Variant report

Variant	esv1813996
Chromosome Location	chr7:149730512-149750091
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:333)
CpG islands
(count:1343)
Chromatin interactive
region (count:1)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:149742080-149742094	K562	blood:	n/a	n/a
2	BACH1	chr7:149746378-149746646	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr7:149743485-149743750	GM12878	blood:	n/a	n/a
4	CHD1	chr7:149746398-149746684	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr7:149746382-149746488	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr7:149742751-149742960	GM12878	blood:	n/a	n/a
7	CTCF	chr7:149746100-149746337	K562	blood:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
8	CTCF	chr7:149742836-149742991	GM13977	blood:	n/a	n/a
9	CTCF	chr7:149742780-149742930	HCFaa	heart:	n/a	n/a
10	CTCF	chr7:149742800-149742950	HMEC	breast:	n/a	n/a
11	CTCF	chr7:149746049-149746383	MCF-7	breast:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
12	CTCF	chr7:149746051-149746369	GM12891	blood:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
13	CTCF	chr7:149742787-149743045	K562	blood:	n/a	n/a
14	CTCF	chr7:149742800-149742950	HL-60	blood:	n/a	n/a
15	CTCF	chr7:149742755-149743007	IMR90	lung:	n/a	n/a
16	CTCF	chr7:149744020-149744170	HRPEpiC	eye:	n/a	n/a
17	CTCF	chr7:149745920-149746070	SAEC	small airway:	n/a	n/a
18	CTCF	chr7:149742800-149742973	GM10248	blood:	n/a	n/a
19	CTCF	chr7:149742835-149743104	GM10266	blood:	n/a	n/a
20	CTCF	chr7:149745900-149746050	HEK293	kidney:	n/a	n/a
21	CTCF	chr7:149742852-149742998	GM13976	blood:	n/a	n/a
22	CTCF	chr7:149742820-149742970	HRPEpiC	eye:	n/a	n/a
23	CTCF	chr7:149746045-149746331	A549	lung:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
24	CTCF	chr7:149742680-149742830	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr7:149742820-149742970	HAc	cerebellar:	n/a	n/a
26	CTCF	chr7:149742820-149742970	HCT-116	colon:	n/a	n/a
27	CTCF	chr7:149746300-149746450	Caco-2	colon:	n/a	n/a
28	CTCF	chr7:149742700-149742850	GM06990	blood:	n/a	n/a
29	CTCF	chr7:149746059-149746375	MCF-7	breast:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
30	CTCF	chr7:149742840-149742990	A549	lung:	n/a	n/a
31	CTCF	chr7:149745920-149746070	HepG2	liver:	n/a	n/a
32	CTCF	chr7:149742840-149742990	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr7:149742779-149743012	A549	lung:	n/a	n/a
34	CTCF	chr7:149745619-149745710	H1-hESC	embryonic stem cell:	n/a	chr7:149745696-149745706
35	CTCF	chr7:149742800-149742950	HVMF	connective:	n/a	n/a
36	CTCF	chr7:149746200-149746350	HL-60	blood:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
37	CTCF	chr7:149742780-149742930	AG09309	skin:	n/a	n/a
38	CTCF	chr7:149746074-149746318	LNCaP	prostate:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
39	CTCF	chr7:149742881-149742934	Lung_OC	lung:	n/a	n/a
40	CTCF	chr7:149746320-149746470	NHEK	skin:	n/a	n/a
41	CTCF	chr7:149746099-149746337	A549	lung:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
42	CTCF	chr7:149742700-149742850	BE2_C	brain:	n/a	n/a
43	CTCF	chr7:149745920-149746070	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:149742680-149742970	NHLF	lung:	n/a	n/a
45	CTCF	chr7:149742800-149742950	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr7:149743099-149743204	LNCaP	prostate:	n/a	n/a
47	CTCF	chr7:149749335-149749412	HepG2	liver:	n/a	chr7:149749391-149749400
48	CTCF	chr7:149742800-149742950	HCT-116	colon:	n/a	n/a
49	CTCF	chr7:149743124-149743217	LNCaP	prostate:	n/a	n/a
50	CTCF	chr7:149746126-149746317	HepG2	liver:	n/a	chr7:149746208-149746221 chr7:149746248-149746261

