Variant report

Variant	rs73334455
Chromosome Location	chr7:5631192-5631193
allele	A/G/T
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	EBF1	chr7:5631144-5631633	GM12878	blood:	n/a	chr7:5631418-5631428
2	RAD21	chr7:5631181-5631845	Hela-S3	cervix:	n/a	chr7:5631701-5631720 chr7:5631702-5631711
3	EGR1	chr7:5631068-5631911	HCT-116	colon:	n/a	chr7:5631438-5631452 chr7:5631512-5631522 chr7:5631513-5631523 chr7:5631423-5631437 chr7:5631691-5631704
4	CHD1	chr7:5631009-5636685	IMR90	lung:	n/a	chr7:5633559-5633569 chr7:5633779-5633789 chr7:5634268-5634278 chr7:5634031-5634041 chr7:5632211-5632221
5	MAX	chr7:5631171-5631620	ECC-1	luminal epithelium:	n/a	n/a
6	POLR2A	chr7:5631134-5631443	HUVEC	blood vessel:	n/a	n/a
7	POLR2A	chr7:5630820-5631574	SK-N-SH	brain:	n/a	n/a
8	POLR2A	chr7:5631083-5631390	HUVEC	blood vessel:	n/a	n/a
9	EP300	chr7:5631190-5631587	GM12878	blood:	n/a	n/a
10	TEAD4	chr7:5631056-5631597	HepG2	liver:	n/a	n/a
11	BRCA1	chr7:5631004-5631679	Hela-S3	cervix:	n/a	n/a
12	SMARCC1	chr7:5631037-5632048	Hela-S3	cervix:	n/a	n/a
13	TEAD4	chr7:5631032-5631690	ECC-1	luminal epithelium:	n/a	n/a
14	RELA	chr7:5631066-5631560	GM19193	blood:	n/a	n/a
15	SMARCB1	chr7:5631057-5636588	Hela-S3	cervix:	n/a	n/a
16	STAT1	chr7:5631158-5631583	GM12878	blood:	n/a	n/a
17	SP1	chr7:5630941-5631979	A549	lung:	n/a	chr7:5631090-5631100 chr7:5631437-5631447 chr7:5631479-5631493
18	GATA3	chr7:5630954-5631775	A549	lung:	n/a	n/a
19	TFAP2C	chr7:5630812-5631796	Hela-S3	cervix:	n/a	n/a
20	RELA	chr7:5631179-5631643	GM10847	blood:	n/a	n/a
21	TCF12	chr7:5631002-5633216	A549	lung:	n/a	chr7:5631342-5631350
22	REST	chr7:5631136-5631563	SK-N-SH	brain:	n/a	chr7:5631528-5631542
23	CHD2	chr7:5631068-5631792	Hela-S3	cervix:	n/a	n/a
24	TEAD4	chr7:5630844-5631650	K562	blood:	n/a	n/a
25	EBF1	chr7:5631163-5631475	GM12878	blood:	n/a	chr7:5631418-5631428
26	ELF1	chr7:5631025-5633525	GM12878	blood:	n/a	n/a
27	REST	chr7:5631082-5631563	SK-N-SH	brain:	n/a	chr7:5631528-5631542
28	TEAD4	chr7:5630725-5631817	SK-N-SH	brain:	n/a	n/a
29	RUNX3	chr7:5630755-5631640	GM12878	blood:	n/a	chr7:5631320-5631335
30	TEAD4	chr7:5631075-5631608	H1-hESC	embryonic stem cell:	n/a	n/a
31	SPI1	chr7:5631144-5631647	HL-60	blood:	n/a	chr7:5631405-5631418 chr7:5631405-5631418
32	TCF7L2	chr7:5631108-5631398	PANC-1	pancreas:	n/a	n/a
33	NFIC	chr7:5631119-5631669	GM12878	blood:	n/a	n/a
34	MAFK	chr7:5631164-5632657	Hela-S3	cervix:	n/a	chr7:5631755-5631765 chr7:5631407-5631422
35	MXI1	chr7:5630851-5636675	IMR90	lung:	n/a	n/a
36	TEAD4	chr7:5631081-5631657	A549	lung:	n/a	n/a
37	MAX	chr7:5630766-5631598	SK-N-SH	brain:	n/a	n/a
38	NFIC	chr7:5630705-5631782	SK-N-SH	brain:	n/a	chr7:5631041-5631058
39	EP300	chr7:5630932-5631509	SK-N-SH_RA	brain:	n/a	n/a
40	TAF1	chr7:5630913-5631451	SK-N-SH	brain:	n/a	n/a
41	TEAD4	chr7:5631066-5631602	K562	blood:	n/a	n/a
42	RFX5	chr7:5630939-5632667	Hela-S3	cervix:	n/a	chr7:5631324-5631339 chr7:5631099-5631108 chr7:5631096-5631110
43	MAX	chr7:5630974-5631676	A549	lung:	n/a	n/a
44	PAX5	chr7:5631173-5631565	GM12878	blood:	n/a	n/a
45	SIN3AK20	chr7:5630743-5631618	SK-N-SH	brain:	n/a	n/a
46	GATA3	chr7:5630334-5631762	SK-N-SH	brain:	n/a	chr7:5630637-5630646
47	POLR2A	chr7:5631124-5631451	HUVEC	blood vessel:	n/a	n/a
48	NFIC	chr7:5630900-5631667	GM12878	blood:	n/a	chr7:5631041-5631058
49	EP300	chr7:5630984-5631683	A549	lung:	n/a	n/a
50	NR3C1	chr7:5631147-5631529	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5631189-5631239	HPAEpiC	pulmonary alveolar:	n/a
2	chr7:5631189-5631239	MCF10A-Er-Src	breast:	n/a
3	chr7:5631189-5631239	HCM	heart:	n/a
4	chr7:5631189-5631239	HEEpiC	esophagus:	n/a
5	chr7:5631189-5631239	HNPCEpiC	eye:	n/a
6	chr7:5631189-5631239	SK-N-MC	brain:	n/a
7	chr7:5631189-5631239	LNCaP	prostate:	n/a
8	chr7:5631189-5631239	PANC-1	pancreas:	n/a
9	chr7:5631189-5631239	HUVEC	blood vessel:	n/a
10	chr7:5631189-5631239	BE2_C	brain:	n/a
11	chr7:5631189-5631239	U87	brain:	n/a
12	chr7:5631189-5631239	T-47D	breast:	n/a
13	chr7:5631189-5631239	NHBE	bronchial:	n/a
14	chr7:5631189-5631239	AG09319	gingival:	n/a
15	chr7:5631189-5631239	HIPEpiC	eye:	n/a
16	chr7:5631189-5631239	NT2-D1	testis:	n/a
17	chr7:5631189-5631239	GM06990	blood:	n/a
