Variant report

Variant	nsv1028636
Chromosome Location	chr7:125073718-125406148
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1054)
CpG islands
(count:0)
Chromatin interactive
region (count:71)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1054 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:125245371-125245822	K562	blood:	n/a	n/a
2	ARID3A	chr7:125235405-125235419	K562	blood:	n/a	n/a
3	ARID3A	chr7:125207883-125208163	K562	blood:	n/a	n/a
4	ARID3A	chr7:125112702-125112705	K562	blood:	n/a	n/a
5	ARID3A	chr7:125238528-125238531	K562	blood:	n/a	n/a
6	ARID3A	chr7:125145112-125145113	K562	blood:	n/a	n/a
7	ATF1	chr7:125099017-125099154	K562	blood:	n/a	n/a
8	ATF1	chr7:125155568-125155672	K562	blood:	n/a	n/a
9	ATF1	chr7:125304902-125304935	K562	blood:	n/a	n/a
10	ATF1	chr7:125102482-125102530	K562	blood:	n/a	n/a
11	ATF2	chr7:125208800-125209277	GM12878	blood:	n/a	n/a
12	ATF2	chr7:125292085-125292579	GM12878	blood:	n/a	n/a
13	ATF2	chr7:125208736-125209317	GM12878	blood:	n/a	n/a
14	ATF3	chr7:125245272-125245589	K562	blood:	n/a	n/a
15	BACH1	chr7:125144864-125145256	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr7:125144988-125145184	K562	blood:	n/a	n/a
17	BACH1	chr7:125250853-125250856	K562	blood:	n/a	n/a
18	BACH1	chr7:125245462-125245548	H1-hESC	embryonic stem cell:	n/a	chr7:125245471-125245485
19	BATF	chr7:125131056-125131238	GM12878	blood:	n/a	n/a
20	BATF	chr7:125208879-125209269	GM12878	blood:	n/a	n/a
21	BATF	chr7:125400561-125400782	GM12878	blood:	n/a	n/a
22	BATF	chr7:125208852-125209217	GM12878	blood:	n/a	n/a
23	BATF	chr7:125144978-125145174	GM12878	blood:	n/a	chr7:125145074-125145085
24	BCL11A	chr7:125208927-125209202	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:125208879-125209307	GM12878	blood:	n/a	n/a
26	BCL3	chr7:125292138-125292574	GM12878	blood:	n/a	n/a
27	BCL3	chr7:125208897-125209206	GM12878	blood:	n/a	n/a
28	BCLAF1	chr7:125208875-125209224	GM12878	blood:	n/a	n/a
29	BCLAF1	chr7:125208811-125209257	GM12878	blood:	n/a	n/a
30	BHLHE40	chr7:125301808-125302109	K562	blood:	n/a	n/a
31	BHLHE40	chr7:125178945-125179203	K562	blood:	n/a	chr7:125179077-125179098 chr7:125179081-125179094
32	BHLHE40	chr7:125375284-125375348	K562	blood:	n/a	n/a
33	BHLHE40	chr7:125201165-125201410	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:125208861-125209208	GM12878	blood:	n/a	n/a
35	BHLHE40	chr7:125242283-125242313	K562	blood:	n/a	n/a
36	BHLHE40	chr7:125315765-125315880	K562	blood:	n/a	n/a
37	BRCA1	chr7:125131722-125131738	GM12878	blood:	n/a	n/a
38	BRCA1	chr7:125311175-125311315	H1-hESC	embryonic stem cell:	n/a	n/a
39	CBX3	chr7:125099171-125099452	K562	blood:	n/a	n/a
40	CBX3	chr7:125204088-125204395	K562	blood:	n/a	n/a
41	CBX3	chr7:125377948-125378165	K562	blood:	n/a	n/a
42	CBX3	chr7:125377833-125378215	K562	blood:	n/a	n/a
43	CBX3	chr7:125099156-125099430	K562	blood:	n/a	n/a
44	CBX3	chr7:125301630-125302099	K562	blood:	n/a	n/a
45	CCNT2	chr7:125245371-125245832	K562	blood:	n/a	n/a
46	CCNT2	chr7:125301701-125301994	K562	blood:	n/a	n/a
47	CEBPB	chr7:125099121-125099384	IMR90	lung:	n/a	chr7:125099255-125099266
48	CEBPB	chr7:125192461-125192716	A549	lung:	n/a	chr7:125192548-125192559
49	CEBPB	chr7:125144418-125144733	K562	blood:	n/a	n/a
50	CEBPB	chr7:125162115-125162309	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:125205327..125207901-chr7:125208820..125211664,2	K562	blood:
2	chr7:125251686..125253446-chr7:125261235..125263882,2	K562	blood:
3	chr7:125203772..125205320-chr7:125225530..125228131,2	K562	blood:
4	chr7:125125355..125128224-chr7:125131443..125135163,4	K562	blood:
5	chr7:125190321..125191930-chr7:125194449..125196273,2	K562	blood:
6	chr7:125226088..125228401-chr7:125230345..125233728,3	K562	blood:
7	chr7:125391124..125394118-chr7:125397604..125400061,2	K562	blood:
8	chr7:125385463..125387105-chr7:125388625..125390168,2	K562	blood:
9	chr7:125089598..125092751-chr7:125096828..125101024,3	K562	blood:
10	chr7:124846681..124848535-chr7:125206338..125208006,2	K562	blood:
11	chr7:125369632..125371193-chr7:125372789..125375510,2	K562	blood:
12	chr7:125234853..125237677-chr7:125237685..125240938,4	K562	blood:
13	chr7:125108997..125111782-chr7:125114989..125116888,2	K562	blood:
14	chr7:125023517..125024026-chr7:125310752..125311652,2	MCF-7	breast:
15	chr7:125203772..125205320-chr7:125225530..125228131,2	K562	blood:
16	chr7:125251686..125253446-chr7:125261235..125263882,2	K562	blood:
17	chr7:125310080..125313010-chr7:125315945..125318441,2	K562	blood:
18	chr7:125338629..125340672-chr7:125343129..125344648,2	K562	blood:
19	chr7:125243932..125247685-chr7:125249366..125252787,4	K562	blood:
20	chr7:125266350..125268456-chr7:125268990..125271512,2	K562	blood:
21	chr7:125391124..125394118-chr7:125397604..125400061,2	K562	blood:
22	chr7:125204110..125205826-chr7:125284105..125286281,2	K562	blood:
23	chr7:125126724..125128959-chr7:125132341..125134111,2	K562	blood:
24	chr7:125108997..125111782-chr7:125114989..125116888,2	K562	blood:
25	chr7:125218658..125220340-chr7:125222287..125223970,2	K562	blood:
26	chr7:125325822..125328394-chr7:125330208..125331998,2	K562	blood:
27	chr7:125234853..125237677-chr7:125237685..125240938,4	K562	blood:
28	chr7:125325822..125328394-chr7:125330208..125331998,2	K562	blood:
29	chr7:125070959..125073239-chr7:125075739..125078658,3	K562	blood:
30	chr7:125280203..125282931-chr7:125290069..125292178,2	K562	blood:
31	chr7:125269070..125270794-chr7:125275616..125278202,2	K562	blood:
32	chr7:125384743..125387377-chr7:125395816..125398229,2	K562	blood:
33	chr7:125089598..125092751-chr7:125096828..125101024,3	K562	blood:
34	chr7:125241383..125243841-chr7:125245305..125247119,2	K562	blood:
35	chr7:124699671..124700472-chr7:125310284..125311293,4	MCF-7	breast:
36	chr7:125280203..125282931-chr7:125290069..125292178,2	K562	blood:
37	chr7:125310080..125313010-chr7:125315945..125318441,2	K562	blood:
38	chr7:125226088..125228401-chr7:125230345..125233728,3	K562	blood:
39	chr7:125172761..125175135-chr7:125186431..125188601,2	K562	blood:
40	chr7:125172761..125175135-chr7:125186431..125188601,2	K562	blood:
41	chr7:125385605..125387936-chr7:125388625..125390972,2	K562	blood:
42	chr7:125218658..125220340-chr7:125222287..125223970,2	K562	blood:
43	chr7:125241383..125243591-chr7:125245619..125247438,2	K562	blood:
44	chr7:125385463..125387105-chr7:125388625..125390168,2	K562	blood:
45	chr7:125083153..125085780-chr7:125088082..125089929,2	K562	blood:
46	chr7:125392984..125395323-chr7:125485232..125486912,2	K562	blood:
47	chr7:125266350..125268456-chr7:125268990..125271512,2	K562	blood:
48	chr7:125126724..125128959-chr7:125132341..125134111,2	K562	blood:
49	chr7:125271199..125273030-chr7:125279444..125281182,2	K562	blood:
50	chr7:125234594..125236456-chr7:125238613..125240921,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAM1-6	chr7:125101535-125101923	ENSG00000227869
2	lnc-SPAM1-6	chr7:125101535-125101704	ENSG00000227869
3	lnc-SPAM1-6	chr7:125101535-125101665	ENSG00000227869
4	lnc-SPAM1-6	chr7:125078165-125078351	NONHSAT123109
5	lnc-SPAM1-6	chr7:125078276-125078351	ENSG00000227869
6	lnc-SPAM1-6	chr7:125101535-125101923	NONHSAT123109
7	lnc-SPAM1-6	chr7:125078165-125078351	ENSG00000227869
8	lnc-SPAM1-6	chr7:125106324-125106455	NONHSAT123109
9	lnc-SPAM1-6	chr7:125078199-125078351	ENSG00000227869
10	lnc-SPAM1-6	chr7:125106324-125106455	ENSG00000227869

No data

Variant related genes	Relation type
ENSG00000227869	TF binding region
ENSG00000227869	chromatin interactions

Extended variants
information (count: 4078 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4078 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541888511	chr7:125073718-125073719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs6957629	chr7:125073725-125073726	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs6977802	chr7:125073728-125073729	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs556880478	chr7:125073760-125073761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs573595509	chr7:125073762-125073763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541000086	chr7:125073802-125073803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560770423	chr7:125073894-125073895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150104189	chr7:125073896-125073897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542442609	chr7:125073930-125073931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552541545	chr7:125073950-125073951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs76914142	chr7:125074017-125074018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs367602482	chr7:125074021-125074022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201950079	chr7:125074120-125074121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74595963	chr7:125074121-125074122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539131643	chr7:125074146-125074147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138384169	chr7:125074205-125074206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568185067	chr7:125074221-125074222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs17132915	chr7:125074269-125074270	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs547350257	chr7:125074286-125074287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570700455	chr7:125074289-125074290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78086468	chr7:125074295-125074296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs17148380	chr7:125074333-125074334	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs185548522	chr7:125074356-125074357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535610968	chr7:125074411-125074412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555524230	chr7:125074441-125074442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190755554	chr7:125074455-125074456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375091412	chr7:125074458-125074459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181551697	chr7:125074509-125074510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557783499	chr7:125074531-125074532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs61523868	chr7:125074546-125074547	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs189168810	chr7:125074590-125074591	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs149257578	chr7:125074591-125074592	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs531952095	chr7:125074597-125074598	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs73448715	