Variant report

Variant	nsv888619
Chromosome Location	chr7:83452312-83549032
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	BCLAF1	chr7:83466984-83467316	GM12878	blood:	n/a	chr7:83467258-83467267
2	BRCA1	chr7:83504213-83504299	GM12878	blood:	n/a	n/a
3	CEBPB	chr7:83535573-83535698	HepG2	liver:	n/a	chr7:83535595-83535606
4	CEBPB	chr7:83509713-83509971	HepG2	liver:	n/a	chr7:83509817-83509828 chr7:83509815-83509828 chr7:83509868-83509881 chr7:83509830-83509841 chr7:83509868-83509879 chr7:83509815-83509826 chr7:83509830-83509843 chr7:83509815-83509828 chr7:83509817-83509828
5	CEBPB	chr7:83495922-83496303	Hela-S3	cervix:	n/a	chr7:83496064-83496081
6	CEBPB	chr7:83495838-83496333	HCT-116	colon:	n/a	chr7:83496064-83496081
7	CEBPB	chr7:83495886-83496333	HCT-116	colon:	n/a	chr7:83496064-83496081
8	CEBPB	chr7:83502416-83502584	HepG2	liver:	n/a	chr7:83502451-83502462
9	CEBPB	chr7:83509715-83509983	Hela-S3	cervix:	n/a	chr7:83509817-83509828 chr7:83509815-83509828 chr7:83509868-83509881 chr7:83509830-83509841 chr7:83509868-83509879 chr7:83509815-83509826 chr7:83509830-83509843 chr7:83509815-83509828 chr7:83509817-83509828
10	CEBPB	chr7:83540680-83540974	K562	blood:	n/a	chr7:83540811-83540822 chr7:83540809-83540822 chr7:83540809-83540822
11	CHD2	chr7:83506023-83506052	GM12878	blood:	n/a	n/a
12	CTCF	chr7:83462380-83462530	HMF	breast:	n/a	chr7:83462511-83462519 chr7:83462501-83462522
13	CTCF	chr7:83504180-83504330	BE2_C	brain:	n/a	n/a
14	CTCF	chr7:83472947-83472952	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr7:83529692-83529744	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr7:83472887-83472946	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr7:83462371-83462653	GM12878	blood:	n/a	chr7:83462511-83462519 chr7:83462501-83462522
18	CTCF	chr7:83504671-83504720	GM20000	blood:	n/a	n/a
19	CTCF	chr7:83472499-83472555	ProgFib	skin:	n/a	n/a
20	CTCF	chr7:83462400-83462550	GM06990	blood:	n/a	chr7:83462511-83462519 chr7:83462501-83462522
21	CTCF	chr7:83504723-83504728	GM20000	blood:	n/a	n/a
22	CTCF	chr7:83504214-83504268	Hela-S3	cervix:	n/a	n/a
23	CUX1	chr7:83467191-83467440	GM12878	blood:	n/a	n/a
24	CUX1	chr7:83464442-83464612	GM12878	blood:	n/a	n/a
25	E2F4	chr7:83459200-83459232	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr7:83465522-83465746	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr7:83482985-83483393	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr7:83548634-83548922	MCF10A-Er-Src	breast:	n/a	n/a
29	EBF1	chr7:83465525-83465672	GM12878	blood:	n/a	n/a
30	EBF1	chr7:83466922-83467282	GM12878	blood:	n/a	n/a
31	EBF1	chr7:83505934-83506282	GM12878	blood:	n/a	chr7:83506136-83506145 chr7:83506133-83506144 chr7:83506136-83506146
32	EBF1	chr7:83540260-83540267	GM12878	blood:	n/a	n/a
33	EP300	chr7:83481550-83481731	SK-N-SH_RA	brain:	n/a	n/a
34	EP300	chr7:83477868-83477972	GM12878	blood:	n/a	chr7:83477957-83477964
35	EP300	chr7:83478463-83478812	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr7:83495984-83496215	Hela-S3	cervix:	n/a	chr7:83496068-83496076
37	EP300	chr7:83478520-83478803	SK-N-SH_RA	brain:	n/a	n/a
38	EP300	chr7:83481515-83481841	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr7:83465424-83465662	GM12878	blood:	n/a	chr7:83465554-83465568
40	FAM48A	chr7:83505917-83506251	GM12878	blood:	n/a	n/a
41	FOS	chr7:83454236-83454644	HUVEC	blood vessel:	n/a	chr7:83454461-83454471 chr7:83454463-83454470 chr7:83454460-83454471 chr7:83454462-83454470 chr7:83454460-83454472
42	FOS	chr7:83505913-83506283	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr7:83453627-83453944	MCF10A-Er-Src	breast:	n/a	chr7:83453788-83453798
44	FOS	chr7:83453656-83453855	MCF10A-Er-Src	breast:	n/a	chr7:83453788-83453798
45	FOS	chr7:83505894-83506293	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr7:83453509-83454030	HUVEC	blood vessel:	n/a	chr7:83453788-83453798
47	FOS	chr7:83481518-83481892	HUVEC	blood vessel:	n/a	chr7:83481697-83481708
48	FOS	chr7:83481538-83481833	MCF10A-Er-Src	breast:	n/a	chr7:83481697-83481708
49	FOS	chr7:83505908-83506283	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr7:83478672-83478701	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:83479479-83479529	Hela-S3	cervix:	n/a
2	chr7:83461505-83461555	Jurkat	blood:	n/a
3	chr7:83479479-83479529	SK-N-SH_RA	brain:	n/a
4	chr7:83479479-83479529	K562	blood:	n/a
5	chr7:83479479-83479529	BE2_C	brain:	n/a
6	chr7:83461505-83461555	SAEC	small airway:	n/a
7	chr7:83479479-83479529	HAEpiC	amniotic membrane:	n/a
8	chr7:83461505-83461555	BJ	skin:	n/a
9	chr7:83461505-83461555	GM12891	blood:	n/a
10	chr7:83461505-83461555	AG04449	skin:	fetal
11	chr7:83479479-83479529	CMK	blood:	n/a
12	chr7:83479479-83479529	HepG2	liver:	n/a
13	chr7:83461505-83461555	HCT-116	colon:	n/a
14	chr7:83479479-83479529	GM06990	blood:	n/a
15	chr7:83461505-83461555	A549	lung:	n/a
16	chr7:83461505-83461555	K562	blood:	n/a
17	chr7:83479479-83479529	MCF-7	breast:	n/a
18	chr7:83479479-83479529	SAEC	small airway:	n/a
19	chr7:83479479-83479529	MCF10A-Er-Src	breast:	n/a
20	chr7:83479479-83479529	RPTEC	kidney:	n/a
21	chr7:83479479-83479529	U87	brain:	n/a
22	chr7:83479479-83479529	ECC-1	luminal epithelium:	n/a
23	chr7:83461505-83461555	T-47D	breast:	n/a
