Variant report

Variant	nsv605875
Chromosome Location	chr7:3117801-3134593
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	ATF2	chr7:3131973-3132406	GM12878	blood:	n/a	n/a
2	ATF2	chr7:3118024-3118508	GM12878	blood:	n/a	n/a
3	ATF2	chr7:3118056-3118550	GM12878	blood:	n/a	n/a
4	ATF2	chr7:3132072-3132548	GM12878	blood:	n/a	n/a
5	BATF	chr7:3118166-3118517	GM12878	blood:	n/a	n/a
6	BATF	chr7:3132066-3132400	GM12878	blood:	n/a	n/a
7	BCL11A	chr7:3118127-3118458	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:3118124-3118494	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:3118138-3118639	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:3118443-3118622	K562	blood:	n/a	n/a
11	BHLHE40	chr7:3120025-3120105	K562	blood:	n/a	n/a
12	BHLHE40	chr7:3122367-3122715	K562	blood:	n/a	chr7:3122437-3122446
13	BHLHE40	chr7:3132108-3132440	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:3126085-3126131	K562	blood:	n/a	n/a
15	CHD2	chr7:3118168-3118456	GM12878	blood:	n/a	n/a
16	CREB1	chr7:3131965-3132570	GM12878	blood:	n/a	chr7:3132241-3132254
17	CREB1	chr7:3117968-3118642	GM12878	blood:	n/a	n/a
18	CREB1	chr7:3132031-3132499	GM12878	blood:	n/a	chr7:3132241-3132254
19	CREB1	chr7:3118037-3118644	GM12878	blood:	n/a	n/a
20	CTCF	chr7:3129220-3129370	AG04450	lung:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
21	CTCF	chr7:3129240-3129390	GM12871	blood:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
22	CTCF	chr7:3132298-3132405	GM12892	blood:	n/a	chr7:3132354-3132367
23	CTCF	chr7:3129280-3129430	MCF-7	breast:	n/a	chr7:3129314-3129323 chr7:3129415-3129423
24	CTCF	chr7:3129300-3129450	AoAF	blood vessel:	n/a	chr7:3129314-3129323 chr7:3129415-3129423
25	CTCF	chr7:3132260-3132410	GM12872	blood:	n/a	chr7:3132354-3132367
26	CTCF	chr7:3129180-3129330	HAc	cerebellar:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
27	CTCF	chr7:3126840-3126990	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr7:3129058-3129597	MCF-7	breast:	n/a	chr7:3129314-3129323 chr7:3129415-3129423 chr7:3129243-3129252
29	CTCF	chr7:3129240-3129390	SAEC	small airway:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
30	CTCF	chr7:3129200-3129350	AG04449	skin:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
31	CTCF	chr7:3122650-3122799	K562	blood:	n/a	n/a
32	CTCF	chr7:3129218-3129410	GM19239	blood:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
33	CTCF	chr7:3128940-3129090	GM12870	blood:	n/a	n/a
34	CTCF	chr7:3129180-3129330	GM12865	blood:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
35	CTCF	chr7:3129220-3129370	HEK293	kidney:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
36	CTCF	chr7:3132200-3132350	GM12871	blood:	n/a	n/a
37	CTCF	chr7:3129080-3129230	GM06990	blood:	n/a	n/a
38	CTCF	chr7:3129203-3129427	GM13977	blood:	n/a	chr7:3129314-3129323 chr7:3129415-3129423 chr7:3129243-3129252
39	CTCF	chr7:3129200-3129350	AG09319	gingival:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
40	CTCF	chr7:3129220-3129370	HCPEpiC	choroid plexus:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
41	CTCF	chr7:3129038-3129452	K562	blood:	n/a	chr7:3129314-3129323 chr7:3129415-3129423 chr7:3129243-3129252
42	CTCF	chr7:3129300-3129450	K562	blood:	n/a	chr7:3129314-3129323 chr7:3129415-3129423
43	CTCF	chr7:3129156-3129441	T-47D	breast:	n/a	chr7:3129314-3129323 chr7:3129415-3129423 chr7:3129243-3129252
44	CTCF	chr7:3129460-3129610	HepG2	liver:	n/a	n/a
45	CTCF	chr7:3129200-3129350	HAc	cerebellar:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
46	CTCF	chr7:3129122-3129505	GM12878	blood:	n/a	chr7:3129314-3129323 chr7:3129415-3129423 chr7:3129243-3129252
47	CTCF	chr7:3129220-3129370	NB4	blood:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
48	CTCF	chr7:3129001-3129060	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:3129260-3129410	GM12870	blood:	n/a	chr7:3129314-3129323
50	CTCF	chr7:3129260-3129410	GM12871	blood:	n/a	chr7:3129314-3129323

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3134557-3134607	MCF-7	breast:	n/a
2	chr7:3134557-3134607	PANC-1	pancreas:	n/a
3	chr7:3134557-3134607	GM12892	blood:	n/a
4	chr7:3134592-3134642	MCF-7	breast:	n/a
5	chr7:3134592-3134642	PANC-1	pancreas:	n/a
6	chr7:3134592-3134642	HCPEpiC	choroid plexus:	n/a
7	chr7:3134557-3134607	PFSK-1	brain:	n/a
8	chr7:3127028-3127078	MCF10A-Er-Src	breast:	n/a
9	chr7:3127028-3127078	IMR90	lung:	fetal
10	chr7:3134592-3134642	CMK	blood:	n/a
11	chr7:3134557-3134607	Hela-S3	cervix:	n/a
12	chr7:3134592-3134642	HEEpiC	esophagus:	n/a
13	chr7:3134592-3134642	AoSMC	blood vessel:	n/a
14	chr7:3134592-3134642	K562	blood:	n/a
15	chr7:3134592-3134642	PFSK-1	brain:	n/a
16	chr7:3127028-3127078	ovcar-3	ovarian:	n/a
17	chr7:3127028-3127078	MCF-7	breast:	n/a
18	chr7:3127028-3127078	AG10803	skin:	n/a
19	chr7:3134557-3134607	BJ	skin:	n/a
20	chr7:3134557-3134607	Hepatocyte	liver:	n/a
21	chr7:3127028-3127078	CMK	blood:	n/a
22	chr7:3127028-3127078	Hela-S3	cervix:	n/a
23	chr7:3134592-3134642	HRE	kidney:	n/a
