Variant report

Variant	nsv889437
Chromosome Location	chr7:149610781-149786096
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	chr7:149742080-149742094	K562	blood:	n/a	n/a
2	ATF1	chr7:149700297-149700734	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	BATF	chr7:149618320-149618563	GM12878	blood:	n/a	n/a
8	BCL3	chr7:149631103-149631404	GM12878	blood:	n/a	n/a
9	BCL3	chr7:149630950-149631218	GM12878	blood:	n/a	n/a
10	CEBPB	chr7:149684147-149684317	H1-hESC	embryonic stem cell:	n/a	chr7:149684215-149684232
11	CEBPB	chr7:149701346-149701464	A549	lung:	n/a	n/a
12	CEBPB	chr7:149713771-149714042	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:149615029-149615227	HepG2	liver:	n/a	chr7:149615084-149615093 chr7:149615082-149615095 chr7:149615084-149615093 chr7:149615084-149615093 chr7:149615083-149615094 chr7:149615084-149615093 chr7:149615082-149615095 chr7:149615082-149615093
14	CEBPB	chr7:149701451-149701643	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:149667593-149667795	HepG2	liver:	n/a	chr7:149667743-149667754
16	CEBPB	chr7:149784693-149784950	HepG2	liver:	n/a	chr7:149784796-149784807
17	CEBPB	chr7:149701434-149701491	K562	blood:	n/a	n/a
18	CEBPB	chr7:149684039-149684320	K562	blood:	n/a	chr7:149684215-149684232
19	CEBPB	chr7:149684112-149684277	K562	blood:	n/a	chr7:149684215-149684232
20	CEBPB	chr7:149667610-149667796	K562	blood:	n/a	chr7:149667743-149667754
21	CEBPB	chr7:149667622-149667822	IMR90	lung:	n/a	chr7:149667743-149667754
22	CEBPB	chr7:149615022-149615152	A549	lung:	n/a	chr7:149615084-149615093 chr7:149615082-149615095 chr7:149615084-149615093 chr7:149615084-149615093 chr7:149615083-149615094 chr7:149615084-149615093 chr7:149615082-149615095 chr7:149615082-149615093
23	CEBPB	chr7:149615022-149615161	K562	blood:	n/a	chr7:149615084-149615093 chr7:149615082-149615095 chr7:149615084-149615093 chr7:149615084-149615093 chr7:149615083-149615094 chr7:149615084-149615093 chr7:149615082-149615095 chr7:149615082-149615093
24	CHD1	chr7:149746398-149746684	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr7:149746382-149746488	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr7:149742790-149743004	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr7:149781999-149782045	HepG2	liver:	n/a	n/a
28	CTCF	chr7:149746049-149746383	MCF-7	breast:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
29	CTCF	chr7:149742754-149743021	K562	blood:	n/a	n/a
30	CTCF	chr7:149757673-149757927	Lung_OC	lung:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
31	CTCF	chr7:149746076-149746348	GM19238	blood:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
32	CTCF	chr7:149742800-149742950	K562	blood:	n/a	n/a
33	CTCF	chr7:149661110-149661349	K562	blood:	n/a	chr7:149661275-149661284 chr7:149661269-149661287
34	CTCF	chr7:149698460-149698610	HEK293	kidney:	n/a	n/a
35	CTCF	chr7:149722270-149722485	LNCaP	prostate:	n/a	chr7:149722360-149722381 chr7:149722365-149722383
36	CTCF	chr7:149757533-149757908	K562	blood:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
37	CTCF	chr7:149757620-149757770	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr7:149746200-149746350	HUVEC	blood vessel:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
39	CTCF	chr7:149644495-149644745	K562	blood:	n/a	chr7:149644582-149644595
40	CTCF	chr7:149722359-149722388	MCF-7	breast:	n/a	chr7:149722360-149722381 chr7:149722365-149722383
41	CTCF	chr7:149731012-149731132	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr7:149744379-149744387	GM10266	blood:	n/a	n/a
43	CTCF	chr7:149781700-149781850	K562	blood:	n/a	n/a
44	CTCF	chr7:149742780-149742930	GM12864	blood:	n/a	n/a
45	CTCF	chr7:149742680-149742970	NHLF	lung:	n/a	n/a
46	CTCF	chr7:149757660-149757810	GM12865	blood:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
47	CTCF	chr7:149746082-149746379	Medullo	brain:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
48	CTCF	chr7:149781966-149781970	HepG2	liver:	n/a	n/a
49	CTCF	chr7:149745920-149746070	HepG2	liver:	n/a	n/a
50	CTCF	chr7:149757620-149757770	AG09319	gingival:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:149746077-149746127	HMEC	breast:	n/a
2	chr7:149749941-149749991	CMK	blood:	n/a
3	chr7:149746077-149746127	HMEC	breast:	n/a
4	chr7:149749941-149749991	CMK	blood:	n/a
5	chr7:149746640-149746690	NHDF-neo	bronchial:	n/a
6	chr7:149749941-149749991	HCM	heart:	n/a
7	chr7:149749941-149749991	GM12892	blood:	n/a
8	chr7:149780548-149780598	AG04450	lung:	fetal
9	chr7:149746640-149746690	AG10803	skin:	n/a
10	chr7:149744597-149744647	ovcar-3	ovarian:	n/a
11	chr7:149767828-149767878	NHDF-neo	bronchial:	n/a
12	chr7:149738473-149738523	PrEC	prostate:	n/a
13	chr7:149738473-149738523	SK-N-SH	brain:	n/a
14	chr7:149744935-149744985	GM12878	blood:	n/a
15	chr7:149744597-149744647	AG09309	skin:	n/a
16	chr7:149744041-149744091	NH-A	brain:	n/a
17	chr7:149733103-149733153	GM12891	blood:	n/a
18	chr7:149732847-149732897	CMK	blood:	n/a
19	chr7:149735729-149735779	HEEpiC	esophagus:	n/a
20	chr7:149745299-149745349	SAEC	small airway:	n/a
21	chr7:149780548-149780598	IMR90	lung:	fetal
22	chr7:149746468-149746518	HAEpiC	amniotic membrane:	n/a