24	chr7:83479479-83479529	HCPEpiC	choroid plexus:	n/a
25	chr7:83479479-83479529	Jurkat	blood:	n/a
26	chr7:83479479-83479529	HNPCEpiC	eye:	n/a
27	chr7:83461505-83461555	CMK	blood:	n/a
28	chr7:83479479-83479529	GM19239	blood:	n/a
29	chr7:83461505-83461555	SKMC	muscle:	n/a
30	chr7:83479479-83479529	Hepatocyte	liver:	n/a
31	chr7:83479479-83479529	IMR90	lung:	fetal
32	chr7:83479479-83479529	NHBE	bronchial:	n/a
33	chr7:83461505-83461555	HAEpiC	amniotic membrane:	n/a
34	chr7:83479479-83479529	HEK293	kidney:	embryo
35	chr7:83461505-83461555	U87	brain:	n/a
36	chr7:83461505-83461555	HRE	kidney:	n/a
37	chr7:83461505-83461555	SK-N-SH_RA	brain:	n/a
38	chr7:83479479-83479529	HIPEpiC	eye:	n/a
39	chr7:83479479-83479529	AG10803	skin:	n/a
40	chr7:83461505-83461555	HIPEpiC	eye:	n/a
41	chr7:83461505-83461555	MCF-7	breast:	n/a
42	chr7:83479479-83479529	HRPEpiC	eye:	n/a
43	chr7:83479479-83479529	HCT-116	colon:	n/a
44	chr7:83479479-83479529	H1-hESC	embryonic stem cell:	embryo
45	chr7:83479479-83479529	GM12878	blood:	n/a
46	chr7:83479479-83479529	ovcar-3	ovarian:	n/a
47	chr7:83479479-83479529	SKMC	muscle:	n/a
48	chr7:83461505-83461555	AG09319	gingival:	n/a
49	chr7:83479479-83479529	SK-N-MC	brain:	n/a
50	chr7:83461505-83461555	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:83460398..83462244-chr7:83469602..83471375,2	MCF-7	breast:
2	chr7:83456371..83459960-chr7:83460800..83464283,4	K562	blood:
3	chr7:83489185..83491209-chr7:83492617..83495468,2	MCF-7	breast:
4	chr7:83456371..83458031-chr7:83460982..83463180,2	K562	blood:
5	chr7:83541356..83543273-chr7:83544365..83547061,2	K562	blood:
6	chr7:83541356..83543273-chr7:83544365..83547061,2	K562	blood:
7	chr7:83544092..83546741-chr7:83548578..83551192,2	K562	blood:
8	chr7:83483719..83485760-chr7:83487452..83489726,2	K562	blood:
9	chr7:83489185..83491209-chr7:83492617..83495468,2	MCF-7	breast:
10	chr7:83483719..83485760-chr7:83487452..83489726,2	K562	blood:
11	chr7:83456371..83459960-chr7:83460800..83464283,4	K562	blood:
12	chr7:83456371..83458031-chr7:83460982..83463180,2	K562	blood:
13	chr7:83460398..83462244-chr7:83469602..83471375,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000222994	TF binding region
ENSG00000222994	CpG island
ENSG00000222994	chromatin interactions

Extended variants
information (count: 1863 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1863 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76764013	chr7:83452829-83452830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs80238788	chr7:83452843-83452844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192908276	chr7:83452846-83452847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559671580	chr7:83452852-83452853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80153615	chr7:83452908-83452909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551813303	chr7:83452913-83452914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11971246	chr7:83453000-83453001	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs537590810	chr7:83453066-83453067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549590899	chr7:83453087-83453088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567894347	chr7:83453099-83453100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535308106	chr7:83453133-83453134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553414497	chr7:83453134-83453135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs78033872	chr7:83453147-83453148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539063330	chr7:83453157-83453158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114362776	chr7:83453174-83453175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575720223	chr7:83453192-83453193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543146114	chr7:83453209-83453210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs143053344	chr7:83453246-83453247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573522601	chr7:83453251-83453252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571637474	chr7:83453257-83453258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532526269	chr7:83453266-83453267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75703840	chr7:83453302-83453303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs151172627	chr7:83453351-83453352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563715154	chr7:83453361-83453362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140240815	chr7:83453362-83453363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527714198	chr7:83453425-83453426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547681709	chr7:83453445-83453446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567835213	chr7:83453460-83453461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528698193	chr7:83453493-83453494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs183253648	chr7:83453518-83453519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544154481	chr7:83453541-83453542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114086746	chr7:83453542-83453543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542839916	