Variant report

Variant	nsv933689
Chromosome Location	chr6:129075729-129208730
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:539)
CpG islands
(count:549)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:539 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:129204147-129204737	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr6:129075801-129076427	GM12878	blood:	n/a	n/a
3	ATF2	chr6:129075811-129076538	GM12878	blood:	n/a	n/a
4	BACH1	chr6:129169430-129169675	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:129204139-129204642	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr6:129075893-129076334	GM12878	blood:	n/a	n/a
7	BATF	chr6:129075980-129076354	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:129075961-129076334	GM12878	blood:	n/a	chr6:129076284-129076293
9	BCL11A	chr6:129075881-129076396	GM12878	blood:	n/a	chr6:129076284-129076293
10	BCL3	chr6:129075940-129076244	GM12878	blood:	n/a	n/a
11	BCLAF1	chr6:129075873-129076401	GM12878	blood:	n/a	chr6:129076284-129076293
12	BHLHE40	chr6:129075878-129076472	GM12878	blood:	n/a	n/a
13	CBX3	chr6:129162629-129163119	HCT-116	colon:	n/a	n/a
14	CBX3	chr6:129181866-129182365	HCT-116	colon:	n/a	n/a
15	CCNT2	chr6:129173362-129173718	K562	blood:	n/a	n/a
16	CCNT2	chr6:129201331-129201411	K562	blood:	n/a	n/a
17	CEBPB	chr6:129127462-129127826	HepG2	liver:	n/a	chr6:129127630-129127641
18	CEBPB	chr6:129149275-129149566	IMR90	lung:	n/a	n/a
19	CEBPB	chr6:129206905-129207227	IMR90	lung:	n/a	chr6:129207048-129207059
20	CEBPB	chr6:129206980-129207150	H1-hESC	embryonic stem cell:	n/a	chr6:129207048-129207059
21	CEBPB	chr6:129149133-129149635	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr6:129127453-129127806	IMR90	lung:	n/a	chr6:129127630-129127641
23	CEBPB	chr6:129206944-129207234	A549	lung:	n/a	chr6:129207048-129207059
24	CEBPB	chr6:129204254-129204729	H1-hESC	embryonic stem cell:	n/a	chr6:129204684-129204701
25	CEBPB	chr6:129206892-129207227	HepG2	liver:	n/a	chr6:129207048-129207059
26	CEBPB	chr6:129127478-129127811	A549	lung:	n/a	chr6:129127630-129127641
27	CEBPB	chr6:129127425-129127934	Hela-S3	cervix:	n/a	chr6:129127630-129127641
28	CEBPB	chr6:129075850-129076419	GM12878	blood:	n/a	n/a
29	CHD1	chr6:129204208-129204607	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr6:129075742-129076440	GM12878	blood:	n/a	n/a
31	CHD2	chr6:129193764-129193777	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr6:129204221-129204705	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr6:129075914-129076511	GM12878	blood:	n/a	n/a
34	CTCF	chr6:129128880-129129030	HEK293	kidney:	n/a	chr6:129128899-129128915 chr6:129128898-129128916
35	CTCF	chr6:129128840-129128997	Hela-S3	cervix:	n/a	chr6:129128899-129128915 chr6:129128898-129128916
36	CTCF	chr6:129088900-129089050	GM06990	blood:	n/a	n/a
37	CTCF	chr6:129128847-129128861	GM10266	blood:	n/a	n/a
38	CTCF	chr6:129128960-129129110	HCT-116	colon:	n/a	n/a
39	CTCF	chr6:129128960-129129110	BE2_C	brain:	n/a	n/a
40	CTCF	chr6:129128374-129129236	A549	lung:	n/a	chr6:129128899-129128915 chr6:129128898-129128916
41	CTCF	chr6:129128860-129129010	HMF	breast:	n/a	chr6:129128899-129128915 chr6:129128898-129128916
42	CTCF	chr6:129080800-129080950	HEK293	kidney:	n/a	n/a
43	CTCF	chr6:129128821-129128988	MCF-7	breast:	n/a	chr6:129128899-129128915 chr6:129128898-129128916
44	CTCF	chr6:129128860-129129010	GM12867	blood:	n/a	chr6:129128899-129128915 chr6:129128898-129128916
45	CTCF	chr6:129128820-129128970	HRPEpiC	eye:	n/a	chr6:129128899-129128915 chr6:129128898-129128916
46	CTCF	chr6:129204120-129204270	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr6:129089040-129089190	GM12872	blood:	n/a	n/a
48	CTCF	chr6:129204220-129204370	AG09319	gingival:	n/a	n/a
49	CTCF	chr6:129128860-129129010	HCT-116	colon:	n/a	chr6:129128899-129128915 chr6:129128898-129128916
50	CTCF	chr6:129204149-129204511	Fibrobl	skin:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:129204206-129204256	H1-hESC	embryonic stem cell:	embryo
2	chr6:129204339-129204389	BJ	skin:	n/a
3	chr6:129204339-129204389	T-47D	breast:	n/a
4	chr6:129204510-129204560	PrEC	prostate:	n/a
5	chr6:129203075-129203125	SK-N-SH_RA	brain:	n/a
6	chr6:129170327-129170377	HMEC	breast:	n/a
7	chr6:129170327-129170377	GM12891	blood:	n/a
8	chr6:129203075-129203125	GM06990	blood:	n/a
9	chr6:129170327-129170377	Hepatocyte	liver:	n/a
10	chr6:129170327-129170377	AG09309	skin:	n/a
11	chr6:129204125-129204175	HAEpiC	amniotic membrane:	n/a
12	chr6:129203075-129203125	RPTEC	kidney:	n/a
13	chr6:129204339-129204389	HCPEpiC	choroid plexus:	n/a
14	chr6:129204206-129204256	HEK293	kidney:	embryo
15	chr6:129203783-129203833	PFSK-1	brain:	n/a
16	chr6:129203887-129203937	SAEC	small airway:	n/a
17	chr6:129203075-129203125	BJ	skin:	n/a
18	chr6:129170327-129170377	HCT-116	colon:	n/a
19	chr6:129170327-129170377	Caco-2	colon:	n/a
20	chr6:129203887-129203937	HCT-116	colon:	n/a
21	chr6:129204510-129204560	MCF-7	breast:	n/a
22	chr6:129170327-129170377	Hela-S3	cervix:	n/a
23	chr6:129204540-129204590	T-47D	breast:	n/a
24	chr6:129204540-129204590	Hepatocyte	liver:	n/a
25	chr6:129204125-129204175	GM06990	blood:	n/a
