Variant report

Variant	nsv831117
Chromosome Location	chr7:123957376-124089186
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:224)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:224 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:124026607-124026805	K562	blood:	n/a	n/a
2	BACH1	chr7:124009494-124009604	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr7:124019650-124019721	K562	blood:	n/a	n/a
4	CEBPB	chr7:124064832-124064918	A549	lung:	n/a	n/a
5	CEBPB	chr7:124059870-124060070	A549	lung:	n/a	chr7:124059953-124059964
6	CEBPB	chr7:124059848-124060080	K562	blood:	n/a	chr7:124059953-124059964
7	CEBPB	chr7:124013877-124014110	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr7:124059833-124060117	HepG2	liver:	n/a	chr7:124059953-124059964
9	CEBPB	chr7:124009431-124009635	MCF-7	breast:	n/a	n/a
10	CEBPB	chr7:124013792-124014147	HepG2	liver:	n/a	n/a
11	CEBPB	chr7:124057226-124057493	HepG2	liver:	n/a	chr7:124057404-124057417
12	CEBPB	chr7:124006073-124006379	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:124035162-124035516	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:124048967-124049360	HepG2	liver:	n/a	chr7:124049338-124049351
15	CEBPB	chr7:124013825-124014114	A549	lung:	n/a	n/a
16	CEBPB	chr7:124009369-124009705	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:124000893-124001093	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:124035204-124035481	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:124013819-124014135	IMR90	lung:	n/a	n/a
20	CEBPB	chr7:124059840-124060094	IMR90	lung:	n/a	chr7:124059953-124059964
21	CEBPB	chr7:124013810-124014125	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:124035161-124035500	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr7:124059922-124059972	H1-hESC	embryonic stem cell:	n/a	chr7:124059953-124059964
24	CEBPB	chr7:124013892-124014116	K562	blood:	n/a	n/a
25	CEBPB	chr7:124035154-124035475	A549	lung:	n/a	n/a
26	CEBPB	chr7:123977376-123977659	HepG2	liver:	n/a	n/a
27	CEBPB	chr7:124027875-124028066	HepG2	liver:	n/a	chr7:124027967-124027978
28	CHD2	chr7:124009518-124009694	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr7:124014999-124015035	LNCaP	prostate:	n/a	n/a
30	CTCF	chr7:124059440-124059590	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr7:123974360-123974510	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr7:124078040-124078190	GM12865	blood:	n/a	n/a
33	CTCF	chr7:124007080-124007105	GM20000	blood:	n/a	n/a
34	E2F4	chr7:123958475-123958895	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr7:123960490-123960690	MCF10A-Er-Src	breast:	n/a	n/a
36	EBF1	chr7:123989505-123989778	GM12878	blood:	n/a	chr7:123989686-123989697
37	EBF1	chr7:123989580-123989791	GM12878	blood:	n/a	chr7:123989686-123989697
38	EP300	chr7:124027071-124027462	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr7:124060391-124060717	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr7:124067447-124067496	GM12878	blood:	n/a	n/a
41	EP300	chr7:124027093-124027528	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr7:124026712-124028137	SK-N-SH	brain:	n/a	chr7:124028020-124028034 chr7:124028019-124028033 chr7:124028018-124028032
43	FOS	chr7:124080214-124080462	MCF10A-Er-Src	breast:	n/a	chr7:124080314-124080323 chr7:124080313-124080322 chr7:124080314-124080321 chr7:124080314-124080322
44	FOS	chr7:123962617-123962978	MCF10A-Er-Src	breast:	n/a	chr7:123962785-123962795 chr7:123962786-123962793 chr7:123962786-123962794 chr7:123962791-123962800
45	FOS	chr7:123962630-123962960	MCF10A-Er-Src	breast:	n/a	chr7:123962785-123962795 chr7:123962786-123962793 chr7:123962786-123962794 chr7:123962791-123962800
46	FOS	chr7:124047947-124048179	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr7:123962631-123962961	MCF10A-Er-Src	breast:	n/a	chr7:123962785-123962795 chr7:123962786-123962793 chr7:123962786-123962794 chr7:123962791-123962800
48	FOS	chr7:123996075-123996179	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr7:124080187-124080506	MCF10A-Er-Src	breast:	n/a	chr7:124080314-124080323 chr7:124080313-124080322 chr7:124080314-124080321 chr7:124080314-124080322
50	FOS	chr7:123962617-123962965	MCF10A-Er-Src	breast:	n/a	chr7:123962785-123962795 chr7:123962786-123962793 chr7:123962786-123962794 chr7:123962791-123962800

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:123978181-123978231	ovcar-3	ovarian:	n/a
2	chr7:123992223-123992273	HEEpiC	esophagus:	n/a