18	chr7:5631189-5631239	Caco-2	colon:	n/a
19	chr7:5631189-5631239	AG09309	skin:	n/a
20	chr7:5631189-5631239	A549	lung:	n/a
21	chr7:5631189-5631239	GM12892	blood:	n/a
22	chr7:5631189-5631239	Jurkat	blood:	n/a
23	chr7:5631189-5631239	HRCEpiC	kidney:	n/a
24	chr7:5631189-5631239	BJ	skin:	n/a
25	chr7:5631189-5631239	ECC-1	luminal epithelium:	n/a
26	chr7:5631189-5631239	HCF	heart:	n/a
27	chr7:5631189-5631239	SAEC	small airway:	n/a
28	chr7:5631189-5631239	CMK	blood:	n/a
29	chr7:5631189-5631239	AG04450	lung:	fetal
30	chr7:5631189-5631239	HepG2	liver:	n/a
31	chr7:5631189-5631239	SKMC	muscle:	n/a
32	chr7:5631189-5631239	AoSMC	blood vessel:	n/a
33	chr7:5631189-5631239	ProgFib	skin:	n/a
34	chr7:5631189-5631239	ovcar-3	ovarian:	n/a
35	chr7:5631189-5631239	H1-hESC	embryonic stem cell:	embryo
36	chr7:5631189-5631239	HRPEpiC	eye:	n/a
37	chr7:5631189-5631239	HMEC	breast:	n/a
38	chr7:5631189-5631239	NH-A	brain:	n/a
39	chr7:5631189-5631239	GM19239	blood:	n/a
40	chr7:5631189-5631239	HEK293	kidney:	embryo
41	chr7:5631189-5631239	AG04449	skin:	fetal
42	chr7:5631189-5631239	PFSK-1	brain:	n/a
43	chr7:5631189-5631239	GM12878	blood:	n/a
44	chr7:5631189-5631239	HL-60	blood:	n/a
45	chr7:5631189-5631239	Hepatocyte	liver:	n/a
46	chr7:5631189-5631239	NHDF-neo	bronchial:	n/a
47	chr7:5631189-5631239	MCF-7	breast:	n/a
48	chr7:5631189-5631239	HCT-116	colon:	n/a
49	chr7:5631189-5631239	SK-N-SH_RA	brain:	n/a
50	chr7:5631189-5631239	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:5551336..5555391-chr7:5631153..5637818,11	K562	blood:
2	chr7:5568810..5571119-chr7:5631190..5634069,5	MCF-7	breast:
3	chr7:5601206..5603452-chr7:5630242..5632933,3	MCF-7	breast:
4	chr7:5630491..5634130-chr7:5717559..5720896,4	K562	blood:
5	chr7:5534332..5536229-chr7:5631160..5633619,2	MCF-7	breast:
6	chr7:5563317..5574038-chr7:5630450..5643029,58	K562	blood:
7	chr7:5533112..5541360-chr7:5629989..5636364,13	K562	blood:

Variant related genes	Relation type
FSCN1	TF binding region
FSCN1	CpG island
ENSG00000075624	Chromatin interaction
ENSG00000207973	Chromatin interaction
ENSG00000155034	Chromatin interaction
ENSG00000263900	Chromatin interaction
ENSG00000237738	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs73334439	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73334446	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73334454	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73334473	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869165	chr7:4889618-5799719	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	352 gene(s)	inside rSNPs	diseases
2	nsv530979	chr7:5101631-5864814	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
3	nsv530981	chr7:5157150-5920006	Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	348 gene(s)	inside rSNPs	diseases
4	esv1814049	chr7:5314993-5675131	Active TSS Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	333 gene(s)	inside rSNPs	diseases
5	esv1820266	chr7:5332088-5665173	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
6	nsv530983	chr7:5370746-6070852	Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	368 gene(s)	inside rSNPs	diseases
7	nsv887404	chr7:5402606-5667645	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	331 gene(s)	inside rSNPs	diseases
8	nsv916391	chr7:5417945-5889565	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	336 gene(s)	inside rSNPs	diseases
9	nsv887408	chr7:5432672-5667645	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription 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	331 gene(s)	inside rSNPs	diseases
10	nsv830890	chr7:5464933-5705158	Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
11	nsv533108	chr7:5488018-6316581	Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	390 gene(s)	inside rSNPs	diseases
12	nsv1025434	chr7:5537571-5705283	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	297 gene(s)	inside rSNPs	diseases
13	nsv482449	chr7:5557585-5743673	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	294 gene(s)	inside rSNPs	diseases
14	nsv1033556	chr7:5565080-6186815	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	357 gene(s)	inside rSNPs	diseases