26	chr6:129204339-129204389	GM06990	blood:	n/a
27	chr6:129204339-129204389	PFSK-1	brain:	n/a
28	chr6:129204206-129204256	HCPEpiC	choroid plexus:	n/a
29	chr6:129203887-129203937	Caco-2	colon:	n/a
30	chr6:129204125-129204175	HIPEpiC	eye:	n/a
31	chr6:129203783-129203833	ProgFib	skin:	n/a
32	chr6:129203783-129203833	CMK	blood:	n/a
33	chr6:129170327-129170377	HRPEpiC	eye:	n/a
34	chr6:129203887-129203937	HRE	kidney:	n/a
35	chr6:129203887-129203937	BE2_C	brain:	n/a
36	chr6:129203075-129203125	BE2_C	brain:	n/a
37	chr6:129204206-129204256	HAEpiC	amniotic membrane:	n/a
38	chr6:129204206-129204256	Caco-2	colon:	n/a
39	chr6:129204206-129204256	HIPEpiC	eye:	n/a
40	chr6:129203075-129203125	HMEC	breast:	n/a
41	chr6:129203075-129203125	NH-A	brain:	n/a
42	chr6:129204125-129204175	NH-A	brain:	n/a
43	chr6:129203887-129203937	NB4	blood:	n/a
44	chr6:129203075-129203125	HIPEpiC	eye:	n/a
45	chr6:129203075-129203125	T-47D	breast:	n/a
46	chr6:129204339-129204389	NT2-D1	testis:	n/a
47	chr6:129204125-129204175	PrEC	prostate:	n/a
48	chr6:129204206-129204256	NB4	blood:	n/a
49	chr6:129170327-129170377	PrEC	prostate:	n/a
50	chr6:129203887-129203937	HPAEpiC	pulmonary alveolar:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:129135147..129136858-chr6:129136884..129139829,2	MCF-7	breast:
2	chr6:129128436..129129319-chr6:129572990..129573923,5	MCF-7	breast:
3	chr17:59651616..59652970-chr6:129118414..129119434,6	MCF-7	breast:
4	chr6:129135147..129136858-chr6:129136884..129139829,2	MCF-7	breast:
5	chr6:129076919..129079735-chr6:129217747..129220615,2	K562	blood:
6	chr6:129128651..129129340-chr6:129691292..129692278,2	MCF-7	breast:
7	chr18:50436726..50437301-chr6:129203068..129203756,2	K562	blood:
8	chr6:129128405..129129261-chr6:129572586..129573739,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000202200	TF binding region
LAMA2	TF binding region
ENSG00000202200	CpG island
LAMA2	CpG island

Extended variants
information (count: 1891 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1891 , 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	rs570474872	chr6:129075774-129075775	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs537534609	chr6:129075800-129075801	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs556328635	chr6:129075815-129075816	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs574662651	chr6:129075892-129075893	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs373920273	chr6:129075919-129075920	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs535667931	chr6:129075947-129075948	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs189537151	chr6:129075954-129075955	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs370517800	chr6:129075980-129075981	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs572258579	chr6:129075989-129075990	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs7745581	chr6:129076072-129076073	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs565129188	chr6:129076114-129076115	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs139376506	chr6:129076118-129076119	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs145532347	chr6:129076141-129076142	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs376085635	chr6:129076151-129076152	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs562666153	chr6:129076180-129076181	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs374930859	chr6:129076198-129076199	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs539865081	chr6:129076201-129076202	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs140656225	chr6:129076205-129076206	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs181599980	chr6:129076206-129076207	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs548384707	chr6:129076223-129076224	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs560792041	chr6:129076236-129076237	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs7763496	chr6:129076251-129076252	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs147349277	chr6:129076303-129076304	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs10670943	chr6:129076304-129076305	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs33992254	chr6:129076305-129076306	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs57743753	chr6:129076306-129076307	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs13209291	chr6:129076335-129076336	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs186367122	chr6:129076344-129076345	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs13193353	chr6:129076382-129076383	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs570336713	chr6:129076413-129076414	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs10499139	chr6:129076415-129076416	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs542650704	chr6:129076421-129076422	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs546278484	chr6:129076435-129076436	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs13209422	chr6:129076447-129076448	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs549873572	chr6:129076456-129076457	