23	chr7:149738501-149738551	U87	brain:	n/a
24	chr7:149767828-149767878	SAEC	small airway:	n/a
25	chr7:149642580-149642630	K562	blood:	n/a
26	chr7:149767502-149767552	Hela-S3	cervix:	n/a
27	chr7:149738501-149738551	NB4	blood:	n/a
28	chr7:149780548-149780598	HCT-116	colon:	n/a
29	chr7:149735729-149735779	NT2-D1	testis:	n/a
30	chr7:149731767-149731817	HRE	kidney:	n/a
31	chr7:149742121-149742171	MCF-7	breast:	n/a
32	chr7:149738473-149738523	NT2-D1	testis:	n/a
33	chr7:149642580-149642630	MCF-7	breast:	n/a
34	chr7:149731742-149731792	NB4	blood:	n/a
35	chr7:149767502-149767552	SK-N-MC	brain:	n/a
36	chr7:149745299-149745349	HPAEpiC	pulmonary alveolar:	n/a
37	chr7:149746468-149746518	NH-A	brain:	n/a
38	chr7:149732579-149732629	Hepatocyte	liver:	n/a
39	chr7:149732847-149732897	SAEC	small airway:	n/a
40	chr7:149746640-149746690	HCT-116	colon:	n/a
41	chr7:149731767-149731817	HRCEpiC	kidney:	n/a
42	chr7:149736127-149736177	CMK	blood:	n/a
43	chr7:149733103-149733153	PANC-1	pancreas:	n/a
44	chr7:149732579-149732629	BJ	skin:	n/a
45	chr7:149749941-149749991	HAEpiC	amniotic membrane:	n/a
46	chr7:149744935-149744985	GM19239	blood:	n/a
47	chr7:149736127-149736177	AG10803	skin:	n/a
48	chr7:149736127-149736177	PrEC	prostate:	n/a
49	chr7:149744041-149744091	HRCEpiC	kidney:	n/a
50	chr7:149732847-149732897	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:149699024..149700856-chr7:153788710..153791500,2	K562	blood:
2	chr7:149580322..149580844-chr7:149745955..149746566,2	MCF-7	breast:
3	chr7:149757556..149758057-chr7:149919306..149919858,2	MCF-7	breast:
4	chr7:149639335..149639849-chr7:153850966..153851836,2	MCF-7	breast:

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

Variant related genes	Relation type
ENSG00000241449	TF binding region
ENSG00000224016	TF binding region
ENSG00000260555	TF binding region
ENSG00000241449	CpG island
ENSG00000224016	CpG island
ENSG00000260555	CpG island
SOCS2	miRNA target sites
JPH1	miRNA target sites

Extended variants
information (count: 5213 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:5213 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191809196	chr7:149623426-149623427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140728607	chr7:149623437-149623438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372804344	chr7:149623460-149623461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183480882	chr7:149623475-149623476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551637561	chr7:149623492-149623493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187551941	chr7:149623517-149623518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537707406	chr7:149623518-149623519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138218624	chr7:149623556-149623557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2969809	chr7:149623565-149623566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567300542	chr7:149623570-149623571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536253984	chr7:149623574-149623575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2969810	chr7:149623588-149623589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553110002	chr7:149623616-149623617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142850167	chr7:149623626-149623627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4725844	chr7:149623633-149623634	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs192595121	chr7:149623650-149623651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182095354	chr7:149623651-149623652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2449719	chr7:149623665-149623666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565043659	chr7:149623699-149623700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560845473	chr7:149623721-149623722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529289045	chr7:149623730-149623731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532258625	chr7:149623745-149623746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs62490831	chr7:149623753-149623754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186607256	chr7:149623776-149623777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192431427	chr7:149623799-149623800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551969148	chr7:149623828-149623829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547471674	chr7:149623917-149623918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559301362	chr7:149623950-149623951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565375730	chr7:149623953-149623954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531107684	chr7:149623968-149623969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551345141	chr7:149623998-149623999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs567953192	chr7:149624042-149624043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184869852	chr7:149624140-149624141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143837999	chr7:149624154-149624155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141788135	