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:149744597-149744647	PANC-1	pancreas:	n/a
2	chr7:149744597-149744647	PANC-1	pancreas:	n/a
3	chr7:149746468-149746518	NB4	blood:	n/a
4	chr7:149744935-149744985	GM12892	blood:	n/a
5	chr7:149746640-149746690	AG09309	skin:	n/a
6	chr7:149749941-149749991	AG10803	skin:	n/a
7	chr7:149744597-149744647	GM12891	blood:	n/a
8	chr7:149744935-149744985	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:149744041-149744091	Hepatocyte	liver:	n/a
10	chr7:149731767-149731817	NB4	blood:	n/a
11	chr7:149746468-149746518	CMK	blood:	n/a
12	chr7:149745299-149745349	SK-N-SH_RA	brain:	n/a
13	chr7:149746077-149746127	T-47D	breast:	n/a
14	chr7:149735726-149735776	Jurkat	blood:	n/a
15	chr7:149733821-149733871	AG09319	gingival:	n/a
16	chr7:149746077-149746127	GM12878	blood:	n/a
17	chr7:149742121-149742171	SK-N-SH	brain:	n/a
18	chr7:149744418-149744468	HCM	heart:	n/a
19	chr7:149746468-149746518	HIPEpiC	eye:	n/a
20	chr7:149746468-149746518	AG04449	skin:	fetal
21	chr7:149736127-149736177	AG04450	lung:	fetal
22	chr7:149733103-149733153	HMEC	breast:	n/a
23	chr7:149736127-149736177	SK-N-SH	brain:	n/a
24	chr7:149746077-149746127	AG10803	skin:	n/a
25	chr7:149732847-149732897	BE2_C	brain:	n/a
26	chr7:149738473-149738523	GM06990	blood:	n/a
27	chr7:149744418-149744468	AoSMC	blood vessel:	n/a
28	chr7:149735729-149735779	HRCEpiC	kidney:	n/a
29	chr7:149733821-149733871	GM19239	blood:	n/a
30	chr7:149733821-149733871	HEK293	kidney:	embryo
31	chr7:149732579-149732629	MCF10A-Er-Src	breast:	n/a
32	chr7:149746077-149746127	NB4	blood:	n/a
33	chr7:149738473-149738523	SKMC	muscle:	n/a
34	chr7:149746468-149746518	LNCaP	prostate:	n/a
35	chr7:149734481-149734531	H1-hESC	embryonic stem cell:	embryo
36	chr7:149731742-149731792	HCT-116	colon:	n/a
37	chr7:149736127-149736177	HCT-116	colon:	n/a
38	chr7:149732579-149732629	HRE	kidney:	n/a
39	chr7:149735729-149735779	SAEC	small airway:	n/a
40	chr7:149733103-149733153	PANC-1	pancreas:	n/a
41	chr7:149745299-149745349	HMEC	breast:	n/a
42	chr7:149733821-149733871	BE2_C	brain:	n/a
43	chr7:149734481-149734531	A549	lung:	n/a
44	chr7:149738473-149738523	NHDF-neo	bronchial:	n/a
45	chr7:149744935-149744985	NHBE	bronchial:	n/a
46	chr7:149746468-149746518	U87	brain:	n/a
47	chr7:149735729-149735779	A549	lung:	n/a
48	chr7:149746640-149746690	AoSMC	blood vessel:	n/a
49	chr7:149731767-149731817	AG09319	gingival:	n/a
50	chr7:149735729-149735779	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:149580322..149580844-chr7:149745955..149746566,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V0E2-2	chr7:149732185-149732207	NONHSAT124087
2	lnc-ATP6V0E2-2	chr7:149737610-149737743	ENSG00000241449
3	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124088
4	lnc-ATP6V0E2-2	chr7:149738452-149738550	ENSG00000241449
5	lnc-ATP6V0E2-2	chr7:149737556-149737743	NONHSAT124091
6	lnc-ATP6V0E2-2	chr7:149738452-149738550	NONHSAT124091
7	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124087
8	lnc-ATP6V0E2-2	chr7:149735636-149735802	NONHSAT124088
9	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124091

No data

Variant related genes	Relation type
ENSG00000241449	TF binding region
ENSG00000241449	CpG island

