Variant report

Variant	nsv889439
Chromosome Location	chr7:149667270-149786096
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	chr7:149700297-149700734	K562	blood:	n/a	n/a
2	ATF1	chr7:149742080-149742094	K562	blood:	n/a	n/a
3	BACH1	chr7:149746378-149746646	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:149672891-149673080	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr7:149757655-149757938	GM12878	blood:	n/a	chr7:149757827-149757838
6	BATF	chr7:149743485-149743750	GM12878	blood:	n/a	n/a
7	CEBPB	chr7:149784693-149784950	HepG2	liver:	n/a	chr7:149784796-149784807
8	CEBPB	chr7:149701434-149701491	K562	blood:	n/a	n/a
9	CEBPB	chr7:149701346-149701464	A549	lung:	n/a	n/a
10	CEBPB	chr7:149701451-149701643	IMR90	lung:	n/a	n/a
11	CEBPB	chr7:149667593-149667795	HepG2	liver:	n/a	chr7:149667743-149667754
12	CEBPB	chr7:149667610-149667796	K562	blood:	n/a	chr7:149667743-149667754
13	CEBPB	chr7:149713771-149714042	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:149684112-149684277	K562	blood:	n/a	chr7:149684215-149684232
15	CEBPB	chr7:149667622-149667822	IMR90	lung:	n/a	chr7:149667743-149667754
16	CEBPB	chr7:149684147-149684317	H1-hESC	embryonic stem cell:	n/a	chr7:149684215-149684232
17	CEBPB	chr7:149684039-149684320	K562	blood:	n/a	chr7:149684215-149684232
18	CHD1	chr7:149746398-149746684	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr7:149746382-149746488	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr7:149743085-149743097	LNCaP	prostate:	n/a	n/a
21	CTCF	chr7:149757620-149757770	HepG2	liver:	n/a	n/a
22	CTCF	chr7:149757523-149757948	A549	lung:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
23	CTCF	chr7:149698323-149698546	K562	blood:	n/a	n/a
24	CTCF	chr7:149746320-149746470	BE2_C	brain:	n/a	n/a
25	CTCF	chr7:149742780-149742930	GM06990	blood:	n/a	n/a
26	CTCF	chr7:149722323-149722404	Lung_OC	lung:	n/a	chr7:149722360-149722381 chr7:149722365-149722383
27	CTCF	chr7:149746070-149746366	MCF-7	breast:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
28	CTCF	chr7:149742820-149742970	HAc	cerebellar:	n/a	n/a
29	CTCF	chr7:149781960-149782110	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr7:149757649-149757902	MCF-7	breast:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
31	CTCF	chr7:149744020-149744170	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:149757635-149757907	HUVEC	blood vessel:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
33	CTCF	chr7:149746168-149746303	GM10248	blood:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
34	CTCF	chr7:149698460-149698610	GM12874	blood:	n/a	n/a
35	CTCF	chr7:149757656-149757904	MCF-7	breast:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
36	CTCF	chr7:149675654-149675851	LNCaP	prostate:	n/a	chr7:149675758-149675779 chr7:149675756-149675774
37	CTCF	chr7:149746320-149746470	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr7:149746082-149746379	Medullo	brain:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
39	CTCF	chr7:149745900-149746050	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr7:149745917-149746469	K562	blood:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
41	CTCF	chr7:149675840-149675990	A549	lung:	n/a	n/a
42	CTCF	chr7:149757620-149757911	Gliobla	brain:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
43	CTCF	chr7:149746030-149746330	H1-hESC	embryonic stem cell:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
44	CTCF	chr7:149675740-149675778	GM19239	blood:	n/a	chr7:149675756-149675774
45	CTCF	chr7:149757660-149757810	HRPEpiC	eye:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
46	CTCF	chr7:149757626-149757919	LNCaP	prostate:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
47	CTCF	chr7:149737961-149737980	LNCaP	prostate:	n/a	n/a
48	CTCF	chr7:149746388-149746455	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr7:149757634-149757918	GM10266	blood:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
50	CTCF	chr7:149698220-149698510	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:149732847-149732897	HNPCEpiC	eye:	n/a
2	chr7:149744935-149744985	Hela-S3	cervix:	n/a
3	chr7:149732847-149732897	HNPCEpiC	eye:	n/a
4	chr7:149744935-149744985	Hela-S3	cervix:	n/a
5	chr7:149746640-149746690	NT2-D1	testis:	n/a
6	chr7:149732847-149732897	Jurkat	blood:	n/a
7	chr7:149749941-149749991	AG10803	skin:	n/a
8	chr7:149780548-149780598	Caco-2	colon:	n/a
9	chr7:149744597-149744647	CMK	blood:	n/a
10	chr7:149732579-149732629	LNCaP	prostate:	n/a
11	chr7:149780548-149780598	GM12892	blood:	n/a
12	chr7:149738501-149738551	AoSMC	blood vessel:	n/a
13	chr7:149733821-149733871	HEEpiC	esophagus:	n/a
14	chr7:149749941-149749991	ECC-1	luminal epithelium:	n/a
15	chr7:149731742-149731792	K562	blood:	n/a
16	chr7:149733103-149733153	HNPCEpiC	eye:	n/a
17	chr7:149749941-149749991	PANC-1	pancreas:	n/a
18	chr7:149745299-149745349	RPTEC	kidney:	n/a
19	chr7:149745299-149745349	HIPEpiC	eye:	n/a
20	chr7:149744041-149744091	NB4	blood:	n/a
21	chr7:149744935-149744985	K562	blood:	n/a
22	chr7:149735726-149735776	Jurkat	blood:	n/a
23	chr7:149733103-149733153	RPTEC	kidney:	n/a
24	chr7:149732847-149732897	GM06990	blood:	n/a
25	chr7:149780548-149780598	GM12891	blood:	n/a
26	chr7:149749941-149749991	ProgFib	skin:	n/a
27	chr7:149733821-149733871	K562	blood:	n/a
28	chr7:149746468-149746518	GM19239	blood:	n/a
29	chr7:149736127-149736177	AG04449	skin:	fetal
30	chr7:149735729-149735779	NHDF-neo	bronchial:	n/a
31	chr7:149731767-149731817	ProgFib	skin:	n/a
32	chr7:149742121-149742171	HAEpiC	amniotic membrane:	n/a
33	chr7:149733103-149733153	HMEC	breast:	n/a
