Variant report

Variant	esv3493691
Chromosome Location	chr7:12628257-12634980
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:123)
CpG islands
(count:367)
Chromatin interactive
region (count:7)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:12630263-12630542	K562	blood:	n/a	n/a
2	BHLHE40	chr7:12627895-12628444	K562	blood:	n/a	n/a
3	BHLHE40	chr7:12634844-12635148	K562	blood:	n/a	n/a
4	BHLHE40	chr7:12630354-12630389	K562	blood:	n/a	n/a
5	CBX3	chr7:12627894-12628692	K562	blood:	n/a	n/a
6	CBX3	chr7:12630165-12630543	K562	blood:	n/a	n/a
7	CBX3	chr7:12633685-12634028	K562	blood:	n/a	n/a
8	CEBPB	chr7:12628718-12628942	IMR90	lung:	n/a	n/a
9	CEBPB	chr7:12628630-12628939	A549	lung:	n/a	n/a
10	CEBPB	chr7:12630378-12630397	K562	blood:	n/a	n/a
11	CEBPB	chr7:12628547-12628938	K562	blood:	n/a	n/a
12	CEBPB	chr7:12628625-12628909	MCF-7	breast:	n/a	n/a
13	CEBPB	chr7:12628122-12628421	K562	blood:	n/a	n/a
14	CEBPB	chr7:12628699-12628936	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr7:12628632-12628949	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:12628521-12628964	K562	blood:	n/a	n/a
17	CEBPD	chr7:12628238-12628465	K562	blood:	n/a	n/a
18	CHD2	chr7:12633841-12633874	K562	blood:	n/a	n/a
19	CTCF	chr7:12634806-12634856	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr7:12634820-12634970	HepG2	liver:	n/a	n/a
21	CTCF	chr7:12634700-12634850	Caco-2	colon:	n/a	n/a
22	CTCF	chr7:12628842-12628899	Pancreas_OC	pancreas:	n/a	n/a
23	CTCF	chr7:12628680-12628830	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr7:12628948-12628980	GM13977	blood:	n/a	n/a
25	EGR1	chr7:12628217-12628610	K562	blood:	n/a	n/a
26	EP300	chr7:12630183-12630569	K562	blood:	n/a	n/a
27	EP300	chr7:12634853-12635135	K562	blood:	n/a	n/a
28	EP300	chr7:12634827-12635144	T-47D	breast:	n/a	n/a
29	EP300	chr7:12634288-12634295	K562	blood:	n/a	n/a
30	EP300	chr7:12627932-12628436	K562	blood:	n/a	n/a
31	ESR1	chr7:12634678-12635215	T-47D	breast:	n/a	n/a
32	ESR1	chr7:12634718-12635207	T-47D	breast:	n/a	n/a
33	ESR1	chr7:12634743-12635231	T-47D	breast:	n/a	n/a
34	ESR1	chr7:12628159-12628476	T-47D	breast:	n/a	n/a
35	ESR1	chr7:12634776-12635193	T-47D	breast:	n/a	n/a
36	ESR1	chr7:12634755-12635233	T-47D	breast:	n/a	n/a
37	ESR1	chr7:12628218-12628455	T-47D	breast:	n/a	n/a
38	ESR1	chr7:12634865-12635094	T-47D	breast:	n/a	n/a
39	FOS	chr7:12633791-12634114	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr7:12633839-12634059	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr7:12633814-12634095	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr7:12633801-12634084	MCF10A-Er-Src	breast:	n/a	n/a
43	GABPA	chr7:12630279-12630531	K562	blood:	n/a	n/a
44	GATA2	chr7:12634846-12635195	K562	blood:	n/a	n/a
