651568-153651618	AG04450	lung:	fetal
8	chr1:153651568-153651618	NHBE	bronchial:	n/a
9	chr1:153651568-153651618	NT2-D1	testis:	n/a
10	chr1:153651568-153651618	HEK293	kidney:	embryo
11	chr1:153651568-153651618	BE2_C	brain:	n/a
12	chr1:153651568-153651618	GM06990	blood:	n/a
13	chr1:153651568-153651618	PFSK-1	brain:	n/a
14	chr1:153651568-153651618	ProgFib	skin:	n/a
15	chr1:153651568-153651618	RPTEC	kidney:	n/a
16	chr1:153651568-153651618	ovcar-3	ovarian:	n/a
17	chr1:153651568-153651618	GM12892	blood:	n/a
18	chr1:153651568-153651618	HRE	kidney:	n/a
19	chr1:153651568-153651618	AG10803	skin:	n/a
20	chr1:153651568-153651618	PrEC	prostate:	n/a
21	chr1:153651568-153651618	SK-N-SH	brain:	n/a
22	chr1:153651568-153651618	Hepatocyte	liver:	n/a
23	chr1:153651568-153651618	HUVEC	blood vessel:	n/a
24	chr1:153651568-153651618	LNCaP	prostate:	n/a
25	chr1:153651568-153651618	Caco-2	colon:	n/a
26	chr1:153651568-153651618	IMR90	lung:	fetal
27	chr1:153651568-153651618	SKMC	muscle:	n/a
28	chr1:153651568-153651618	HCPEpiC	choroid plexus:	n/a
29	chr1:153651568-153651618	MCF10A-Er-Src	breast:	n/a
30	chr1:153651568-153651618	SAEC	small airway:	n/a
31	chr1:153651568-153651618	HEEpiC	esophagus:	n/a
32	chr1:153651568-153651618	Hela-S3	cervix:	n/a
33	chr1:153651568-153651618	GM12878	blood:	n/a
34	chr1:153651568-153651618	T-47D	breast:	n/a
35	chr1:153651568-153651618	AG09309	skin:	n/a
36	chr1:153651568-153651618	NHDF-neo	bronchial:	n/a
37	chr1:153651568-153651618	Jurkat	blood:	n/a
38	chr1:153651568-153651618	HMEC	breast:	n/a
39	chr1:153651568-153651618	AG09319	gingival:	n/a
40	chr1:153651568-153651618	CMK	blood:	n/a
41	chr1:153651568-153651618	HNPCEpiC	eye:	n/a
42	chr1:153651568-153651618	PANC-1	pancreas:	n/a
43	chr1:153651568-153651618	GM19239	blood:	n/a
44	chr1:153651568-153651618	HCM	heart:	n/a
45	chr1:153651568-153651618	HepG2	liver:	n/a
46	chr1:153651568-153651618	HRCEpiC	kidney:	n/a
47	chr1:153651568-153651618	GM12891	blood:	n/a
48	chr1:153651568-153651618	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:153651568-153651618	NH-A	brain:	n/a
50	chr1:153651568-153651618	HL-60	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:153651109..153660855-chr1:153698392..153702896,14	MCF-7	breast:
2	chr1:153650787..153653048-chr1:153700479..153702624,2	K562	blood:
3	chr1:153648500..153651688-chr1:153746725..153749419,3	MCF-7	breast:
4	chr1:153651404..153652981-chr1:153702351..153704100,2	MCF-7	breast:
5	chr1:153641478..153645789-chr1:153651108..153654010,4	K562	blood:
6	chr1:153651116..153652910-chr1:153740976..153746594,4	MCF-7	breast:
7	chr1:153640859..153647825-chr1:153650423..153657512,10	K562	blood:
8	chr1:153651029..153654025-chr1:153963195..153965197,2	MCF-7	breast:

No data

Variant related genes	Relation type
NPR1	TF binding region
NPR1	CpG island
ENSG00000143621	Chromatin interaction
ENSG00000199565	Chromatin interaction
ENSG00000143624	Chromatin interaction
ENSG00000143554	Chromatin interaction
ENSG00000177954	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10082235	0.86[ASN][1000 genomes]
rs11264279	0.86[ASN][1000 genomes]
rs11805092	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11808118	1.00[ASN][1000 genomes]
rs12097725	0.86[ASN][1000 genomes]
rs13305996	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13305998	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13306004	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28437915	0.86[ASN][1000 genomes]
rs34192791	1.00[ASN][1000 genomes]
rs57304273	1.00[ASN][1000 genomes]
rs59770064	0.86[ASN][1000 genomes]
rs61806716	0.86[ASN][1000 genomes]
rs6665831	0.86[ASN][1000 genomes]
rs6688800	0.85[AMR][1000 genomes]
rs6692298	0.86[ASN][1000 genomes]
rs73011738	0.86[ASN][1000 genomes]
rs73011760	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7516222	0.86[ASN][1000 genomes]
rs7518794	0.86[ASN][1000 genomes]
rs7520299	0.86[ASN][1000 genomes]
rs7536700	0.86[ASN][1000 genomes]
rs7547783	0.86[ASN][1000 genomes]
rs7547790	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010488	chr1:152901263-153670972	Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
2	nsv535171	chr1:152901263-153670972	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
3	nsv547928	chr1:153612133-153714252	Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	esv2830411	chr1:153613393-153725007	Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
5	nsv1067771	chr1:153613593-153724866	Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Enhancers 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 miRNA target site	48 gene(s)	inside rSNPs	diseases
6	nsv530052	chr1:153613593-153724866	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
7	nsv1005818	chr1:153613597-153724980	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription 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	48 gene(s)	inside rSNPs	diseases
8	nsv535173	chr1:153613597-153724980	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' 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	48 gene(s)	inside rSNPs	diseases
9	nsv1007835	chr1:153613597-153729959	Genic enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Active 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 miRNA target site	48 gene(s)	inside rSNPs	diseases
10	nsv535174	chr1:153613597-153729959	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS 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 miRNA target site	48 gene(s)	inside rSNPs	diseases
11	nsv1011897	chr1:153613597-153836703	Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking 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	70 gene(s)	inside rSNPs	diseases
12	nsv464028	chr1:153622220-153723037	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
13	nsv547929	chr1:153622220-153723037	Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
14	nsv999364	chr1:153622634-154419436	Strong transcription Genic enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' 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	286 gene(s)	inside rSNPs	diseases
15	nsv535175	chr1:153622634-154419436	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	286 gene(s)	inside rSNPs	diseases
16	nsv1001312	chr1:153622834-153724867	Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
17	nsv535176	chr1:153622834-153724867	Active TSS Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153650000-153652400	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
2	chr1:153650000-153653200	Active TSS	Fetal Kidney	kidney
3	chr1:153650200-153652400	Flanking Active TSS	Adipose Nuclei	Adipose
4	chr1:153650200-153652400	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
5	chr1:153650200-153652600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:153650200-153652800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
7	chr1:153650400-153651600	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:153650400-153652000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
9	chr1:153650400-153652400	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
10	chr1:153650400-153652400	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
11	chr1:153650400-153652400	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
12	chr1:153650400-153652400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
13	chr1:153650400-153652400	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
14	chr1:153650400-153652400	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
15	chr1:153650400-153652600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr1:153650400-153652600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
17	chr1:153650400-153653000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:153650400-153653200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
19	chr1:153650400-153653400	Active TSS	Aorta	Aorta
20	chr1:153650600-153651600	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
21	chr1:153650600-153651600	Flanking Bivalent TSS/Enh	NHEK	skin
22	chr1:153650600-153651600	Flanking Bivalent TSS/Enh	Osteobl	bone
23	chr1:153650600-153652000	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr1:153650600-153652000	Flanking Active TSS	Pancreas	Pancrea
25	chr1:153650600-153652000	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 31	rectum
26	chr1:153650600-153652200	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr1:153650600-153652400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:153650600-153652400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr1:153650600-153652400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:153650600-153652400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr1:153650600-153652400	Flanking Active TSS	Right Ventricle	heart
32	chr1:153650600-153652400	Flanking Bivalent TSS/Enh	GM12878-XiMat	blood
33	chr1:153650600-153652400	Flanking Bivalent TSS/Enh	HepG2	liver
34	chr1:153650600-153652400	Flanking Bivalent TSS/Enh	NHLF	lung
35	chr1:153650600-153652600	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr1:153650600-153652600	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr1:153650600-153652600	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
38	chr1:153650600-153652600	Flanking Bivalent TSS/Enh	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr1:153650600-153652600	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
40	chr1:153650600-153652600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr1:153650600-153652800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
42	chr1:153650600-153652800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
43	chr1:153650600-153653200	Active TSS	Left Ventricle	heart
44	chr1:153650600-153653400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr1:153650800-153651600	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
46	chr1:153650800-153651600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
47	chr1:153650800-153651600	Active TSS	A549	lung
48	chr1:153650800-153651800	Active TSS	Hela-S3	cervix
49	chr1:153650800-153651800	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
50	chr1:153650800-153652000	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood

The 2.0 version of rSNPBase

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