34	chr7:149738501-149738551	Jurkat	blood:	n/a
35	chr7:149744041-149744091	MCF-7	breast:	n/a
36	chr7:149780548-149780598	HCM	heart:	n/a
37	chr7:149746468-149746518	AG04449	skin:	fetal
38	chr7:149746640-149746690	IMR90	lung:	fetal
39	chr7:149732847-149732897	NH-A	brain:	n/a
40	chr7:149732579-149732629	GM12892	blood:	n/a
41	chr7:149745299-149745349	NHBE	bronchial:	n/a
42	chr7:149746468-149746518	HCF	heart:	n/a
43	chr7:149734481-149734531	K562	blood:	n/a
44	chr7:149746640-149746690	PrEC	prostate:	n/a
45	chr7:149744935-149744985	A549	lung:	n/a
46	chr7:149738473-149738523	PANC-1	pancreas:	n/a
47	chr7:149735726-149735776	SK-N-SH	brain:	n/a
48	chr7:149746077-149746127	Caco-2	colon:	n/a
49	chr7:149744597-149744647	HepG2	liver:	n/a
50	chr7:149732579-149732629	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:149580322..149580844-chr7:149745955..149746566,2	MCF-7	breast:
2	chr7:149699024..149700856-chr7:153788710..153791500,2	K562	blood:
3	chr7:149757556..149758057-chr7:149919306..149919858,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF467-4	chr7:149699986-149700449	NONHSAT124086
2	lnc-ATP6V0E2-1	chr7:149697841-149700167	ENSG00000249583
3	lnc-ATP6V0E2-2	chr7:149770706-149770828	ENSG00000241449
4	lnc-ATP6V0E2-2	chr7:149770706-149770828	ENSG00000241449
5	lnc-ATP6V0E2-2	chr7:149773639-149773744	ENSG00000241449
6	lnc-ZNF467-4	chr7:149700614-149701513	NONHSAT124086
7	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124091
8	lnc-ATP6V0E2-2	chr7:149761675-149761850	ucscGeneNc_uc003whi_1
9	lnc-ATP6V0E2-7	chr7:149670980-149671663	l_3505_chr7:149670979-149676122_ovary
10	lnc-ATP6V0E2-2	chr7:149771062-149771172	ENSG00000241449
11	lnc-ATP6V0E2-2	chr7:149759178-149759348	ENSG00000241449
12	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124087
13	lnc-ATP6V0E2-2	chr7:149737610-149737743	ENSG00000241449
14	lnc-ATP6V0E2-2	chr7:149775097-149776161	ucscGeneNc_uc003whi_1
15	lnc-ATP6V0E2-2	chr7:149770570-149771181	ucscGeneNc_uc003whi_1
16	lnc-ATP6V0E2-2	chr7:149774721-149774910	ucscGeneNc_uc003whi_1
17	lnc-ATP6V0E2-2	chr7:149738452-149738550	NONHSAT124091
18	lnc-ATP6V0E2-2	chr7:149732185-149732207	NONHSAT124087
19	lnc-ATP6V0E2-2	chr7:149738452-149738550	ENSG00000241449
20	lnc-ATP6V0E2-8	chr7:149697081-149697368	expReg_chr7_12098_+
21	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124088
22	lnc-ATP6V0E2-2	chr7:149735636-149735802	NONHSAT124088
23	lnc-ATP6V0E2-2	chr7:149737556-149737743	NONHSAT124091
24	lnc-ATP6V0E2-2	chr7:149771062-149771465	ENSG00000241449
25	lnc-ATP6V0E2-1	chr7:149701497-149702213	ENSG00000249583
26	lnc-ATP6V0E2-7	chr7:149676088-149676122	l_3505_chr7:149670979-149676122_ovary

Variant related genes	Relation type
ENSG00000241449	TF binding region
ENSG00000260555	TF binding region
ENSG00000241449	CpG island
ENSG00000260555	CpG island
SOCS2	miRNA target sites
JPH1	miRNA target sites

Extended variants
information (count: 4259 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:4259 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4725854	chr7:149667270-149667271	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs200266480	chr7:149667321-149667322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572819764	chr7:149667326-149667327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535333907	chr7:149667337-149667338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139686506	chr7:149667404-149667405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577529246	chr7:149667408-149667409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141814237	chr7:149667532-149667533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554152302	chr7:149667550-149667551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573384220	chr7:149667565-149667566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111447176	chr7:149667578-149667579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs397839715	chr7:149667602-149667603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs71221700	chr7:149667627-149667628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542453167	chr7:149667640-149667641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71307690	chr7:149667655-149667656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs117854964	chr7:149667658-149667659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528371511	chr7:149667662-149667663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551610649	chr7:149667677-149667678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs71221701	chr7:149667690-149667691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554768190	chr7:149667717-149667718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551947038	chr7:149667762-149667763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs71203903	chr7:149667788-149667789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564339371	chr7:149667864-149667865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533331850	chr7:149667909-149667910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs71203904	chr7:149667921-149667922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71203905	chr7:149667933-149667934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs71203906	chr7:149667946-149667947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs71307691	chr7:149667982-149667983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs71307692	chr7:149668036-149668037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549885120	chr7:149668037-149668038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs71534006	