Variant report

Variant	rs852531
Chromosome Location	chr7:5597677-5597678
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:94)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:94 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	PAX5	chr7:5597574-5597907	GM12892	blood:	n/a	n/a
2	NFYB	chr7:5597513-5597812	GM12878	blood:	n/a	n/a
3	TCF3	chr7:5597569-5597831	GM12878	blood:	n/a	chr7:5597764-5597774
4	RCOR1	chr7:5597309-5598000	GM12878	blood:	n/a	n/a
5	POLR2A	chr7:5597455-5597768	MCF-7	breast:	n/a	n/a
6	POLR2A	chr7:5597340-5597856	GM12891	blood:	n/a	n/a
7	POLR2A	chr7:5597400-5597874	HepG2	liver:	n/a	n/a
8	RELA	chr7:5597318-5598902	GM15510	blood:	n/a	n/a
9	POLR2A	chr7:5597284-5597742	K562	blood:	n/a	n/a
10	MXI1	chr7:5597676-5597771	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr7:5597324-5598006	GM12892	blood:	n/a	n/a
12	ZEB1	chr7:5597635-5598043	GM12878	blood:	n/a	n/a
13	BCLAF1	chr7:5597124-5598370	GM12878	blood:	n/a	n/a
14	RCOR1	chr7:5597452-5597782	HepG2	liver:	n/a	n/a
15	ATF2	chr7:5597094-5598321	GM12878	blood:	n/a	n/a
16	POLR2A	chr7:5597382-5597885	GM12878	blood:	n/a	n/a
17	NFIC	chr7:5597598-5598814	GM12878	blood:	n/a	n/a
18	RUNX3	chr7:5596921-5598171	GM12878	blood:	n/a	n/a
19	POLR2A	chr7:5597191-5598008	GM19099	blood:	n/a	n/a
20	POLR2A	chr7:5597423-5598076	GM12891	blood:	n/a	n/a
21	MTA3	chr7:5593891-5599216	GM12878	blood:	n/a	n/a
22	FOXM1	chr7:5597576-5598947	GM12878	blood:	n/a	n/a
23	POLR2A	chr7:5597587-5597964	GM10847	blood:	n/a	n/a
24	SMC3	chr7:5597635-5597690	K562	blood:	n/a	n/a
25	POLR2A	chr7:5597371-5597912	HepG2	liver:	n/a	n/a
26	NRF1	chr7:5597383-5598057	GM12878	blood:	n/a	n/a
27	POLR2A	chr7:5597364-5598021	GM18951	blood:	n/a	n/a
28	BCLAF1	chr7:5597481-5598899	GM12878	blood:	n/a	n/a
29	POLR2A	chr7:5597341-5598003	GM19193	blood:	n/a	n/a
30	MAX	chr7:5597589-5597867	HepG2	liver:	n/a	n/a
31	MEF2A	chr7:5597643-5598212	GM12878	blood:	n/a	chr7:5597943-5597957 chr7:5597944-5597955 chr7:5597942-5597957
32	ELF1	chr7:5597295-5597965	GM12878	blood:	n/a	n/a
33	MEF2A	chr7:5597612-5598112	GM12878	blood:	n/a	chr7:5597943-5597957 chr7:5597944-5597955 chr7:5597942-5597957
34	TBP	chr7:5597551-5597758	HepG2	liver:	n/a	n/a
35	RXRA	chr7:5597367-5597831	HepG2	liver:	n/a	chr7:5597432-5597446
36	POLR2A	chr7:5597305-5598136	Raji	blood:	n/a	n/a
37	MAX	chr7:5597543-5597918	K562	blood:	n/a	n/a
38	PML	chr7:5596992-5599062	GM12878	blood:	n/a	chr7:5598607-5598615
39	MYC	chr7:5597636-5597694	K562	blood:	n/a	n/a
40	EBF1	chr7:5597115-5598927	GM12878	blood:	n/a	chr7:5598706-5598717 chr7:5598707-5598716 chr7:5597441-5597450 chr7:5597441-5597450
41	POLR2A	chr7:5597549-5597761	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr7:5597175-5597975	PANC-1	pancreas:	n/a	n/a
43	BRCA1	chr7:5597650-5597783	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr7:5597031-5598031	GM18505	blood:	n/a	n/a
45	EP300	chr7:5597647-5597801	K562	blood:	n/a	chr7:5597732-5597748
46	MAZ	chr7:5597502-5597780	Hela-S3	cervix:	n/a	n/a
47	BHLHE40	chr7:5597477-5597798	K562	blood:	n/a	chr7:5597517-5597533
48	CUX1	chr7:5597472-5597700	K562	blood:	n/a	n/a
49	RELA	chr7:5597633-5598962	GM18951	blood:	n/a	n/a
50	POLR2A	chr7:5597164-5597867	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5597647-5597697	HUVEC	blood vessel:	n/a
2	chr7:5597647-5597697	SKMC	muscle:	n/a
3	chr7:5597647-5597697	HPAEpiC	pulmonary alveolar:	n/a
4	chr7:5597647-5597697	HIPEpiC	eye:	n/a
5	chr7:5597647-5597697	RPTEC	kidney:	n/a
6	chr7:5597647-5597697	Caco-2	colon:	n/a
7	chr7:5597647-5597697	NT2-D1	testis:	n/a
8	chr7:5597647-5597697	GM12878	blood:	n/a
9	chr7:5597647-5597697	MCF10A-Er-Src	breast:	n/a
10	chr7:5597647-5597697	HRCEpiC	kidney:	n/a
11	chr7:5597647-5597697	SK-N-MC	brain:	n/a
12	chr7:5597647-5597697	AG10803	skin:	n/a
13	chr7:5597647-5597697	T-47D	breast:	n/a
14	chr7:5597647-5597697	Hepatocyte	liver:	n/a
15	chr7:5597647-5597697	AG04450	lung:	fetal
16	chr7:5597647-5597697	GM19239	blood:	n/a
17	chr7:5597647-5597697	HepG2	liver:	n/a