15	nsv538710	chr7:5565080-6186815	Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh 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	357 gene(s)	inside rSNPs	diseases
16	nsv887414	chr7:5584934-5667645	Flanking Bivalent TSS/Enh Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
17	nsv887415	chr7:5584934-5675305	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
18	nsv887416	chr7:5584934-5695259	Genic enhancers Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
19	nsv530467	chr7:5617816-5815082	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
20	nsv1017612	chr7:5629728-5819144	Genic enhancers Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
21	nsv1021989	chr7:5629728-6186815	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
22	esv3411018	chr7:5630951-5633799	Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5621000-5631200	Weak transcription	Right Ventricle	heart
2	chr7:5621000-5631600	Weak transcription	Pancreas	Pancrea
3	chr7:5621200-5631400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr7:5624400-5631200	Weak transcription	Adipose Nuclei	Adipose
5	chr7:5625000-5631200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr7:5626200-5631600	Weak transcription	Brain Angular Gyrus	brain
7	chr7:5626800-5631200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr7:5627000-5631200	Weak transcription	Brain Anterior Caudate	brain
9	chr7:5628400-5631200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr7:5628400-5631200	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr7:5629200-5631200	Enhancers	Brain Hippocampus Middle	brain
12	chr7:5629400-5631200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:5629400-5631200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:5629400-5631600	Enhancers	Brain Substantia Nigra	brain
15	chr7:5629400-5632400	Enhancers	Primary hematopoietic stem cells	blood
16	chr7:5629600-5631200	Enhancers	Placenta	Placenta
17	chr7:5629600-5631600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr7:5629600-5631600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr7:5629600-5632000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr7:5629800-5631200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr7:5629800-5632400	Enhancers	Spleen	Spleen
22	chr7:5630000-5631200	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr7:5630000-5631600	Weak transcription	Esophagus	oesophagus
24	chr7:5630200-5631200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr7:5630200-5631600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr7:5630200-5631800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr7:5630400-5633200	Enhancers	Fetal Heart	heart
28	chr7:5630600-5631400	Enhancers	Muscle Satellite Cultured Cells	--
29	chr7:5630600-5631600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr7:5630600-5632400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr7:5630800-5631200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
32	chr7:5630800-5631200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr7:5630800-5631200	Enhancers	Fetal Muscle Leg	muscle
34	chr7:5630800-5631200	Enhancers	Osteobl	bone
35	chr7:5630800-5631600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr7:5630800-5631600	Enhancers	GM12878-XiMat	blood
37	chr7:5630800-5631600	Enhancers	HMEC	breast
38	chr7:5630800-5631800	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr7:5630800-5631800	Enhancers	HUVEC	blood vessel
40	chr7:5630800-5632000	Enhancers	NHDF-Ad	bronchial
41	chr7:5631000-5631200	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
42	chr7:5631000-5631200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr7:5631000-5631200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:5631000-5631200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr7:5631000-5631200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr7:5631000-5631200	Enhancers	K562	blood
47	chr7:5631000-5631200	Enhancers	NH-A	brain
48	chr7:5631000-5631600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
49	chr7:5631000-5631600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr7:5631000-5631600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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