24	chr7:3127028-3127078	HMEC	breast:	n/a
25	chr7:3134592-3134642	NHBE	bronchial:	n/a
26	chr7:3134557-3134607	HCF	heart:	n/a
27	chr7:3127028-3127078	SK-N-MC	brain:	n/a
28	chr7:3127028-3127078	HepG2	liver:	n/a
29	chr7:3134592-3134642	T-47D	breast:	n/a
30	chr7:3134592-3134642	NT2-D1	testis:	n/a
31	chr7:3134592-3134642	HAEpiC	amniotic membrane:	n/a
32	chr7:3127028-3127078	HIPEpiC	eye:	n/a
33	chr7:3134557-3134607	BE2_C	brain:	n/a
34	chr7:3134592-3134642	BJ	skin:	n/a
35	chr7:3134557-3134607	HL-60	blood:	n/a
36	chr7:3127028-3127078	GM06990	blood:	n/a
37	chr7:3127028-3127078	A549	lung:	n/a
38	chr7:3134557-3134607	Caco-2	colon:	n/a
39	chr7:3134592-3134642	Jurkat	blood:	n/a
40	chr7:3127028-3127078	U87	brain:	n/a
41	chr7:3127028-3127078	Hepatocyte	liver:	n/a
42	chr7:3134592-3134642	ECC-1	luminal epithelium:	n/a
43	chr7:3134592-3134642	HNPCEpiC	eye:	n/a
44	chr7:3127028-3127078	HEEpiC	esophagus:	n/a
45	chr7:3127028-3127078	T-47D	breast:	n/a
46	chr7:3134592-3134642	GM06990	blood:	n/a
47	chr7:3134592-3134642	NHDF-neo	bronchial:	n/a
48	chr7:3134557-3134607	HEK293	kidney:	embryo
49	chr7:3127028-3127078	NHDF-neo	bronchial:	n/a
50	chr7:3127028-3127078	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:2926599..2927259-chr7:3129024..3129578,2	MCF-7	breast:
2	chr7:2913908..2916162-chr7:3122594..3124369,2	MCF-7	breast:
3	chr7:3114729..3116313-chr7:3116448..3118369,2	MCF-7	breast:
4	chr7:3113104..3115838-chr7:3115974..3117943,2	K562	blood:
5	chr7:3128837..3129871-chr7:3239803..3240577,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CARD11-3	chr7:3124135-3124176	l_3354_chr7:3100290-3107234_whiteBloodCell
2	lnc-CARD11-1	chr7:3125986-3126055	XLOC_006337
3	lnc-AC091801.1.1-5	chr7:3133765-3135219	XLOC_006338
4	lnc-CARD11-1	chr7:3122886-3123252	XLOC_006337
5	lnc-AC091801.1.1-5	chr7:3133765-3135219	XLOC_006338

Variant related genes	Relation type
ENSG00000228334	TF binding region
ENSG00000228334	CpG island
PLIN3	miRNA target sites

Extended variants
information (count: 939 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:939 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7801254	chr7:3117801-3117802	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75468300	chr7:3117804-3117805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185867090	chr7:3117814-3117815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536773731	chr7:3117826-3117827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561013669	chr7:3117848-3117849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530146354	chr7:3117860-3117861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11772124	chr7:3117874-3117875	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs113447979	chr7:3117875-3117876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76405830	chr7:3117877-3117878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147379727	chr7:3117881-3117882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553270038	chr7:3117927-3117928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566401624	chr7:3117941-3117942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189696237	chr7:3117951-3117952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138060512	chr7:3117953-3117954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577841716	chr7:3117977-3117978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143515571	chr7:3118006-3118007	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs180874447	chr7:3118037-3118038	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147147396	chr7:3118063-3118064	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7783136	chr7:3118073-3118074	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs375924223	chr7:3118078-3118079	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs367763197	chr7:3118084-3118085	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs557060141	chr7:3118089-3118090	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576750751	chr7:3118101-3118102	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139447657	chr7:3118115-3118116	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117581190	chr7:3118128-3118129	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564157710	chr7:3118157-3118158	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572818242	chr7:3118205-3118206	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs386709412	chr7:3118246-3118247	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555145195	chr7:3118247-3118248	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs373755829	chr7:3118255-3118256	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187266679	chr7:3118270-3118271	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543543272	chr7:3118274-3118275	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563839337	chr7:3118278-3118279	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs17132944	chr7:3118298-3118299	ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs562204131	chr7:3118300-3118301	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546239337	chr7:3118308-3118309	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs149749168	chr7:3118319-3118320	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528802219	chr7:3118323-3118324	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548948064	chr7:3118325-3118326	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529559830	chr7:3118372-3118373	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144579319	chr7:3118373-3118374	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192015263	chr7:3118380-3118381	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs73298820	chr7:3118381-3118382	ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs570549773	chr7:3118407-3118408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539013377	chr7:3118422-3118423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs199934778	chr7:3118424-3118425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552560414	chr7:3118427-3118428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566383967	chr7:3118452-3118453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs535358220	chr7:3118490-3118491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555282006	chr7:3118522-3118523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:157 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3117600-3119000	Enhancers	Primary B cells from peripheral blood	blood
2	chr7:3118000-3118400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:3118000-3118600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr7:3118400-3119000	Enhancers	GM12878-XiMat	blood
5	chr7:3118400-3122400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:3119000-3121800	Weak transcription	Primary B cells from peripheral blood	blood
7	chr7:3121600-3123600	Enhancers	Adipose Nuclei	Adipose
8	chr7:3121800-3123000	Enhancers	Primary B cells from peripheral blood	blood
9	chr7:3122000-3123600	Enhancers	Placenta	Placenta
10	chr7:3122200-3122600	Enhancers	Primary T cells fromperipheralblood	blood
11	chr7:3122200-3122800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr7:3122400-3122800	Enhancers	Primary B cells from cord blood	blood
13	chr7:3122600-3123200	Enhancers	Aorta	Aorta
14	chr7:3123000-3124200	Enhancers	Fetal Brain Male	brain
15	chr7:3123000-3130200	Weak transcription	Primary B cells from peripheral blood	blood
16	chr7:3123200-3126400	Weak transcription	Aorta	Aorta
17	chr7:3125000-3126600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:3126200-3126800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr7:3126400-3126800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr7:3126400-3127000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr7:3126400-3127000	Bivalent Enhancer	Placenta	Placenta
22	chr7:3126400-3127400	Enhancers	Aorta	Aorta
23	chr7:3126600-3126800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr7:3126600-3127400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr7:3126600-3127400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr7:3126600-3127400	Bivalent Enhancer	Fetal Stomach	stomach
27	chr7:3126600-3128000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:3126800-3127400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr7:3126800-3127600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:3126800-3127800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr7:3126800-3131000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:3127400-3128800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr7:3127800-3128000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr7:3128800-3129000	Enhancers	Esophagus	oesophagus
35	chr7:3128800-3129400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr7:3128800-3129600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:3128800-3129600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr7:3128800-3131400	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr7:3128800-3131600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr7:3128800-3131600	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr7:3128800-3132200	Enhancers	Primary T cells fromperipheralblood	blood
42	chr7:3128800-3134200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr7:3128800-3134400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr7:3129000-3131200	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr7:3129000-3131800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr7:3129000-3131800	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr7:3129200-3129400	Enhancers	Primary hematopoietic stem cells	blood
48	chr7:3129200-3129400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:3129200-3130600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
50	chr7:3129200-3131800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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