Variant report

Variant	nsv608339
Chromosome Location	chr7:123930549-123994631
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	chr7:123953326-123953442	K562	blood:	n/a	n/a
2	ATF1	chr7:123950919-123951365	K562	blood:	n/a	n/a
3	CEBPB	chr7:123950894-123951209	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr7:123950862-123951209	IMR90	lung:	n/a	n/a
5	CEBPB	chr7:123950918-123951174	HepG2	liver:	n/a	n/a
6	CEBPB	chr7:123977376-123977659	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:123950885-123951358	HCT-116	colon:	n/a	n/a
8	CTCF	chr7:123974360-123974510	SK-N-SH_RA	brain:	n/a	n/a
9	E2F4	chr7:123940543-123940569	MCF10A-Er-Src	breast:	n/a	n/a
10	E2F4	chr7:123958475-123958895	MCF10A-Er-Src	breast:	n/a	n/a
11	E2F4	chr7:123960490-123960690	MCF10A-Er-Src	breast:	n/a	n/a
12	EBF1	chr7:123989580-123989791	GM12878	blood:	n/a	chr7:123989686-123989697
13	EBF1	chr7:123989505-123989778	GM12878	blood:	n/a	chr7:123989686-123989697
14	EP300	chr7:123950937-123951148	Hela-S3	cervix:	n/a	n/a
15	FOS	chr7:123962631-123962961	MCF10A-Er-Src	breast:	n/a	chr7:123962785-123962795 chr7:123962786-123962793 chr7:123962786-123962794 chr7:123962791-123962800
16	FOS	chr7:123962617-123962978	MCF10A-Er-Src	breast:	n/a	chr7:123962785-123962795 chr7:123962786-123962793 chr7:123962786-123962794 chr7:123962791-123962800
17	FOS	chr7:123951000-123951108	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr7:123979066-123979104	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr7:123962630-123962960	MCF10A-Er-Src	breast:	n/a	chr7:123962785-123962795 chr7:123962786-123962793 chr7:123962786-123962794 chr7:123962791-123962800
20	FOS	chr7:123950908-123951180	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr7:123962617-123962965	MCF10A-Er-Src	breast:	n/a	chr7:123962785-123962795 chr7:123962786-123962793 chr7:123962786-123962794 chr7:123962791-123962800
22	FOS	chr7:123989556-123989756	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr7:123951011-123951087	MCF10A-Er-Src	breast:	n/a	n/a
24	GATA2	chr7:123991993-123992412	SH-SY5Y	brain:	n/a	n/a
25	GATA3	chr7:123948768-123948776	SH-SY5Y	brain:	n/a	n/a
26	GATA3	chr7:123935157-123935257	SH-SY5Y	brain:	n/a	n/a
27	GATA3	chr7:123961618-123961626	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr7:123993337-123993528	SH-SY5Y	brain:	n/a	n/a
29	GATA3	chr7:123962031-123962065	SH-SY5Y	brain:	n/a	n/a
30	IRF3	chr7:123951136-123951153	GM12878	blood:	n/a	n/a
31	JUN	chr7:123935975-123936054	K562	blood:	n/a	n/a
32	JUN	chr7:123964431-123964612	K562	blood:	n/a	chr7:123964476-123964484
33	JUN	chr7:123946870-123946897	K562	blood:	n/a	n/a
34	JUN	chr7:123993264-123993464	K562	blood:	n/a	n/a
35	JUN	chr7:123968372-123968648	K562	blood:	n/a	n/a
36	JUND	chr7:123952901-123952978	HepG2	liver:	n/a	n/a
37	MAFF	chr7:123947738-123947931	K562	blood:	n/a	chr7:123947829-123947847
38	MAFF	chr7:123935399-123935657	K562	blood:	n/a	chr7:123935531-123935545 chr7:123935525-123935543
39	MAFF	chr7:123935379-123935711	HepG2	liver:	n/a	chr7:123935531-123935545 chr7:123935525-123935543
40	MAFF	chr7:123947701-123947988	HepG2	liver:	n/a	chr7:123947829-123947847
41	MAFK	chr7:123935379-123935763	IMR90	lung:	n/a	chr7:123935531-123935545 chr7:123935528-123935548 chr7:123935530-123935546 chr7:123935527-123935542
42	MAFK	chr7:123948607-123948673	H1-hESC	embryonic stem cell:	n/a	n/a
43	MAFK	chr7:123947698-123947990	IMR90	lung:	n/a	chr7:123947831-123947846 chr7:123947834-123947850 chr7:123947832-123947852
44	MAFK	chr7:123935357-123935715	HepG2	liver:	n/a	chr7:123935531-123935545 chr7:123935528-123935548 chr7:123935530-123935546 chr7:123935527-123935542
45	MAFK	chr7:123935417-123935611	H1-hESC	embryonic stem cell:	n/a	chr7:123935531-123935545 chr7:123935528-123935548 chr7:123935530-123935546 chr7:123935527-123935542
46	MAFK	chr7:123935413-123935714	K562	blood:	n/a	chr7:123935531-123935545 chr7:123935528-123935548 chr7:123935530-123935546 chr7:123935527-123935542
