Variant report

Variant	nsv887986
Chromosome Location	chr7:40311382-40425140
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	ATF1	chr7:40386153-40386787	K562	blood:	n/a	n/a
2	ATF1	chr7:40369219-40369450	K562	blood:	n/a	n/a
3	BACH1	chr7:40424889-40425009	K562	blood:	n/a	n/a
4	BACH1	chr7:40335510-40335517	K562	blood:	n/a	n/a
5	BCL3	chr7:40396941-40397261	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:40369274-40369393	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:40371071-40371334	K562	blood:	n/a	n/a
8	CEBPB	chr7:40346853-40346935	HepG2	liver:	n/a	chr7:40346890-40346901
9	CEBPB	chr7:40352312-40352434	HepG2	liver:	n/a	chr7:40352333-40352344
10	CEBPB	chr7:40394430-40394767	IMR90	lung:	n/a	chr7:40394598-40394609
11	CEBPB	chr7:40400575-40400713	HepG2	liver:	n/a	chr7:40400597-40400608
12	CEBPB	chr7:40400524-40400714	A549	lung:	n/a	chr7:40400597-40400608
13	CEBPB	chr7:40413702-40413911	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:40386245-40386478	K562	blood:	n/a	n/a
15	CEBPB	chr7:40394474-40394666	HepG2	liver:	n/a	chr7:40394598-40394609
16	CEBPB	chr7:40400497-40400736	IMR90	lung:	n/a	chr7:40400597-40400608
17	CHD1	chr7:40369385-40369414	GM12878	blood:	n/a	n/a
18	CHD2	chr7:40386347-40386531	K562	blood:	n/a	n/a
19	CTCF	chr7:40397440-40397590	K562	blood:	n/a	n/a
20	CTCF	chr7:40368900-40369050	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr7:40368140-40368290	RPTEC	kidney:	n/a	chr7:40368187-40368208 chr7:40368192-40368210
22	CTCF	chr7:40335720-40335870	K562	blood:	n/a	n/a
23	CTCF	chr7:40369230-40369445	GM13977	blood:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
24	CTCF	chr7:40369162-40369649	HCT-116	colon:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
25	CTCF	chr7:40335900-40336050	HRE	kidney:	n/a	n/a
26	CTCF	chr7:40397400-40397550	HMF	breast:	n/a	n/a
27	CTCF	chr7:40368980-40369130	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr7:40378307-40378328	GM13976	blood:	n/a	n/a
29	CTCF	chr7:40369300-40369450	BE2_C	brain:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
30	CTCF	chr7:40369300-40369450	RPTEC	kidney:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
31	CTCF	chr7:40369260-40369410	HCM	heart:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
32	CTCF	chr7:40335840-40335990	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr7:40348256-40348290	GM20000	blood:	n/a	n/a
34	CTCF	chr7:40371120-40371270	BE2_C	brain:	n/a	n/a
35	CTCF	chr7:40369260-40369410	HMF	breast:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
36	CTCF	chr7:40369160-40369506	K562	blood:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
37	CTCF	chr7:40369213-40369485	K562	blood:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
38	CTCF	chr7:40369240-40369390	GM12864	blood:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
39	CTCF	chr7:40369230-40369464	Pancreas_OC	pancreas:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
40	CTCF	chr7:40369260-40369410	K562	blood:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
41	CTCF	chr7:40369300-40369450	NHLF	lung:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
42	CTCF	chr7:40335860-40336010	AG04449	skin:	n/a	n/a
43	CTCF	chr7:40369280-40369430	HPAF	blood vessel:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
44	CTCF	chr7:40360272-40360323	Hela-S3	cervix:	n/a	chr7:40360279-40360300
45	CTCF	chr7:40335793-40336116	K562	blood:	n/a	n/a
46	CTCF	chr7:40369128-40369601	IMR90	lung:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
47	CTCF	chr7:40371200-40371350	BE2_C	brain:	n/a	n/a
48	CTCF	chr7:40397400-40397550	RPTEC	kidney:	n/a	n/a
49	CTCF	chr7:40368980-40369130	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr7:40335820-40335970	HAc	cerebellar:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:40338163-40338213	RPTEC	kidney:	n/a
2	chr7:40367873-40367923	HRPEpiC	eye:	n/a
3	chr7:40367873-40367923	HPAEpiC	pulmonary alveolar:	n/a
4	chr7:40367873-40367923	HepG2	liver:	n/a
5	chr7:40367873-40367923	HL-60	blood:	n/a
6	chr7:40338163-40338213	AG09319	gingival:	n/a
7	chr7:40367873-40367923	AoSMC	blood vessel:	n/a
8	chr7:40367873-40367923	HCT-116	colon:	n/a
9	chr7:40338163-40338213	HCM	heart:	n/a
10	chr7:40338163-40338213	NT2-D1	testis:	n/a
11	chr7:40367873-40367923	K562	blood:	n/a
12	chr7:40338163-40338213	Hela-S3	cervix:	n/a
13	chr7:40338163-40338213	HEK293	kidney:	embryo
14	chr7:40338163-40338213	SAEC	small airway:	n/a
15	chr7:40338163-40338213	SK-N-MC	brain:	n/a
16	chr7:40338163-40338213	HCPEpiC	choroid plexus:	n/a
17	chr7:40367873-40367923	AG10803	skin:	n/a
18	chr7:40338163-40338213	MCF10A-Er-Src	breast:	n/a
19	chr7:40338163-40338213	HUVEC	blood vessel:	n/a
20	chr7:40367873-40367923	Hepatocyte	liver:	n/a
21	chr7:40367873-40367923	IMR90	lung:	fetal
22	chr7:40367873-40367923	NB4	blood:	n/a
23	chr7:40338163-40338213	HMEC	breast:	n/a
24	chr7:40338163-40338213	CMK	blood:	n/a
25	chr7:40367873-40367923	HAEpiC	amniotic membrane:	n/a
26	chr7:40367873-40367923	AG09309	skin:	n/a
27	chr7:40338163-40338213	GM19239	blood:	n/a
28	chr7:40338163-40338213	ovcar-3	ovarian:	n/a