chr7:125074624-125074625	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs143440979	chr7:125074677-125074678	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs532285790	chr7:125074715-125074716	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs181108573	chr7:125074780-125074781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9691894	chr7:125074796-125074797	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs73448717	chr7:125074819-125074820	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs533111100	chr7:125074836-125074837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185850105	chr7:125074855-125074856	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs190760176	chr7:125074871-125074872	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs1896470	chr7:125074911-125074912	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs555561034	chr7:125074915-125074916	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs565826391	chr7:125074941-125074942	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs534685152	chr7:125074968-125074969	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs143709531	chr7:125074973-125074974	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs577580329	chr7:125075000-125075001	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs543020850	chr7:125075037-125075038	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs75550883	chr7:125075050-125075051	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Autism	20858243	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:125065800-125078000	Weak transcription	HMEC	breast
2	chr7:125068200-125086200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:125078000-125078200	Enhancers	HMEC	breast
4	chr7:125084800-125085000	Bivalent Enhancer	Fetal Lung	lung
5	chr7:125085000-125087000	Enhancers	Fetal Lung	lung
6	chr7:125086200-125086800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:125100200-125100400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr7:125100400-125101400	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr7:125100800-125102200	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr7:125101400-125102200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr7:125102200-125102800	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr7:125102800-125103000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr7:125106200-125108400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:125108400-125109000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr7:125129000-125131200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:125129200-125129600	Enhancers	Brain Substantia Nigra	brain
17	chr7:125129200-125130000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr7:125129200-125130000	Enhancers	Brain Hippocampus Middle	brain
19	chr7:125129800-125130200	Enhancers	Fetal Brain Male	brain
20	chr7:125143200-125147200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:125143800-125144000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr7:125143800-125145200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:125144000-125144600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr7:125144000-125145000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr7:125144200-125146800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr7:125144600-125146400	Enhancers	K562	blood
27	chr7:125144600-125146600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr7:125144600-125146600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr7:125144600-125147000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr7:125144600-125147200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr7:125144800-125145200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr7:125144800-125146600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr7:125145000-125145400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr7:125145000-125145400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:125145000-125146000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr7:125145000-125146400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr7:125145000-125146600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr7:125145000-125146600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr7:125145000-125146800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr7:125145200-125145600	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr7:125145400-125145800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr7:125145400-125146600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:125145600-125146800	Enhancers	H1 Cell Line	embryonic stem cell
44	chr7:125145800-125146600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr7:125145800-125146800	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr7:125146200-125146600	Enhancers	Fetal Muscle Leg	muscle
47	chr7:125150200-125150600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr7:125150400-125152200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr7:125150600-125151600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr7:125151400-125152000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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