47	MAFK	chr7:123947813-123947923	Hela-S3	cervix:	n/a	chr7:123947831-123947846 chr7:123947834-123947850 chr7:123947832-123947852
48	MAFK	chr7:123955947-123956090	HepG2	liver:	n/a	n/a
49	MAFK	chr7:123947682-123947976	HepG2	liver:	n/a	chr7:123947831-123947846 chr7:123947834-123947850 chr7:123947832-123947852
50	MAFK	chr7:123948503-123948715	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:123992223-123992273	AG10803	skin:	n/a
2	chr7:123992223-123992273	K562	blood:	n/a
3	chr7:123978181-123978231	PFSK-1	brain:	n/a
4	chr7:123992223-123992273	PANC-1	pancreas:	n/a
5	chr7:123992223-123992273	HAEpiC	amniotic membrane:	n/a
6	chr7:123978181-123978231	HCM	heart:	n/a
7	chr7:123978181-123978231	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:123992223-123992273	MCF-7	breast:	n/a
9	chr7:123992223-123992273	GM06990	blood:	n/a
10	chr7:123978181-123978231	ProgFib	skin:	n/a
11	chr7:123992223-123992273	HEEpiC	esophagus:	n/a
12	chr7:123992223-123992273	HCM	heart:	n/a
13	chr7:123978181-123978231	HUVEC	blood vessel:	n/a
14	chr7:123992223-123992273	ECC-1	luminal epithelium:	n/a
15	chr7:123978181-123978231	GM12892	blood:	n/a
16	chr7:123978181-123978231	HepG2	liver:	n/a
17	chr7:123992223-123992273	SK-N-SH	brain:	n/a
18	chr7:123978181-123978231	HRPEpiC	eye:	n/a
19	chr7:123978181-123978231	PrEC	prostate:	n/a
20	chr7:123978181-123978231	AG04449	skin:	fetal
21	chr7:123978181-123978231	GM06990	blood:	n/a
22	chr7:123978181-123978231	Jurkat	blood:	n/a
23	chr7:123978181-123978231	GM12891	blood:	n/a
24	chr7:123992223-123992273	HNPCEpiC	eye:	n/a
25	chr7:123978181-123978231	HMEC	breast:	n/a
26	chr7:123978181-123978231	HRCEpiC	kidney:	n/a
27	chr7:123992223-123992273	BJ	skin:	n/a
28	chr7:123978181-123978231	T-47D	breast:	n/a
29	chr7:123978181-123978231	LNCaP	prostate:	n/a
30	chr7:123992223-123992273	GM19239	blood:	n/a
31	chr7:123978181-123978231	ovcar-3	ovarian:	n/a
32	chr7:123992223-123992273	SK-N-MC	brain:	n/a
33	chr7:123992223-123992273	HRPEpiC	eye:	n/a
34	chr7:123978181-123978231	CMK	blood:	n/a
35	chr7:123992223-123992273	BE2_C	brain:	n/a
36	chr7:123978181-123978231	NH-A	brain:	n/a
37	chr7:123978181-123978231	HRE	kidney:	n/a
38	chr7:123978181-123978231	SK-N-SH	brain:	n/a
39	chr7:123992223-123992273	ovcar-3	ovarian:	n/a
40	chr7:123992223-123992273	NT2-D1	testis:	n/a
41	chr7:123992223-123992273	GM12891	blood:	n/a
42	chr7:123992223-123992273	Jurkat	blood:	n/a
43	chr7:123978181-123978231	HCT-116	colon:	n/a
44	chr7:123992223-123992273	PFSK-1	brain:	n/a
45	chr7:123992223-123992273	MCF10A-Er-Src	breast:	n/a
46	chr7:123978181-123978231	NHBE	bronchial:	n/a
47	chr7:123992223-123992273	HCF	heart:	n/a
48	chr7:123992223-123992273	H1-hESC	embryonic stem cell:	embryo
49	chr7:123978181-123978231	ECC-1	luminal epithelium:	n/a
50	chr7:123978181-123978231	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:123973378..123975261-chr7:123975911..123978785,2	K562	blood:
2	chr7:123919958..123922914-chr7:123935794..123937294,2	K562	blood:
3	chr3:64234460..64234993-chr7:123973379..123973879,2	MCF-7	breast:
4	chr7:123938093..123940517-chr7:124074999..124077404,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM229A-2	chr7:123977434-123977554	XLOC_006591
2	lnc-TMEM229A-2	chr7:123989883-123989978	NR_110180
3	lnc-SPAM1-3	chr7:123992870-123992905	ENSG00000242593.1
4	lnc-TMEM229A-2	chr7:123977434-123977554	NR_110180
5	lnc-TMEM229A-2	chr7:123977434-123977554	XLOC_006591
6	lnc-SPAM1-3	chr7:123993205-123993469	XLOC_006228
7	lnc-TMEM229A-2	chr7:123991905-123992150	NR_110180
8	lnc-TMEM229A-2	chr7:123991905-123992154	XLOC_006591
9	lnc-SPAM1-3	chr7:123992870-123992905	XLOC_006228
10	lnc-TMEM229A-2	chr7:123982515-123982615	XLOC_006591
11	lnc-TMEM229A-2	chr7:123989883-123989978	XLOC_006591
12	lnc-TMEM229A-2	chr7:123982515-123982615	NR_110180
13	lnc-SPAM1-3	chr7:123974348-123974485	XLOC_006228