45	GATA2	chr7:12630158-12630590	K562	blood:	n/a	n/a
46	GATA2	chr7:12628167-12628466	K562	blood:	n/a	n/a
47	GATA3	chr7:12634743-12635204	MCF-7	breast:	n/a	chr7:12635038-12635046
48	GATA3	chr7:12634735-12635218	T-47D	breast:	n/a	chr7:12635038-12635046
49	GATA3	chr7:12634869-12635089	MCF-7	breast:	n/a	chr7:12635038-12635046
50	IRF1	chr7:12630333-12630579	K562	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12629167-12629217	SK-N-MC	brain:	n/a
2	chr7:12629167-12629217	SK-N-MC	brain:	n/a
3	chr7:12629275-12629325	Hepatocyte	liver:	n/a
4	chr7:12628568-12628618	NB4	blood:	n/a
5	chr7:12628568-12628618	Jurkat	blood:	n/a
6	chr7:12629167-12629217	RPTEC	kidney:	n/a
7	chr7:12628568-12628618	GM19239	blood:	n/a
8	chr7:12633679-12633729	H1-hESC	embryonic stem cell:	embryo
9	chr7:12628568-12628618	HRE	kidney:	n/a
10	chr7:12629127-12629177	GM19239	blood:	n/a
11	chr7:12628568-12628618	PrEC	prostate:	n/a
12	chr7:12628568-12628618	NHDF-neo	bronchial:	n/a
13	chr7:12629275-12629325	ProgFib	skin:	n/a
14	chr7:12633679-12633729	HNPCEpiC	eye:	n/a
15	chr7:12629275-12629325	Caco-2	colon:	n/a
16	chr7:12629167-12629217	NHDF-neo	bronchial:	n/a
17	chr7:12633679-12633729	NHDF-neo	bronchial:	n/a
18	chr7:12628568-12628618	HRPEpiC	eye:	n/a
19	chr7:12633679-12633729	SAEC	small airway:	n/a
20	chr7:12628568-12628618	NH-A	brain:	n/a
21	chr7:12633679-12633729	ovcar-3	ovarian:	n/a
22	chr7:12629127-12629177	NT2-D1	testis:	n/a
23	chr7:12629127-12629177	Caco-2	colon:	n/a
24	chr7:12629275-12629325	HEEpiC	esophagus:	n/a
25	chr7:12629275-12629325	SAEC	small airway:	n/a
26	chr7:12629275-12629325	GM12891	blood:	n/a
27	chr7:12628568-12628618	CMK	blood:	n/a
28	chr7:12629275-12629325	HCM	heart:	n/a
29	chr7:12629275-12629325	HIPEpiC	eye:	n/a
30	chr7:12628677-12628727	H1-hESC	embryonic stem cell:	embryo
31	chr7:12629127-12629177	HRE	kidney:	n/a
32	chr7:12633679-12633729	PrEC	prostate:	n/a
33	chr7:12633679-12633729	HCF	heart:	n/a
34	chr7:12628568-12628618	HEK293	kidney:	embryo
35	chr7:12633679-12633729	IMR90	lung:	fetal
36	chr7:12629275-12629325	U87	brain:	n/a
37	chr7:12628568-12628618	NHBE	bronchial:	n/a
38	chr7:12629167-12629217	HCT-116	colon:	n/a
39	chr7:12629275-12629325	HRCEpiC	kidney:	n/a
40	chr7:12633679-12633729	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:12629127-12629177	LNCaP	prostate:	n/a
42	chr7:12629127-12629177	CMK	blood:	n/a
43	chr7:12629127-12629177	Hela-S3	cervix:	n/a
44	chr7:12629167-12629217	BJ	skin:	n/a
45	chr7:12629167-12629217	AG04450	lung:	fetal
46	chr7:12629275-12629325	SK-N-MC	brain:	n/a
47	chr7:12628677-12628727	GM06990	blood:	n/a
48	chr7:12629127-12629177	A549	lung:	n/a
49	chr7:12629127-12629177	PrEC	prostate:	n/a
50	chr7:12629127-12629177	IMR90	lung:	fetal