chr7:149624165-149624166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140730827	chr7:149624166-149624167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs377690581	chr7:149624210-149624211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536254120	chr7:149624246-149624247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2462117	chr7:149624264-149624265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs6953393	chr7:149624289-149624290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2969811	chr7:149624358-149624359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2969812	chr7:149624364-149624365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2969824	chr7:149627423-149627424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144491005	chr7:149627427-149627428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs80198655	chr7:149627510-149627511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs141452976	chr7:149627578-149627579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369210774	chr7:149627596-149627597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149763379	chr7:149627601-149627602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs568483711	chr7:149627602-149627603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376239539	chr7:149627657-149627658	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
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:649 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:149623400-149623800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:149623600-149624400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr7:149627400-149627600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:149627600-149627800	Enhancers	Placenta	Placenta
5	chr7:149642400-149642600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:149644800-149645000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr7:149644800-149645000	Enhancers	Fetal Muscle Trunk	muscle
8	chr7:149644800-149645000	Enhancers	Fetal Muscle Leg	muscle
9	chr7:149644800-149645200	Enhancers	Left Ventricle	heart
10	chr7:149644800-149645400	Enhancers	Fetal Brain Male	brain
11	chr7:149644800-149645600	Enhancers	Right Atrium	heart
12	chr7:149644800-149645800	Enhancers	HSMMtube	muscle
13	chr7:149645000-149645800	Weak transcription	Fetal Muscle Trunk	muscle
14	chr7:149645000-149645800	Weak transcription	Fetal Muscle Leg	muscle
15	chr7:149645800-149646000	Enhancers	Fetal Muscle Trunk	muscle
16	chr7:149645800-149646800	Enhancers	Fetal Muscle Leg	muscle
17	chr7:149645800-149647200	Weak transcription	HSMMtube	muscle
18	chr7:149645800-149647800	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr7:149646000-149647200	Weak transcription	Fetal Muscle Trunk	muscle
20	chr7:149646200-149647800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr7:149646200-149649000	Enhancers	Dnd41	blood
22	chr7:149646400-149646600	Enhancers	Primary hematopoietic stem cells	blood
23	chr7:149646400-149646800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr7:149646400-149647400	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr7:149646400-149647400	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr7:149646400-149647400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr7:149646400-149647400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr7:149646400-149647600	Enhancers	Primary T cells fromperipheralblood	blood
29	chr7:149646400-149647600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr7:149646600-149647200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr7:149646600-149647400	Enhancers	Primary B cells from cord blood	blood
32	chr7:149646600-149647400	Weak transcription	Primary hematopoietic stem cells	blood
33	chr7:149646600-149647600	Enhancers	Primary B cells from peripheral blood	blood
34	chr7:149646600-149647600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr7:149646600-149647600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr7:149646600-149647600	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr7:149646600-149647800	Enhancers	Fetal Thymus	thymus
38	chr7:149647200-149647400	Enhancers	Primary T cells from cord blood	blood
39	chr7:149647200-149647400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr7:149647200-149647400	Enhancers	Fetal Muscle Trunk	muscle
41	chr7:149647200-149647600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:149647200-149647600	Enhancers	GM12878-XiMat	blood
43	chr7:149647200-149647600	Enhancers	HSMMtube	muscle
44	chr7:149647400-149647600	Enhancers	Primary hematopoietic stem cells	blood
45	chr7:149647400-149648400	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr7:149647400-149648400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr7:149647400-149657800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr7:149647600-149647800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:149647600-149648400	Weak transcription	Primary hematopoietic stem cells	blood
50	chr7:149647600-149648400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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