Variant report

Variant	rs2335407
Chromosome Location	chr1:154843347-154843348
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	JUN	chr1:154843325-154843543	HepG2	liver:	n/a	chr1:154843404-154843417
2	SIN3A	chr1:154842513-154843365	H1-hESC	embryonic stem cell:	n/a	n/a
3	MTA3	chr1:154842372-154843495	GM12878	blood:	n/a	n/a
4	JUND	chr1:154843242-154843587	HepG2	liver:	n/a	n/a
5	HCFC1	chr1:154842654-154843397	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:154843314-154843364	AG10803	skin:	n/a
2	chr1:154843314-154843364	PANC-1	pancreas:	n/a
3	chr1:154843314-154843364	Jurkat	blood:	n/a
4	chr1:154843314-154843364	HPAEpiC	pulmonary alveolar:	n/a
5	chr1:154843314-154843364	GM06990	blood:	n/a
6	chr1:154843314-154843364	GM12878	blood:	n/a
7	chr1:154843314-154843364	BE2_C	brain:	n/a
8	chr1:154843314-154843364	ProgFib	skin:	n/a
9	chr1:154843314-154843364	HEK293	kidney:	embryo
10	chr1:154843314-154843364	HCF	heart:	n/a
11	chr1:154843314-154843364	Hela-S3	cervix:	n/a
12	chr1:154843314-154843364	A549	lung:	n/a
13	chr1:154843314-154843364	ovcar-3	ovarian:	n/a
14	chr1:154843314-154843364	HepG2	liver:	n/a
15	chr1:154843314-154843364	HIPEpiC	eye:	n/a
16	chr1:154843314-154843364	AG04449	skin:	fetal
17	chr1:154843314-154843364	HAEpiC	amniotic membrane:	n/a
18	chr1:154843314-154843364	GM12891	blood:	n/a
19	chr1:154843314-154843364	AG04450	lung:	fetal
20	chr1:154843314-154843364	IMR90	lung:	fetal
21	chr1:154843314-154843364	Hepatocyte	liver:	n/a
22	chr1:154843314-154843364	GM12892	blood:	n/a
23	chr1:154843314-154843364	HCT-116	colon:	n/a
24	chr1:154843314-154843364	SK-N-MC	brain:	n/a
25	chr1:154843314-154843364	SK-N-SH	brain:	n/a
26	chr1:154843314-154843364	HUVEC	blood vessel:	n/a
27	chr1:154843314-154843364	CMK	blood:	n/a
28	chr1:154843314-154843364	MCF10A-Er-Src	breast:	n/a
29	chr1:154843314-154843364	LNCaP	prostate:	n/a
30	chr1:154843314-154843364	AoSMC	blood vessel:	n/a
31	chr1:154843314-154843364	GM19239	blood:	n/a
32	chr1:154843314-154843364	HRPEpiC	eye:	n/a
33	chr1:154843314-154843364	SK-N-SH_RA	brain:	n/a
34	chr1:154843314-154843364	NHDF-neo	bronchial:	n/a
35	chr1:154843314-154843364	NHBE	bronchial:	n/a
36	chr1:154843314-154843364	AG09309	skin:	n/a
37	chr1:154843314-154843364	AG09319	gingival:	n/a
38	chr1:154843314-154843364	T-47D	breast:	n/a
39	chr1:154843314-154843364	NH-A	brain:	n/a
40	chr1:154843314-154843364	NT2-D1	testis:	n/a
41	chr1:154843314-154843364	HCM	heart:	n/a
42	chr1:154843314-154843364	U87	brain:	n/a
43	chr1:154843314-154843364	Caco-2	colon:	n/a
44	chr1:154843314-154843364	HL-60	blood:	n/a
45	chr1:154843314-154843364	RPTEC	kidney:	n/a
46	chr1:154843314-154843364	PrEC	prostate:	n/a
47	chr1:154843314-154843364	SKMC	muscle:	n/a
48	chr1:154843314-154843364	ECC-1	luminal epithelium:	n/a
49	chr1:154843314-154843364	SAEC	small airway:	n/a
50	chr1:154843314-154843364	K562	blood:	n/a