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:12632374..12633925-chr7:12635671..12637627,2	MCF-7	breast:
2	chr7:12628422..12631395-chr7:12632472..12635866,3	K562	blood:
3	chr7:12623803..12625558-chr7:12629908..12631864,2	K562	blood:
4	chr7:12627909..12630200-chr7:12630367..12632328,2	MCF-7	breast:
5	chr7:12620852..12624352-chr7:12625661..12628427,3	K562	blood:
6	chr7:12628422..12631395-chr7:12632472..12635866,3	K562	blood:
7	chr7:12623803..12627040-chr7:12629908..12631864,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VWDE-2	chr7:12634585-12634824	ENSG00000248523
2	lnc-VWDE-2	chr7:12628112-12628690	ENSG00000248523
3	lnc-VWDE-2	chr7:12632501-12632676	ENSG00000248523

No data

Variant related genes	Relation type
SCIN	TF binding region
SCIN	CpG island
ENSG00000006747	chromatin interactions
HMGA2	miRNA target sites

Extended variants
information (count: 365 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:365 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368397186	chr7:12628264-12628265	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs17136712	chr7:12628341-12628342	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs73293093	chr7:12628369-12628370	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs555114311	chr7:12628404-12628405	Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs13202	chr7:12628410-12628411	Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs553448298	chr7:12628433-12628434	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs112614850	chr7:12628436-12628437	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs201706818	chr7:12628458-12628459	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs373506714	chr7:12628459-12628460	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs62448298	chr7:12628463-12628464	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs571850899	chr7:12628465-12628466	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs542218764	chr7:12628490-12628491	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs571479288	chr7:12628534-12628535	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs575044482	chr7:12628535-12628536	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs14001	chr7:12628560-12628561	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs116787461	chr7:12628574-12628575	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs76236833	chr7:12628577-12628578	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs562483223	chr7:12628578-12628579	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs11976	chr7:12628587-12628588	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs550795519	chr7:12628592-12628593	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs368622422	chr7:12628597-12628598	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs146914885	chr7:12628630-12628631	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs567777281	chr7:12628642-12628643	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs114900863	chr7:12628760-12628761	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs192194452	chr7:12628792-12628793	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs115167269	chr7:12628807-12628808	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs568203202	chr7:12628841-12628842	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs547568076	chr7:12628886-12628887	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs536237604	chr7:12628897-12628898	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs369541552	chr7:12628922-12628923	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs371769029	chr7:12628934-12628935	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs112418075	chr7:12628942-12628943	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs549825977	chr7:12628952-12628953	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs569238178	chr7:12628958-12628959	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs1138963	chr7:12628993-12628994	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs369630797	chr7:12629006-12629007	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs568562736	chr7:12629015-12629016	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs534328721	chr7:12629018-12629019	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs368170340	chr7:12629031-12629032	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs558096262	chr7:12629041-12629042	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs185729190	chr7:12629064-12629065	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373995654	chr7:12629070-12629071	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs556596327	chr7:12629098-12629099	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs554552656	chr7:12629137-12629138	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs190205661	chr7:12629175-12629176	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182394320	chr7:12629244-12629245	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs571802573	chr7:12629261-12629262	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs186951089	chr7:12629289-12629290	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs80084699	chr7:12629297-12629298	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532995210	chr7:12629333-12629334	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12611800-12637600	Weak transcription	Colonic Mucosa	Colon
2	chr7:12619800-12630400	Weak transcription	Esophagus	oesophagus
3	chr7:12625000-12645800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr7:12625000-12652000	Weak transcription	Duodenum Mucosa	Duodenum
5	chr7:12625400-12667600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr7:12625600-12633400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr7:12626000-12628600	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr7:12626200-12637400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr7:12627400-12633400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:12627800-12628400	Flanking Active TSS	K562	blood
11	chr7:12628000-12629400	Enhancers	Placenta	Placenta
12	chr7:12628000-12635600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:12628400-12628600	Active TSS	K562	blood
14	chr7:12628600-12628800	Enhancers	Placenta Amnion	Placenta Amnion
15	chr7:12628600-12628800	Flanking Active TSS	K562	blood
16	chr7:12628800-12629200	Active TSS	K562	blood
17	chr7:12629200-12629600	Flanking Active TSS	K562	blood
18	chr7:12629400-12630200	Weak transcription	Placenta	Placenta
19	chr7:12629600-12630200	Active TSS	K562	blood
20	chr7:12630200-12630600	Flanking Active TSS	Placenta	Placenta
21	chr7:12630200-12630800	Flanking Active TSS	K562	blood
22	chr7:12630600-12631200	Active TSS	Placenta	Placenta
23	chr7:12630800-12631400	Active TSS	K562	blood
24	chr7:12631200-12632800	Transcr. at gene 5' and 3'	Placenta	Placenta
25	chr7:12631400-12632000	Flanking Active TSS	K562	blood
26	chr7:12632000-12632600	Enhancers	K562	blood
27	chr7:12632600-12632800	Flanking Active TSS	K562	blood
28	chr7:12632800-12633200	Active TSS	Placenta	Placenta
29	chr7:12632800-12633600	Active TSS	K562	blood
30	chr7:12633200-12633400	Transcr. at gene 5' and 3'	Placenta	Placenta
31	chr7:12633400-12635000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr7:12633400-12635000	ZNF genes & repeats	Placenta	Placenta
33	chr7:12633600-12634800	Flanking Active TSS	K562	blood
34	chr7:12633800-12634000	Enhancers	Esophagus	oesophagus
35	chr7:12634800-12635000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr7:12634800-12635600	Enhancers	K562	blood

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