Extended variants
information (count: 1521 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1521 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559773947	chr7:149730534-149730535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs371361883	chr7:149730540-149730541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374799387	chr7:149730543-149730544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138769255	chr7:149730547-149730548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551412175	chr7:149730550-149730551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531819580	chr7:149730551-149730552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530624217	chr7:149730555-149730556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7808224	chr7:149730558-149730559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200142065	chr7:149730593-149730594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143208622	chr7:149730624-149730625	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs2626810	chr7:149730627-149730628	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532462852	chr7:149730632-149730633	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566671495	chr7:149730638-149730639	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538520674	chr7:149730663-149730664	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148705018	chr7:149730682-149730683	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577576980	chr7:149730699-149730700	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371834002	chr7:149730704-149730705	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375221415	chr7:149730705-149730706	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35364549	chr7:149730715-149730716	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369788708	chr7:149730720-149730721	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117191732	chr7:149730734-149730735	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543552501	chr7:149730739-149730740	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557032070	chr7:149730740-149730741	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574204775	chr7:149730742-149730743	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs180736854	chr7:149730745-149730746	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559863157	chr7:149730746-149730747	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370654353	chr7:149730751-149730752	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565989424	chr7:149730765-149730766	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528802803	chr7:149730771-149730772	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375840944	chr7:149730778-149730779	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368854190	chr7:149730779-149730780	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185888840	chr7:149730781-149730782	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545668762	chr7:149730792-149730793	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564881348	chr7:149730795-149730796	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190035994	chr7:149730798-149730799	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373095968	chr7:149730801-149730802	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376391144	chr7:149730816-149730817	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530506971	chr7:149730820-149730821	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550739767	chr7:149730832-149730833	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567225581	chr7:149730840-149730841	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529763972	chr7:149730842-149730843	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113990567	chr7:149730844-149730845	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370819250	chr7:149730850-149730851	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112675258	chr7:149730853-149730854	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566617601	chr7:149730854-149730855	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs202188388	chr7:149730857-149730858	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538557647	chr7:149730865-149730866	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201763252	chr7:149730885-149730886	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552045465	chr7:149730888-149730889	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549332342	chr7:149730901-149730902	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:149729600-149730600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:149730200-149744000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr7:149730600-149731000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:149733000-149744000	Weak transcription	Right Atrium	heart
5	chr7:149737000-149737200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr7:149741800-149742000	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr7:149742200-149742400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr7:149742200-149742600	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr7:149742600-149743000	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr7:149743000-149743200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
11	chr7:149743000-149743200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
12	chr7:149743000-149743200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr7:149743000-149743200	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr7:149743200-149744000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr7:149743200-149744000	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr7:149743400-149743600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
17	chr7:149743400-149743600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:149743400-149744800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
19	chr7:149743400-149745200	Weak transcription	Colon Smooth Muscle	Colon
20	chr7:149743600-149743800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
21	chr7:149743600-149744000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
22	chr7:149743800-149744000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
23	chr7:149743800-149744400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:149743800-149746600	Active TSS	Brain Anterior Caudate	brain
25	chr7:149744000-149744200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr7:149744000-149744200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:149744000-149744200	Active TSS	Cortex derived primary cultured neurospheres	brain
28	chr7:149744000-149744200	Enhancers	Fetal Brain Male	brain
29	chr7:149744000-149744400	Active TSS	Brain Germinal Matrix	brain
30	chr7:149744000-149744600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
31	chr7:149744000-149745600	Active TSS	Right Atrium	heart
32	chr7:149744000-149745800	Active TSS	Stomach Smooth Muscle	stomach
33	chr7:149744000-149746200	Active TSS	Brain Hippocampus Middle	brain
34	chr7:149744000-149746400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
35	chr7:149744000-149746400	Active TSS	Fetal Brain Female	brain
36	chr7:149744000-149746400	Active TSS	HepG2	liver
37	chr7:149744000-149746600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
38	chr7:149744000-149746600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
39	chr7:149744000-149746600	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr7:149744000-149746800	Active TSS	H9 Cell Line	embryonic stem cell
41	chr7:149744000-149746800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
42	chr7:149744000-149746800	Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr7:149744200-149744400	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chr7:149744200-149744400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
45	chr7:149744200-149744400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr7:149744200-149744600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:149744200-149744600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
48	chr7:149744200-149745800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
49	chr7:149744200-149745800	Weak transcription	Fetal Brain Male	brain
50	chr7:149744200-149746400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell

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