18	chr7:5597647-5597697	GM12891	blood:	n/a
19	chr7:5597647-5597697	NB4	blood:	n/a
20	chr7:5597647-5597697	HEK293	kidney:	embryo
21	chr7:5597647-5597697	BJ	skin:	n/a
22	chr7:5597647-5597697	H1-hESC	embryonic stem cell:	embryo
23	chr7:5597647-5597697	NHBE	bronchial:	n/a
24	chr7:5597647-5597697	CMK	blood:	n/a
25	chr7:5597647-5597697	A549	lung:	n/a
26	chr7:5597647-5597697	LNCaP	prostate:	n/a
27	chr7:5597647-5597697	HCF	heart:	n/a
28	chr7:5597647-5597697	HCM	heart:	n/a
29	chr7:5597647-5597697	ovcar-3	ovarian:	n/a
30	chr7:5597647-5597697	HEEpiC	esophagus:	n/a
31	chr7:5597647-5597697	PrEC	prostate:	n/a
32	chr7:5597647-5597697	NH-A	brain:	n/a
33	chr7:5597647-5597697	NHDF-neo	bronchial:	n/a
34	chr7:5597647-5597697	HMEC	breast:	n/a
35	chr7:5597647-5597697	SK-N-SH	brain:	n/a
36	chr7:5597647-5597697	HL-60	blood:	n/a
37	chr7:5597647-5597697	MCF-7	breast:	n/a
38	chr7:5597647-5597697	AoSMC	blood vessel:	n/a
39	chr7:5597647-5597697	PANC-1	pancreas:	n/a
40	chr7:5597647-5597697	AG09319	gingival:	n/a
41	chr7:5597647-5597697	AG09309	skin:	n/a
42	chr7:5597647-5597697	AG04449	skin:	fetal
43	chr7:5597647-5597697	GM12892	blood:	n/a
44	chr7:5597647-5597697	SK-N-SH_RA	brain:	n/a
45	chr7:5597647-5597697	BE2_C	brain:	n/a
46	chr7:5597647-5597697	SAEC	small airway:	n/a
47	chr7:5597647-5597697	ECC-1	luminal epithelium:	n/a
48	chr7:5597647-5597697	IMR90	lung:	fetal
49	chr7:5597647-5597697	HNPCEpiC	eye:	n/a
50	chr7:5597647-5597697	Jurkat	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:5595299..5597821-chr7:5720043..5723343,4	MCF-7	breast:
2	chr7:5531500..5533509-chr7:5596398..5598659,2	K562	blood:
3	chr7:5533565..5537610-chr7:5594791..5600448,10	K562	blood:
4	chr7:5558806..5574463-chr7:5583405..5604290,160	MCF-7	breast:
5	chr7:5597090..5598999-chr7:5725953..5728354,2	K562	blood:
6	chr7:5569623..5570567-chr7:5597254..5598015,2	Hela-S3	cervix:
7	chr7:5597370..5600329-chr7:5734378..5736141,2	MCF-7	breast:
8	chr7:5532197..5537592-chr7:5593884..5603950,17	MCF-7	breast:
9	chr7:5464910..5469932-chr7:5594160..5600416,10	MCF-7	breast:
10	chr7:5538898..5541659-chr7:5596003..5598551,3	MCF-7	breast:
11	chr7:5551753..5555420-chr7:5594196..5597835,12	MCF-7	breast:
12	chr7:5564910..5565621-chr7:5597124..5597898,2	Hela-S3	cervix:
13	chr7:5531499..5540573-chr7:5594200..5602257,20	MCF-7	breast:
14	chr7:5595916..5598684-chr7:5631829..5634716,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000228974	TF binding region
ENSG00000228974	CpG island
ENSG00000207973	Chromatin interaction
ENSG00000272953	Chromatin interaction
ENSG00000234432	Chromatin interaction
ENSG00000273084	Chromatin interaction
ENSG00000182095	Chromatin interaction
ENSG00000075624	Chromatin interaction
ENSG00000237738	Chromatin interaction
ENSG00000075618	Chromatin interaction
ENSG00000263900	Chromatin interaction
ENSG00000155034	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10245763	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1101247	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28568629	0.89[ASN][1000 genomes]
rs852493	0.82[AMR][1000 genomes]
rs852498	0.93[ASN][1000 genomes]
rs852499	0.87[ASN][1000 genomes]
rs852500	0.93[ASN][1000 genomes]
rs852502	0.89[ASN][1000 genomes]
rs852507	0.89[ASN][1000 genomes]
rs852510	0.90[ASN][1000 genomes]
rs852512	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs852526	0.85[ASN][1000 genomes]
rs852527	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs852529	0.93[ASN][1000 genomes]
rs852530	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs852532	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs852533	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 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	nsv887407	chr7:5432672-5605130	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	302 gene(s)	inside rSNPs	diseases
10	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
11	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
12	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