14	lnc-TMEM229A-2	chr7:123982515-123982615	XLOC_006591
15	lnc-TMEM229A-2	chr7:123989883-123989914	XLOC_006591

Variant related genes	Relation type
ENSG00000242593	TF binding region
ENSG00000243574	TF binding region
ENSG00000241324	TF binding region
ENSG00000242593	CpG island
ENSG00000243574	CpG island
ENSG00000241324	CpG island
ENSG00000242593	chromatin interactions

Extended variants
information (count: 822 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:822 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144776141	chr7:123951025-123951026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs386717440	chr7:123951026-123951027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs201254401	chr7:123951029-123951030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566724402	chr7:123951030-123951031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs71574793	chr7:123951042-123951043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150007667	chr7:123951057-123951058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs146099465	chr7:123951111-123951112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140087724	chr7:123951115-123951116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537690933	chr7:123951191-123951192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554329394	chr7:123951192-123951193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73431419	chr7:123951242-123951243	Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs73722105	chr7:123951267-123951268	Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs544062693	chr7:123951270-123951271	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs143548714	chr7:123951301-123951302	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs146789130	chr7:123951307-123951308	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs545884105	chr7:123951377-123951378	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs562488204	chr7:123951394-123951395	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs77329226	chr7:123951399-123951400	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs541634017	chr7:123951436-123951437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181845299	chr7:123951440-123951441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs56152509	chr7:123951452-123951453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73722106	chr7:123951486-123951487	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs574230030	chr7:123951506-123951507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184875907	chr7:123951511-123951512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552534519	chr7:123951520-123951521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569045278	chr7:123951557-123951558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7784625	chr7:123951585-123951586	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs370925903	chr7:123951681-123951682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142999789	chr7:123951682-123951683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567882320	chr7:123951702-123951703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559655470	chr7:123951730-123951731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528489925	chr7:123951768-123951769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541292753	chr7:123951784-123951785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564255137	chr7:123951786-123951787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188838552	chr7:123951790-123951791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532947508	chr7:123951796-123951797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561929417	chr7:123951821-123951822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7785063	chr7:123951835-123951836	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs180704508	