No data

Variant related genes	Relation type
KCNN3	TF binding region
KCNN3	CpG island

Extended variants
information (count: 84 )
Associated
traits (count: 14 )

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs1007170	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.93[TSI][hapmap];0.81[YRI][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10796934	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10796935	0.86[ASN][1000 genomes]
rs10908444	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10908445	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10908446	0.91[ASN][1000 genomes]
rs10908447	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10908448	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.86[ASN][1000 genomes]
rs1109815	0.83[ASN][1000 genomes]
rs11264276	0.84[EUR][1000 genomes]
rs11264278	0.88[ASN][1000 genomes]
rs11264280	0.81[ASN][1000 genomes]
rs11264281	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11264282	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11264283	0.91[ASN][1000 genomes]
rs11264284	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11264290	0.83[ASN][1000 genomes]
rs12036859	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12069356	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12095061	0.91[CEU][hapmap];0.83[ASN][1000 genomes]
rs12130132	0.88[CEU][hapmap];1.00[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12144978	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1580943	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1976559	0.86[ASN][1000 genomes]
rs1977879	0.86[ASN][1000 genomes]
rs2061690	0.92[CEU][hapmap];1.00[CHB][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs2102423	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2135219	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2174507	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2335408	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.91[TSI][hapmap];0.83[ASN][1000 genomes]
rs2335409	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3738026	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4240874	0.86[ASN][1000 genomes]
rs4240875	0.86[ASN][1000 genomes]
rs4339857	0.86[ASN][1000 genomes]
rs4578216	0.90[CHB][hapmap];0.95[CHD][hapmap];0.85[JPT][hapmap]
rs4845398	0.88[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4845399	0.83[EUR][1000 genomes]
rs4845400	0.91[ASN][1000 genomes]
rs4845677	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4845678	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4845679	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4845680	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4845681	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4845682	0.90[ASN][1000 genomes]
rs4845683	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4845685	0.82[ASN][1000 genomes]
rs4845687	0.87[ASN][1000 genomes]
rs4845688	0.86[ASN][1000 genomes]
rs4845689	0.86[ASN][1000 genomes]
rs4845690	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.86[ASN][1000 genomes]
rs4845691	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4845693	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.83[ASN][1000 genomes]
rs4845694	0.83[ASN][1000 genomes]
rs4845695	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4845696	0.83[ASN][1000 genomes]
rs6656435	0.90[ASN][1000 genomes]
rs6656494	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6669791	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6674853	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6683557	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6686873	0.83[ASN][1000 genomes]
rs6699043	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.91[TSI][hapmap];0.83[ASN][1000 genomes]
rs6699080	0.92[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];0.98[TSI][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs705094	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.91[TSI][hapmap];0.82[ASN][1000 genomes]
rs72702224	0.83[ASN][1000 genomes]
rs7528532	0.91[ASN][1000 genomes]
rs7531728	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7544528	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7553195	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];0.98[TSI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs869506	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.98[TSI][hapmap];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs877343	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.91[TSI][hapmap];0.83[ASN][1000 genomes]
rs883718	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs906593	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs9793588	0.84[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	nsv532579	chr1:154548165-155262692	Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	575 gene(s)	inside rSNPs	diseases
2	nsv427797	chr1:154559115-154933717	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv432931	chr1:154794318-154855055	Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
4	esv29982	chr1:154818353-154882544	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv432942	chr1:154818353-154903047	Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
6	nsv432964	chr1:154820067-154849590	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
7	nsv432953	chr1:154820067-154855055	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
8	nsv464073	chr1:154837796-154904840	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
9	nsv547960	chr1:154837796-154904840	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

mRNA abundance (count:14)