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs72977310	chr6:129076459-129076460	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs553685295	chr6:129076513-129076514	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs17056470	chr6:129076520-129076521	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs147291886	chr6:129076521-129076522	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs191681240	chr6:129076588-129076589	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs140834816	chr6:129076591-129076592	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs544217007	chr6:129076649-129076650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs562603362	chr6:129076693-129076694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs376104082	chr6:129076703-129076704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144681647	chr6:129076708-129076709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113115512	chr6:129076745-129076746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529983813	chr6:129076768-129076769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs527920041	chr6:129076771-129076772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148928936	chr6:129076776-129076777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142240144	chr6:129076804-129076805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Neurocytoma	17123091	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Ependymoma	18628472	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21958427	CNVD
Mental retardation	17847001	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:129064400-129089200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:129074400-129078000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr6:129074600-129078000	Weak transcription	NHEK	skin
4	chr6:129075600-129075800	Active TSS	GM12878-XiMat	blood
5	chr6:129075800-129076000	Flanking Active TSS	GM12878-XiMat	blood
6	chr6:129076000-129076400	Active TSS	GM12878-XiMat	blood
7	chr6:129076400-129076600	Flanking Active TSS	GM12878-XiMat	blood
8	chr6:129076600-129077400	Enhancers	GM12878-XiMat	blood
9	chr6:129077600-129079000	Enhancers	HMEC	breast
10	chr6:129078000-129078200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr6:129078000-129081200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:129078000-129081200	Enhancers	NHEK	skin
13	chr6:129078200-129078600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr6:129078200-129079400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr6:129078600-129079400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:129079000-129084600	Weak transcription	HMEC	breast
17	chr6:129079200-129079600	Enhancers	Fetal Heart	heart
18	chr6:129079400-129084600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr6:129079400-129084800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr6:129080600-129081000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:129081000-129081200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr6:129081000-129081200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr6:129081200-129083200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr6:129081200-129084400	Weak transcription	NHEK	skin
25	chr6:129081200-129084600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr6:129082000-129089000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:129083200-129083400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr6:129083200-129083400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr6:129083200-129083600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr6:129083600-129089000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr6:129083800-129084000	Enhancers	Right Ventricle	heart
32	chr6:129084400-129085400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr6:129084400-129085600	Enhancers	NHEK	skin
34	chr6:129084600-129085000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr6:129084600-129085600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr6:129084600-129085600	Enhancers	HMEC	breast
37	chr6:129084800-129085000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:129084800-129085200	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr6:129084800-129085400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:129087000-129087200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr6:129088600-129089600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:129089000-129089600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr6:129089000-129089600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:129089000-129090000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
45	chr6:129089200-129089600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr6:129102600-129103400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr6:129102600-129103400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr6:129102600-129106000	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr6:129102800-129104400	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr6:129103400-129104000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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