chr7:149668052-149668053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs3111982	chr7:149668063-149668064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs71534007	chr7:149668066-149668067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576063600	chr7:149668172-149668173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs199899273	chr7:149668190-149668191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10250634	chr7:149668202-149668203	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs529399572	chr7:149668242-149668243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549648034	chr7:149668244-149668245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566232517	chr7:149668277-149668278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377642208	chr7:149668294-149668295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1385013	chr7:149668321-149668322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs3102292	chr7:149668341-149668342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535019364	chr7:149668407-149668408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142475104	chr7:149668427-149668428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs3102293	chr7:149668441-149668442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs551222257	chr7:149668469-149668470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537080612	chr7:149668482-149668483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs556671601	chr7:149668611-149668612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573447905	chr7:149668631-149668632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190984159	chr7:149668659-149668660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150349892	chr7:149668686-149668687	Weak transcription 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
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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:561 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:149663800-149672000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr7:149666200-149669800	Weak transcription	Pancreas	Pancrea
3	chr7:149666400-149668400	Weak transcription	Brain Hippocampus Middle	brain
4	chr7:149666600-149671400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:149668400-149669000	Enhancers	Brain Hippocampus Middle	brain
6	chr7:149669800-149670400	Enhancers	Pancreas	Pancrea
7	chr7:149670000-149670400	Enhancers	Fetal Intestine Large	intestine
8	chr7:149670000-149670800	Enhancers	Duodenum Mucosa	Duodenum
9	chr7:149670800-149672200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr7:149671400-149672200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:149671600-149671800	Enhancers	Primary hematopoietic stem cells	blood
12	chr7:149671600-149672200	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr7:149671600-149672400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:149672000-149672400	Enhancers	H1 Cell Line	embryonic stem cell
15	chr7:149672000-149672400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr7:149672000-149673000	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr7:149672200-149672400	Active TSS	HUES48 Cell Line	embryonic stem cell
18	chr7:149672200-149672400	Enhancers	Duodenum Mucosa	Duodenum
19	chr7:149672200-149672800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr7:149672200-149673200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr7:149672200-149673200	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr7:149672200-149673200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:149672400-149672800	Active TSS	H1 Cell Line	embryonic stem cell
24	chr7:149672400-149672800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr7:149672400-149673200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr7:149672400-149673200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr7:149672400-149673200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr7:149672600-149673000	Active TSS	Primary hematopoietic stem cells	blood
29	chr7:149672800-149673200	Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr7:149672800-149673200	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr7:149673200-149676000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr7:149676000-149676400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr7:149688400-149688600	Enhancers	Gastric	stomach
34	chr7:149688600-149688800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr7:149688600-149696000	Weak transcription	Gastric	stomach
36	chr7:149689200-149690000	Enhancers	Pancreas	Pancrea
37	chr7:149689200-149690000	Bivalent Enhancer	Stomach Mucosa	stomach
38	chr7:149692000-149700600	Weak transcription	Right Atrium	heart
39	chr7:149692400-149692600	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr7:149692600-149700400	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr7:149692800-149693000	Enhancers	Brain Angular Gyrus	brain
42	chr7:149693000-149700400	Weak transcription	Brain Angular Gyrus	brain
43	chr7:149694800-149700200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr7:149694800-149700400	Weak transcription	Ovary	ovary
45	chr7:149696000-149696200	Enhancers	Brain Anterior Caudate	brain
46	chr7:149696000-149696600	Enhancers	Gastric	stomach
47	chr7:149696200-149698000	Weak transcription	Pancreas	Pancrea
48	chr7:149696200-149700400	Weak transcription	Brain Anterior Caudate	brain
49	chr7:149696600-149700400	Weak transcription	Gastric	stomach
50	chr7:149697800-149698600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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