3	chr7:123992223-123992273	SKMC	muscle:	n/a
4	chr7:123978181-123978231	ProgFib	skin:	n/a
5	chr7:123978181-123978231	BJ	skin:	n/a
6	chr7:123978181-123978231	HRPEpiC	eye:	n/a
7	chr7:123992223-123992273	CMK	blood:	n/a
8	chr7:123978181-123978231	AoSMC	blood vessel:	n/a
9	chr7:123978181-123978231	GM12891	blood:	n/a
10	chr7:123978181-123978231	IMR90	lung:	fetal
11	chr7:123978181-123978231	HCF	heart:	n/a
12	chr7:123978181-123978231	T-47D	breast:	n/a
13	chr7:123978181-123978231	HAEpiC	amniotic membrane:	n/a
14	chr7:123992223-123992273	MCF-7	breast:	n/a
15	chr7:123978181-123978231	GM19239	blood:	n/a
16	chr7:123992223-123992273	GM12891	blood:	n/a
17	chr7:123992223-123992273	GM19239	blood:	n/a
18	chr7:123992223-123992273	K562	blood:	n/a
19	chr7:123978181-123978231	SK-N-SH	brain:	n/a
20	chr7:123992223-123992273	HRPEpiC	eye:	n/a
21	chr7:123978181-123978231	NB4	blood:	n/a
22	chr7:123992223-123992273	U87	brain:	n/a
23	chr7:123992223-123992273	HL-60	blood:	n/a
24	chr7:123992223-123992273	HEK293	kidney:	embryo
25	chr7:123978181-123978231	PFSK-1	brain:	n/a
26	chr7:123992223-123992273	RPTEC	kidney:	n/a
27	chr7:123992223-123992273	HMEC	breast:	n/a
28	chr7:123978181-123978231	NHBE	bronchial:	n/a
29	chr7:123992223-123992273	AG04450	lung:	fetal
30	chr7:123978181-123978231	Hepatocyte	liver:	n/a
31	chr7:123978181-123978231	PANC-1	pancreas:	n/a
32	chr7:123992223-123992273	T-47D	breast:	n/a
33	chr7:123992223-123992273	Hela-S3	cervix:	n/a
34	chr7:123978181-123978231	U87	brain:	n/a
35	chr7:123978181-123978231	HUVEC	blood vessel:	n/a
36	chr7:123992223-123992273	PANC-1	pancreas:	n/a
37	chr7:123978181-123978231	HIPEpiC	eye:	n/a
38	chr7:123992223-123992273	SK-N-MC	brain:	n/a
39	chr7:123978181-123978231	SK-N-SH_RA	brain:	n/a
40	chr7:123978181-123978231	AG04449	skin:	fetal
41	chr7:123978181-123978231	HNPCEpiC	eye:	n/a
42	chr7:123992223-123992273	A549	lung:	n/a
43	chr7:123978181-123978231	HL-60	blood:	n/a
44	chr7:123978181-123978231	Caco-2	colon:	n/a
45	chr7:123992223-123992273	AG09319	gingival:	n/a
46	chr7:123992223-123992273	SK-N-SH_RA	brain:	n/a
47	chr7:123992223-123992273	Jurkat	blood:	n/a
48	chr7:123992223-123992273	Caco-2	colon:	n/a
49	chr7:123978181-123978231	LNCaP	prostate:	n/a
50	chr7:123992223-123992273	NT2-D1	testis:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:124045286..124047206-chr7:124048009..124050452,2	K562	blood:
2	chr7:124087717..124091760-chr7:124402640..124406846,5	MCF-7	breast:
3	chr7:124086263..124087904-chr7:124128230..124129878,2	MCF-7	breast:
4	chr7:123996206..123998785-chr8:77412686..77415296,2	MCF-7	breast:
5	chr7:123973378..123975261-chr7:123975911..123978785,2	K562	blood:
6	chr3:64234460..64234993-chr7:123973379..123973879,2	MCF-7	breast:
7	chr7:123938093..123940517-chr7:124074999..124077404,2	K562	blood:
8	chr7:124086521..124089407-chr7:124092308..124093904,2	MCF-7	breast:
9	chr7:124082576..124084673-chr7:124100575..124102753,2	K562	blood:
10	chr7:124018038..124020966-chr7:124025116..124027291,2	MCF-7	breast:
11	chr7:124082317..124084837-chr7:124085340..124087989,2	K562	blood:
12	chr7:124018038..124020966-chr7:124025116..124027291,2	MCF-7	breast:
13	chr7:124082317..124084837-chr7:124085340..124087989,2	K562	blood:
14	chr7:124087958..124089614-chr7:124089857..124091859,2	MCF-7	breast:
15	chr7:124045286..124047206-chr7:124048009..124050452,2	K562	blood:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAM1-3	chr7:123992870-123992905	ENSG00000242593.1
2	lnc-SPAM1-3	chr7:124028495-124028581	NONHSAT123082
3	lnc-TMEM229A-2	chr7:123989883-123989914	XLOC_006591
4	lnc-TMEM229A-2	chr7:123977434-123977554	XLOC_006591
5	lnc-TMEM229A-2	chr7:123982515-123982615	XLOC_006591
6	lnc-SPAM1-3	chr7:124000163-124000252	ENSG00000242593.1
7	lnc-TMEM229A-2	chr7:123991905-123992154	XLOC_006591
8	lnc-SPAM1-3	chr7:124031483-124035172	ENSG00000242593.1
9	lnc-SPAM1-3	chr7:124029526-124029556	XLOC_006229
10	lnc-TMEM229A-2	chr7:123977434-123977554	XLOC_006591
11	lnc-TMEM229A-2	chr7:123991905-123992150	NR_110180
12	lnc-SPAM1-3	chr7:124029526-124029610	ENSG00000242593.1
13	lnc-TMEM229A-2	chr7:123977434-123977554	NR_110180
14	lnc-SPAM1-3	chr7:124029526-124029610	NONHSAT123082
15	lnc-SPAM1-3	chr7:123974348-123974485	XLOC_006228
16	lnc-TMEM229A-2	chr7:123989883-123989978	XLOC_006591
17	lnc-SPAM1-3	chr7:123992870-123992905	XLOC_006228
18	lnc-SPAM1-3	chr7:124032563-124032795	NONHSAT123082
19	lnc-TMEM229A-2	chr7:123982515-123982615	XLOC_006591