chr7:123951841-123951842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79178518	chr7:123951854-123951855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569409548	chr7:123951911-123951912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539100160	chr7:123951925-123951926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185335272	chr7:123951929-123951930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73722107	chr7:123951948-123951949	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs541917454	chr7:123951974-123951975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529739717	chr7:123952008-123952009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561481513	chr7:123952026-123952027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs151087105	chr7:123952079-123952080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547812511	chr7:123952083-123952084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540819008	chr7:123952126-123952127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:123951000-123951400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr7:123951200-123951400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:123951200-123951400	ZNF genes & repeats	Pancreas	Pancrea
4	chr7:123951400-123956000	Weak transcription	Pancreas	Pancrea
5	chr7:123953400-123954400	Enhancers	Fetal Lung	lung
6	chr7:123954400-123956600	Weak transcription	Fetal Lung	lung
7	chr7:123956000-123956200	ZNF genes & repeats	Pancreas	Pancrea
8	chr7:123956600-123959200	Enhancers	Fetal Lung	lung
9	chr7:123962400-123962600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr7:123962600-123963600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr7:123963600-123964200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr7:123964200-123964600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr7:123964600-123965200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr7:123968200-123969200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr7:123970000-123970600	Enhancers	Fetal Lung	lung
16	chr7:123970400-123971400	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr7:123973400-123973600	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr7:123974200-123974600	Enhancers	Fetal Brain Female	brain
19	chr7:123978800-123979200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:123991400-123995400	Enhancers	Fetal Brain Male	brain
21	chr7:123991600-123992600	Enhancers	Fetal Heart	heart
22	chr7:123991800-123992000	Enhancers	Brain Anterior Caudate	brain
23	chr7:123991800-123992000	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr7:123991800-123994600	Enhancers	Fetal Brain Female	brain
25	chr7:123992000-123992200	Active TSS	Brain Angular Gyrus	brain
26	chr7:123992000-123992200	Active TSS	Brain Cingulate Gyrus	brain
27	chr7:123992000-123992200	Active TSS	Right Ventricle	heart
28	chr7:123992000-123992400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr7:123992000-123992400	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr7:123992000-123992400	Flanking Active TSS	Brain Anterior Caudate	brain
31	chr7:123992000-123992400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
32	chr7:123992000-123992600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr7:123992000-123992600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr7:123992000-123992600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr7:123992200-123992400	Flanking Active TSS	Brain Angular Gyrus	brain
36	chr7:123992200-123992400	Flanking Active TSS	Brain Cingulate Gyrus	brain
37	chr7:123992200-123992400	Flanking Active TSS	Right Ventricle	heart
38	chr7:123992200-123992600	Enhancers	Brain Hippocampus Middle	brain
39	chr7:123992200-123992600	Enhancers	Brain Substantia Nigra	brain
40	chr7:123992400-123992600	Enhancers	Brain Cingulate Gyrus	brain

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