13	nsv887413	chr7:5521468-5607884	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	279 gene(s)	inside rSNPs	diseases
14	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
15	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
16	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
17	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
18	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
19	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
20	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

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5594800-5598600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
2	chr7:5594800-5598800	Flanking Active TSS	Primary B cells from peripheral blood	blood
3	chr7:5594800-5599000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
4	chr7:5596200-5598600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:5596200-5598600	Enhancers	Fetal Heart	heart
6	chr7:5596200-5598600	Enhancers	Fetal Lung	lung
7	chr7:5596400-5598600	Flanking Active TSS	Primary B cells from cord blood	blood
8	chr7:5596400-5598600	Flanking Active TSS	Primary hematopoietic stem cells	blood
9	chr7:5596400-5598600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
10	chr7:5596400-5598600	Flanking Active TSS	GM12878-XiMat	blood
11	chr7:5596400-5598600	Flanking Active TSS	Hela-S3	cervix
12	chr7:5596400-5598800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
13	chr7:5596400-5599000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr7:5596400-5599000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
15	chr7:5596400-5599000	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr7:5596400-5599000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr7:5596400-5599800	Enhancers	Spleen	Spleen
18	chr7:5596400-5601800	Weak transcription	Ovary	ovary
19	chr7:5596600-5598000	Flanking Active TSS	A549	lung
20	chr7:5596600-5598200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr7:5596600-5598600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr7:5596600-5598600	Flanking Active TSS	Colon Smooth Muscle	Colon
23	chr7:5596600-5598600	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
24	chr7:5596600-5598600	Enhancers	Fetal Intestine Large	intestine
25	chr7:5596600-5598600	Enhancers	HMEC	breast
26	chr7:5596600-5598600	Enhancers	HSMMtube	muscle
27	chr7:5596600-5598600	Enhancers	NHDF-Ad	bronchial
28	chr7:5596600-5598800	Enhancers	Placenta	Placenta
29	chr7:5596600-5598800	Flanking Active TSS	Stomach Smooth Muscle	stomach
30	chr7:5596600-5599000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:5596600-5599000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr7:5596600-5599000	Enhancers	Esophagus	oesophagus
33	chr7:5596600-5599000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr7:5596600-5599000	Enhancers	HUVEC	blood vessel
35	chr7:5596600-5601800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr7:5596600-5601800	Weak transcription	Fetal Kidney	kidney
37	chr7:5596800-5597800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:5596800-5597800	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr7:5596800-5597800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr7:5596800-5598000	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr7:5596800-5598200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr7:5596800-5598200	Weak transcription	Brain Germinal Matrix	brain
43	chr7:5596800-5598200	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr7:5596800-5598400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr7:5596800-5598400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr7:5596800-5598400	Enhancers	Gastric	stomach
47	chr7:5596800-5598600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr7:5596800-5598600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr7:5596800-5598600	Enhancers	Fetal Intestine Small	intestine
50	chr7:5596800-5598600	Enhancers	Left Ventricle	heart

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