chr7:83453544-83453545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528974111	chr7:83453621-83453622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146763104	chr7:83453674-83453675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139274429	chr7:83453702-83453703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536719140	chr7:83453706-83453707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187313023	chr7:83453720-83453721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs73390507	chr7:83453768-83453769	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs540872297	chr7:83453769-83453770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191356002	chr7:83453779-83453780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577851943	chr7:83453811-83453812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143300628	chr7:83453878-83453879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563653866	chr7:83453898-83453899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs77949374	chr7:83453981-83453982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183889896	chr7:83454042-83454043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs543113142	chr7:83454056-83454057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs561368616	chr7:83454064-83454065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186861113	chr7:83454089-83454090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs73711912	chr7:83454138-83454139	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:219 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:83452800-83454400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr7:83453200-83454600	Enhancers	Muscle Satellite Cultured Cells	--
3	chr7:83453200-83454600	Enhancers	HUVEC	blood vessel
4	chr7:83453200-83454800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr7:83453400-83453600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:83453800-83454200	Enhancers	NH-A	brain
7	chr7:83454600-83456200	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr7:83454800-83456200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr7:83455600-83457400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:83456200-83457000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr7:83456200-83457000	Enhancers	Muscle Satellite Cultured Cells	--
12	chr7:83456400-83457000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr7:83456400-83457000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr7:83459000-83459200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr7:83459000-83459200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr7:83459200-83459400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr7:83459200-83460200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr7:83459200-83460200	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr7:83459400-83460200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr7:83460200-83460400	Enhancers	H9 Cell Line	embryonic stem cell
21	chr7:83460200-83460400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:83460200-83460600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr7:83460200-83460600	ZNF genes & repeats	Aorta	Aorta
24	chr7:83460200-83460800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr7:83460200-83460800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr7:83460200-83463200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr7:83460200-83465400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr7:83460200-83465800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr7:83460400-83461400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:83460400-83461800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr7:83460400-83461800	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr7:83460400-83478800	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr7:83460600-83464000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr7:83460600-83465600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr7:83460800-83461000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr7:83460800-83461200	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr7:83460800-83461200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr7:83461000-83463400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr7:83461000-83465600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr7:83461200-83462000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr7:83461200-83464200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:83461400-83461800	Enhancers	H1 Cell Line	embryonic stem cell
43	chr7:83461400-83465000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:83461800-83462600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr7:83461800-83465400	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr7:83462000-83462400	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr7:83462400-83463400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr7:83462600-83463400	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr7:83463200-83463600	Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr7:83463400-83463800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell

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