SNP	Gene	Cis/trans	Tissue	Source
rs2335407	PBXIP1	cis	lymphoblastoid	seeQTL
rs2335407	OAZ3	cis	parietal	SCAN
rs2335407	PBXIP1	Cis_1M	lymphoblastoid	RTeQTL
rs2335407	GPATCH4	cis	parietal	SCAN
rs2335407	S100A3	cis	cerebellum	SCAN
rs2335407	PBXIP1	cis	normal skin	skin_eQTL
rs2335407	RIT1	cis	cerebellum	SCAN
rs2335407	KCNN3	cis	cerebellum	SCAN
rs2335407	INTS3	cis	parietal	SCAN
rs2335407	LCE2C	cis	cerebellum	SCAN
rs2335407	ENSA	cis	parietal	SCAN
rs2335407	LCE4A	cis	parietal	SCAN
rs2335407	OTUD7B	cis	cerebellum	SCAN
rs2335407	KCNN3	cis	parietal	SCAN

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:154841600-154843400	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
2	chr1:154841800-154843400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
3	chr1:154842000-154843400	Enhancers	Primary hematopoietic stem cells	blood
4	chr1:154842000-154843400	Active TSS	Fetal Brain Female	brain
5	chr1:154842200-154843400	Bivalent Enhancer	Fetal Thymus	thymus
6	chr1:154842400-154843400	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
7	chr1:154842400-154843400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
8	chr1:154842600-154843400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:154842600-154843400	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr1:154842600-154844000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:154842800-154843400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
12	chr1:154842800-154843400	Enhancers	Esophagus	oesophagus
13	chr1:154842800-154843400	Active TSS	A549	lung
14	chr1:154842800-154844200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
15	chr1:154843000-154843400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:154843000-154843400	Flanking Active TSS	Brain Angular Gyrus	brain
17	chr1:154843000-154843400	Flanking Active TSS	Brain Anterior Caudate	brain
18	chr1:154843000-154843400	Flanking Active TSS	Brain Cingulate Gyrus	brain
19	chr1:154843000-154843400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr1:154843000-154843400	Flanking Active TSS	Brain Substantia Nigra	brain
21	chr1:154843000-154843400	Flanking Bivalent TSS/Enh	Colon Smooth Muscle	Colon
22	chr1:154843000-154843400	Flanking Active TSS	Fetal Intestine Small	intestine
23	chr1:154843000-154843400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
24	chr1:154843000-154843600	Flanking Active TSS	GM12878-XiMat	blood
25	chr1:154843200-154843400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr1:154843200-154843400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr1:154843200-154843400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr1:154843200-154843400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr1:154843200-154843400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr1:154843200-154843400	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr1:154843200-154843400	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr1:154843200-154843400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr1:154843200-154843400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:154843200-154843400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr1:154843200-154843400	Enhancers	Brain Germinal Matrix	brain
36	chr1:154843200-154843400	Enhancers	Brain Hippocampus Middle	brain
37	chr1:154843200-154843400	Enhancers	Duodenum Smooth Muscle	Duodenum
38	chr1:154843200-154843400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
39	chr1:154843200-154843400	Enhancers	Left Ventricle	heart
40	chr1:154843200-154843400	Enhancers	Pancreas	Pancrea
41	chr1:154843200-154843400	Enhancers	Rectal Smooth Muscle	rectum
42	chr1:154843200-154843400	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr1:154843200-154843600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr1:154843200-154843600	Enhancers	Fetal Brain Male	brain
45	chr1:154843200-154843600	Enhancers	Fetal Heart	heart
46	chr1:154843200-154843600	Bivalent Enhancer	HepG2	liver
47	chr1:154843200-154843800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr1:154843200-154844000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr1:154843200-154844000	Enhancers	Duodenum Mucosa	Duodenum
50	chr1:154843200-154844200	Enhancers	H9 Cell Line	embryonic stem cell

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