Variant report

Variant	nsv887712
Chromosome Location	chr7:14717872-14829858
allele	n/a
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	ARID3A	chr7:14731292-14731525	HepG2	liver:	n/a	n/a
2	BACH1	chr7:14801803-14801897	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr7:14753814-14754199	GM12878	blood:	n/a	n/a
4	BATF	chr7:14753768-14754244	GM12878	blood:	n/a	n/a
5	BCL11A	chr7:14753850-14754156	GM12878	blood:	n/a	n/a
6	BCL11A	chr7:14753810-14754239	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:14753608-14754277	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:14726975-14727218	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:14755029-14755228	GM12878	blood:	n/a	n/a
10	BRCA1	chr7:14764275-14764309	GM12878	blood:	n/a	n/a
11	CBX3	chr7:14788013-14788469	HCT-116	colon:	n/a	n/a
12	CBX3	chr7:14780242-14780709	HCT-116	colon:	n/a	n/a
13	CCNT2	chr7:14733536-14733651	K562	blood:	n/a	n/a
14	CEBPB	chr7:14763021-14763046	A549	lung:	n/a	n/a
15	CEBPB	chr7:14817839-14817999	HepG2	liver:	n/a	chr7:14817887-14817898
16	CEBPB	chr7:14798805-14799120	A549	lung:	n/a	chr7:14798950-14798961
17	CEBPB	chr7:14732871-14732955	A549	lung:	n/a	chr7:14732893-14732906 chr7:14732893-14732906 chr7:14732893-14732904 chr7:14732895-14732906
18	CEBPB	chr7:14798836-14799033	H1-hESC	embryonic stem cell:	n/a	chr7:14798950-14798961
19	CEBPB	chr7:14722870-14723114	HepG2	liver:	n/a	chr7:14722949-14722962 chr7:14722949-14722960
20	CEBPB	chr7:14732786-14733038	HepG2	liver:	n/a	chr7:14732893-14732906 chr7:14732893-14732906 chr7:14732893-14732904 chr7:14732895-14732906
21	CEBPB	chr7:14791139-14791343	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:14798864-14799064	K562	blood:	n/a	chr7:14798950-14798961
23	CEBPB	chr7:14798788-14799108	HepG2	liver:	n/a	chr7:14798950-14798961
24	CEBPB	chr7:14779288-14779508	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:14732861-14732918	K562	blood:	n/a	chr7:14732893-14732906 chr7:14732893-14732906 chr7:14732893-14732904 chr7:14732895-14732906
26	CEBPB	chr7:14779216-14779543	Hela-S3	cervix:	n/a	n/a
27	CHD1	chr7:14755305-14755322	GM12878	blood:	n/a	n/a
28	CHD1	chr7:14757621-14757790	GM12878	blood:	n/a	n/a
29	CHD1	chr7:14774946-14774959	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr7:14753760-14754087	GM12878	blood:	n/a	n/a
31	CHD2	chr7:14753745-14754304	GM12878	blood:	n/a	n/a
32	CTCF	chr7:14757520-14757670	GM12872	blood:	n/a	chr7:14757524-14757542
33	CTCF	chr7:14774500-14774650	GM12878	blood:	n/a	n/a
34	CTCF	chr7:14757440-14757590	GM06990	blood:	n/a	chr7:14757524-14757542
35	CTCF	chr7:14731323-14731575	GM12878	blood:	n/a	chr7:14731434-14731450 chr7:14731428-14731449 chr7:14731433-14731451
36	CTCF	chr7:14731380-14731530	RPTEC	kidney:	n/a	chr7:14731434-14731450 chr7:14731428-14731449 chr7:14731433-14731451
37	CTCF	chr7:14774509-14774608	NHEK	skin:	n/a	n/a
38	CTCF	chr7:14757453-14757619	Kidney_OC	kidney:	n/a	chr7:14757524-14757542
39	CTCF	chr7:14731400-14731550	HL-60	blood:	n/a	chr7:14731434-14731450 chr7:14731428-14731449 chr7:14731433-14731451
40	CTCF	chr7:14737960-14738110	BE2_C	brain:	n/a	chr7:14738016-14738037 chr7:14738017-14738030 chr7:14738014-14738032 chr7:14738015-14738031
41	CTCF	chr7:14774460-14774610	GM12874	blood:	n/a	n/a
42	CTCF	chr7:14757480-14757630	AG09319	gingival:	n/a	chr7:14757524-14757542
43	CTCF	chr7:14731380-14731530	HMF	breast:	n/a	chr7:14731434-14731450 chr7:14731428-14731449 chr7:14731433-14731451
44	CTCF	chr7:14774420-14774570	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr7:14731400-14731550	GM12873	blood:	n/a	chr7:14731434-14731450 chr7:14731428-14731449 chr7:14731433-14731451
46	CTCF	chr7:14774439-14774622	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr7:14731220-14731370	WI-38	lung:	n/a	n/a
48	CTCF	chr7:14774480-14774630	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr7:14757398-14757674	Medullo	brain:	n/a	chr7:14757524-14757542
50	CTCF	chr7:14737842-14738247	GM12878	blood:	n/a	chr7:14738016-14738037 chr7:14738017-14738030 chr7:14738014-14738032 chr7:14738015-14738031