20	lnc-SPAM1-3	chr7:124025652-124025703	ENSG00000242593.1
21	lnc-SPAM1-3	chr7:124028468-124028581	ENSG00000242593.1
22	lnc-SPAM1-3	chr7:123993205-123993469	XLOC_006228
23	lnc-TMEM229A-2	chr7:123989883-123989978	NR_110180
24	lnc-SPAM1-3	chr7:124016376-124016450	ENSG00000242593.1
25	lnc-SPAM1-3	chr7:124027821-124028581	XLOC_006229
26	lnc-TMEM229A-2	chr7:123982515-123982615	NR_110180

No data

Variant related genes	Relation type
ENSG00000242593	TF binding region
ENSG00000241324	TF binding region
ENSG00000242593	CpG island
ENSG00000241324	CpG island
ENSG00000242593	chromatin interactions
ENSG00000170775	chromatin interactions

Extended variants
information (count: 2086 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2086 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112915332	chr7:123957412-123957413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs189702822	chr7:123957447-123957448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs17146944	chr7:123957448-123957449	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs533071504	chr7:123957477-123957478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528977222	chr7:123957479-123957480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs397808800	chr7:123957490-123957491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544815694	chr7:123957496-123957497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs561464443	chr7:123957504-123957505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs375739262	chr7:123957507-123957508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141183925	chr7:123957508-123957509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546706045	chr7:123957524-123957525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560503723	chr7:123957585-123957586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532479862	chr7:123957600-123957601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370485222	chr7:123957633-123957634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569008632	chr7:123957674-123957675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537677940	chr7:123957693-123957694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146083659	chr7:123957694-123957695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113693972	chr7:123957721-123957722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs13241184	chr7:123957799-123957800	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs370665582	chr7:123957828-123957829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568295595	chr7:123957835-123957836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201336259	chr7:123957843-123957844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530463730	chr7:123957874-123957875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs7807675	chr7:123957875-123957876	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs553500515	chr7:123957879-123957880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570418745	chr7:123957907-123957908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146970357	chr7:123957908-123957909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540146413	chr7:123957915-123957916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs113272696	chr7:123957918-123957919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556339010	chr7:123958014-123958015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529103213	chr7:123958048-123958049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs13241533	chr7:123958058-123958059	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs538718322	chr7:123958081-123958082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150929439	chr7:123958098-123958099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs367954596	chr7:123958107-123958108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114524378	chr7:123958128-123958129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs79911112	chr7:123958170-123958171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540880278	chr7:123958172-123958173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs11765479	chr7:123958189-123958190	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs556827591	chr7:123958201-123958202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188893930	chr7:123958276-123958277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532415691	