29	chr7:40338163-40338213	Caco-2	colon:	n/a
30	chr7:40338163-40338213	MCF-7	breast:	n/a
31	chr7:40338163-40338213	HCF	heart:	n/a
32	chr7:40367873-40367923	SAEC	small airway:	n/a
33	chr7:40367873-40367923	HCM	heart:	n/a
34	chr7:40338163-40338213	HRCEpiC	kidney:	n/a
35	chr7:40367873-40367923	NHDF-neo	bronchial:	n/a
36	chr7:40367873-40367923	HEEpiC	esophagus:	n/a
37	chr7:40338163-40338213	SK-N-SH	brain:	n/a
38	chr7:40338163-40338213	HL-60	blood:	n/a
39	chr7:40338163-40338213	PrEC	prostate:	n/a
40	chr7:40338163-40338213	AG10803	skin:	n/a
41	chr7:40338163-40338213	HRPEpiC	eye:	n/a
42	chr7:40338163-40338213	HAEpiC	amniotic membrane:	n/a
43	chr7:40338163-40338213	IMR90	lung:	fetal
44	chr7:40338163-40338213	AG04449	skin:	fetal
45	chr7:40367873-40367923	HNPCEpiC	eye:	n/a
46	chr7:40338163-40338213	HPAEpiC	pulmonary alveolar:	n/a
47	chr7:40367873-40367923	HEK293	kidney:	embryo
48	chr7:40367873-40367923	RPTEC	kidney:	n/a
49	chr7:40338163-40338213	HCT-116	colon:	n/a
50	chr7:40367873-40367923	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:40344397..40346549-chr7:40349560..40351479,2	K562	blood:
2	chr7:40345049..40347172-chr7:40349979..40352115,2	K562	blood:
3	chr7:40344397..40346549-chr7:40349560..40351479,2	K562	blood:
4	chr7:40334583..40336119-chr7:40353617..40356349,2	K562	blood:
5	chr1:6483244..6484243-chr7:40333894..40334600,2	MCF-7	breast:
6	chr7:40362786..40364533-chr7:40364996..40369227,3	K562	blood:
7	chr7:40334583..40336119-chr7:40353617..40356349,2	K562	blood:
8	chr7:39988445..39991258-chr7:40413776..40416750,2	K562	blood:
9	chr7:40348620..40350328-chr7:40353767..40356702,2	K562	blood:
10	chr7:40348620..40350328-chr7:40353767..40356702,2	K562	blood:
11	chr7:40345049..40347172-chr7:40349979..40352115,2	K562	blood:
12	chr7:40362786..40364533-chr7:40364996..40369227,3	K562	blood:
13	chr7:40368904..40369830-chr7:40644119..40645087,4	MCF-7	breast:
14	chr20:57473196..57474009-chr7:40413360..40414065,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf11-8	chr7:40336722-40336813	NONHSAT120249
2	lnc-C7orf11-8	chr7:40333941-40333997	NONHSAT120249

Variant related genes	Relation type
SUGCT	TF binding region
SUGCT	CpG island
ENSG00000065883	chromatin interactions
ENSG00000259826	chromatin interactions

Extended variants
information (count: 3552 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3552 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10234315	chr7:40311382-40311383	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561564043	chr7:40311392-40311393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78466990	chr7:40311415-40311416	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs534737852	chr7:40311456-40311457	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs370199738	chr7:40311472-40311473	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs558118713	chr7:40311553-40311554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577876351	chr7:40311565-40311566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73133536	chr7:40311577-40311578	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs557195726	chr7:40311599-40311600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375283858	chr7:40311668-40311669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182101253	chr7:40311690-40311691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571852240	chr7:40311691-40311692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs55872099	chr7:40311692-40311693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs11973386	chr7:40311694-40311695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs193218682	chr7:40311696-40311697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201050391	chr7:40311698-40311699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs59953340	chr7:40311711-40311712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6979211	chr7:40311712-40311713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368627404	chr7:40311741-40311742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528165019	chr7:40311784-40311785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184012617	chr7:40311790-40311791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567563859	chr7:40311792-40311793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs58480323	chr7:40311793-40311794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73318545	chr7:40311835-40311836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73318549	chr7:40311862-40311863	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs145957114	chr7:40311887-40311888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372632544	chr7:40311890-40311891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139815331	chr7:40311934-40311935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549533900	chr7:40311936-40311937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566075626	chr7:40311937-40311938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79560080	chr7:40311950-40311951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192261515	