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:14755869-14755919	MCF10A-Er-Src	breast:	n/a
2	chr7:14755869-14755919	MCF10A-Er-Src	breast:	n/a
3	chr7:14755869-14755919	AoSMC	blood vessel:	n/a
4	chr7:14755869-14755919	IMR90	lung:	fetal
5	chr7:14755869-14755919	SK-N-SH_RA	brain:	n/a
6	chr7:14755869-14755919	AG09319	gingival:	n/a
7	chr7:14809526-14809576	GM06990	blood:	n/a
8	chr7:14801527-14801577	HRCEpiC	kidney:	n/a
9	chr7:14801527-14801577	AG10803	skin:	n/a
10	chr7:14801527-14801577	HRPEpiC	eye:	n/a
11	chr7:14755869-14755919	GM19239	blood:	n/a
12	chr7:14755869-14755919	H1-hESC	embryonic stem cell:	embryo
13	chr7:14755869-14755919	T-47D	breast:	n/a
14	chr7:14755869-14755919	NT2-D1	testis:	n/a
15	chr7:14801527-14801577	AG09309	skin:	n/a
16	chr7:14801527-14801577	Caco-2	colon:	n/a
17	chr7:14755869-14755919	LNCaP	prostate:	n/a
18	chr7:14809526-14809576	HCM	heart:	n/a
19	chr7:14809526-14809576	SK-N-SH_RA	brain:	n/a
20	chr7:14801527-14801577	AG09319	gingival:	n/a
21	chr7:14801527-14801577	HEK293	kidney:	embryo
22	chr7:14809526-14809576	Hepatocyte	liver:	n/a
23	chr7:14755869-14755919	HepG2	liver:	n/a
24	chr7:14809526-14809576	HCT-116	colon:	n/a
25	chr7:14809526-14809576	U87	brain:	n/a
26	chr7:14755869-14755919	NHBE	bronchial:	n/a
27	chr7:14801527-14801577	NHBE	bronchial:	n/a
28	chr7:14809526-14809576	MCF-7	breast:	n/a
29	chr7:14801527-14801577	HIPEpiC	eye:	n/a
30	chr7:14809526-14809576	ovcar-3	ovarian:	n/a
31	chr7:14755869-14755919	Hela-S3	cervix:	n/a
32	chr7:14801527-14801577	NB4	blood:	n/a
33	chr7:14755869-14755919	AG04450	lung:	fetal
34	chr7:14755869-14755919	GM12892	blood:	n/a
35	chr7:14755869-14755919	HNPCEpiC	eye:	n/a
36	chr7:14755869-14755919	HCT-116	colon:	n/a
37	chr7:14801527-14801577	NH-A	brain:	n/a
38	chr7:14809526-14809576	HMEC	breast:	n/a
39	chr7:14755869-14755919	HRE	kidney:	n/a
40	chr7:14801527-14801577	HepG2	liver:	n/a
41	chr7:14801527-14801577	HNPCEpiC	eye:	n/a
42	chr7:14809526-14809576	IMR90	lung:	fetal
43	chr7:14755869-14755919	HUVEC	blood vessel:	n/a
44	chr7:14809526-14809576	HEEpiC	esophagus:	n/a
45	chr7:14809526-14809576	AG09309	skin:	n/a
46	chr7:14755869-14755919	NB4	blood:	n/a
47	chr7:14755869-14755919	U87	brain:	n/a
48	chr7:14801527-14801577	Jurkat	blood:	n/a
49	chr7:14801527-14801577	K562	blood:	n/a
50	chr7:14801527-14801577	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:14757340..14758014-chr7:15344576..15345303,4	MCF-7	breast:
2	chr7:14757081..14758001-chr7:15054605..15056087,5	MCF-7	breast:
3	chr7:14757083..14757697-chr7:15760291..15761216,2	MCF-7	breast:
4	chr7:14756304..14757028-chr7:15055834..15056611,2	MCF-7	breast:
5	chr7:13306388..13306972-chr7:14730968..14731509,2	K562	blood:
6	chr19:16666192..16668133-chr7:14727799..14729299,2	MCF-7	breast:
7	chr19:46171433..46173080-chr7:14824864..14826364,2	K562	blood:
8	chr7:13322023..13322580-chr7:14731384..14731908,2	MCF-7	breast:
9	chr7:13319194..13320144-chr7:14730989..14732251,8	K562	blood:
10	chr7:14757467..14758291-chr7:15055705..15056411,2	MCF-7	breast:
11	chr2:169630126..169630739-chr7:14783533..14784033,2	MCF-7	breast:
12	chr7:13321688..13322613-chr7:14730587..14732153,8	MCF-7	breast:
13	chr7:14737644..14738448-chr7:15055761..15056392,2	MCF-7	breast:
14	chr7:13319140..13319925-chr7:14729283..14730100,2	K562	blood:

Variant related genes	Relation type
DGKB	TF binding region
ENSG00000221428	TF binding region
DGKB	CpG island
ENSG00000221428	CpG island
ENSG00000010310	chromatin interactions
ENSG00000127526	chromatin interactions

Extended variants
information (count: 4410 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4410 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6956435	chr7:14717872-14717873	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs181435321	chr7:14717905-14717906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532406290	chr7:14717921-14717922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186966762	chr7:14717951-14717952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6956606	chr7:14717964-14717965	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs144911865	chr7:14717982-14717983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149058056	chr7:14717994-14717995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568109060	chr7:14718037-14718038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533654946	chr7:14718040-14718041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs375732590	chr7:14718074-14718075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576780128	chr7:14718083-14718084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs539475403	chr7:14718084-14718085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559270233	chr7:14718091-14718092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576054313	chr7:14718094-14718095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190112364	chr7:14718124-14718125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182328111	chr7:14718131-14718132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574825995	chr7:14718150-14718151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142134701	chr7:14718156-14718157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146697599	chr7:14718160-14718161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531930136	chr7:14718163-14718164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532382302	chr7:14718236-14718237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186339544	chr7:14718238-14718239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562435823	chr7:14718247-14718248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545602688	chr7:14718298-14718299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531513582	chr7:14718312-14718313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547934779	chr7:14718384-14718385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568183632	chr7:14718391-14718392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs527348144	chr7:14718444-14718445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs113295567	chr7:14718451-14718452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570554021	chr7:14718474-14718475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs74985732	chr7:14718495-14718496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs373454464	chr7:14718507-14718508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73680176	chr7:14718552-14718553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569530504	chr7:14718558-14718559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140316552	chr7:14718592-14718593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555113704	chr7:14718609-14718610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574947693	chr7:14718637-14718638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs202170219	chr7:14718667-14718668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs145472338	chr7:14718692-14718693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553974346	chr7:14718702-14718703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563936497	chr7:14718704-14718705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576966135	chr7:14718742-14718743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376434541	chr7:14718750-14718751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545754080	chr7:14718779-14718780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138093218	chr7:14718783-14718784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531474970	chr7:14718788-14718789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564501396	chr7:14718810-14718811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs200367367	chr7:14718811-14718812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183263080	chr7:14718812-14718813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201332773	chr7:14718842-14718843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	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
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Colorectal cancer	21645411	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:370 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14704200-14736000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr7:14712800-14775200	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr7:14717800-14719000	Enhancers	Fetal Heart	heart
4	chr7:14720400-14723600	Weak transcription	Brain Anterior Caudate	brain
5	chr7:14720800-14728400	Weak transcription	Brain Angular Gyrus	brain
6	chr7:14722000-14722400	Active TSS	Brain Substantia Nigra	brain
7	chr7:14722200-14722400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:14722400-14723000	Weak transcription	Brain Substantia Nigra	brain
9	chr7:14722400-14724800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:14722400-14726800	Weak transcription	Osteobl	bone
11	chr7:14724800-14725000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:14724800-14725000	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr7:14724800-14725200	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr7:14724800-14725400	Enhancers	Fetal Muscle Leg	muscle
15	chr7:14725000-14725200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:14725000-14725200	Bivalent Enhancer	HSMMtube	muscle
17	chr7:14725000-14725400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr7:14725200-14725400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:14725400-14725600	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr7:14725400-14727400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr7:14725600-14727600	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr7:14726600-14727000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr7:14726800-14728200	Enhancers	Osteobl	bone
24	chr7:14727200-14727800	Enhancers	HUVEC	blood vessel
25	chr7:14727400-14727800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr7:14727400-14728000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr7:14727400-14728000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr7:14727400-14728400	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr7:14727400-14728400	Enhancers	Liver	Liver
30	chr7:14727600-14727800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr7:14727600-14727800	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr7:14727600-14728400	Enhancers	Fetal Lung	lung
33	chr7:14727800-14728000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr7:14727800-14728200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
35	chr7:14727800-14728600	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr7:14728000-14728200	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr7:14728000-14728400	Enhancers	Fetal Kidney	kidney
38	chr7:14728000-14729200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr7:14728200-14729200	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr7:14728200-14729400	Weak transcription	Osteobl	bone
41	chr7:14728400-14728800	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr7:14728400-14729400	Weak transcription	Liver	Liver
43	chr7:14728400-14729600	Weak transcription	Fetal Kidney	kidney
44	chr7:14728400-14729600	Weak transcription	Fetal Lung	lung
45	chr7:14728600-14729000	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr7:14728800-14731400	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr7:14729000-14729800	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr7:14729200-14729400	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr7:14729400-14729600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr7:14729400-14729600	Enhancers	Liver	Liver

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