chr7:123958310-123958311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs193101210	chr7:123958381-123958382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs376880877	chr7:123958428-123958429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183566607	chr7:123958437-123958438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73722111	chr7:123958597-123958598	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs542909912	chr7:123958604-123958605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs187583055	chr7:123958669-123958670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531668987	chr7:123958700-123958701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559240441	chr7:123958723-123958724	Enhancers	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:128 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:123956600-123959200	Enhancers	Fetal Lung	lung
2	chr7:123962400-123962600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr7:123962600-123963600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr7:123963600-123964200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr7:123964200-123964600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:123964600-123965200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr7:123968200-123969200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr7:123970000-123970600	Enhancers	Fetal Lung	lung
9	chr7:123970400-123971400	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr7:123973400-123973600	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr7:123974200-123974600	Enhancers	Fetal Brain Female	brain
12	chr7:123978800-123979200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr7:123991400-123995400	Enhancers	Fetal Brain Male	brain
14	chr7:123991600-123992600	Enhancers	Fetal Heart	heart
15	chr7:123991800-123992000	Enhancers	Brain Anterior Caudate	brain
16	chr7:123991800-123992000	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr7:123991800-123994600	Enhancers	Fetal Brain Female	brain
18	chr7:123992000-123992200	Active TSS	Brain Angular Gyrus	brain
19	chr7:123992000-123992200	Active TSS	Brain Cingulate Gyrus	brain
20	chr7:123992000-123992200	Active TSS	Right Ventricle	heart
21	chr7:123992000-123992400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr7:123992000-123992400	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr7:123992000-123992400	Flanking Active TSS	Brain Anterior Caudate	brain
24	chr7:123992000-123992400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr7:123992000-123992600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr7:123992000-123992600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr7:123992000-123992600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr7:123992200-123992400	Flanking Active TSS	Brain Angular Gyrus	brain
29	chr7:123992200-123992400	Flanking Active TSS	Brain Cingulate Gyrus	brain
30	chr7:123992200-123992400	Flanking Active TSS	Right Ventricle	heart
31	chr7:123992200-123992600	Enhancers	Brain Hippocampus Middle	brain
32	chr7:123992200-123992600	Enhancers	Brain Substantia Nigra	brain
33	chr7:123992400-123992600	Enhancers	Brain Cingulate Gyrus	brain
34	chr7:123997200-124000000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:124002800-124003000	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr7:124003000-124004200	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr7:124004200-124005800	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr7:124009200-124009800	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr7:124009200-124010000	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr7:124009600-124010000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr7:124009600-124010000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr7:124009600-124010400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr7:124015200-124020800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr7:124027400-124028000	Enhancers	Brain Hippocampus Middle	brain
45	chr7:124027600-124027800	Enhancers	Brain Substantia Nigra	brain
46	chr7:124027800-124030800	Weak transcription	Brain Substantia Nigra	brain
47	chr7:124028000-124030800	Weak transcription	Brain Hippocampus Middle	brain
48	chr7:124030400-124033800	Weak transcription	Fetal Brain Male	brain
49	chr7:124030600-124031600	Enhancers	Brain Cingulate Gyrus	brain
50	chr7:124030800-124031800	Enhancers	Brain Substantia Nigra	brain

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