chr7:40312036-40312037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183980237	chr7:40312069-40312070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555112854	chr7:40312087-40312088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377258538	chr7:40312109-40312110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537350819	chr7:40312132-40312133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs57941896	chr7:40312142-40312143	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs536379162	chr7:40312180-40312181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12538240	chr7:40312205-40312206	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs200726368	chr7:40312257-40312258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201968545	chr7:40312260-40312261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs58906847	chr7:40312263-40312264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200348045	chr7:40312264-40312265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201517386	chr7:40312265-40312266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12535794	chr7:40312266-40312267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572866075	chr7:40312269-40312270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533992175	chr7:40312344-40312345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149952487	chr7:40312351-40312352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs578021901	chr7:40312352-40312353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530465570	chr7:40312354-40312355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	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
Autism	22495311	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:363 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:40304400-40323600	Weak transcription	HepG2	liver
2	chr7:40312000-40337000	Weak transcription	HSMM	muscle
3	chr7:40313200-40313600	Enhancers	Adipose Nuclei	Adipose
4	chr7:40313600-40319800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:40316200-40316400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr7:40316400-40316600	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr7:40316600-40318800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr7:40317400-40344600	Weak transcription	Aorta	Aorta
9	chr7:40318800-40320600	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr7:40319600-40320000	Enhancers	Dnd41	blood
11	chr7:40319800-40320000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr7:40322400-40323200	Enhancers	Liver	Liver
13	chr7:40322800-40326800	Weak transcription	Ovary	ovary
14	chr7:40323600-40323800	Enhancers	HepG2	liver
15	chr7:40326400-40326800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr7:40331400-40332600	Enhancers	Dnd41	blood
17	chr7:40331600-40332400	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr7:40332400-40337600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr7:40332600-40337400	Weak transcription	Dnd41	blood
20	chr7:40335400-40339200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr7:40335600-40335800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr7:40335600-40337800	Enhancers	Muscle Satellite Cultured Cells	--
23	chr7:40335800-40341400	Enhancers	HUVEC	blood vessel
24	chr7:40336000-40339200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr7:40336000-40340200	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr7:40336200-40340600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr7:40336400-40336600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr7:40336600-40339000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr7:40336800-40338600	Enhancers	Osteobl	bone
30	chr7:40336800-40339200	Enhancers	HSMMtube	muscle
31	chr7:40336800-40342000	Enhancers	NH-A	brain
32	chr7:40336800-40342600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr7:40337000-40337800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr7:40337000-40339200	Enhancers	NHEK	skin
35	chr7:40337000-40341400	Enhancers	HMEC	breast
36	chr7:40337000-40341800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr7:40337000-40342600	Enhancers	HSMM	muscle
38	chr7:40337200-40337800	Enhancers	NHLF	lung
39	chr7:40337200-40338000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:40337200-40339400	Enhancers	NHDF-Ad	bronchial
41	chr7:40337400-40341400	Enhancers	Dnd41	blood
42	chr7:40337600-40338800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr7:40337600-40339000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr7:40337600-40339200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr7:40337600-40339200	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr7:40337600-40339200	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr7:40337600-40339400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr7:40337800-40338200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr7:40337800-40338600	Weak transcription	NHLF	lung
50	chr7:40337800-40338800	Flanking Active TSS	Muscle Satellite Cultured Cells	--

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