Variant report

Variant	nsv970682
Chromosome Location	chr6:54325591-54375255
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	BACH1	chr6:54356311-54356514	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr6:54357824-54358432	HCT-116	colon:	n/a	n/a
3	CEBPB	chr6:54359429-54359584	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr6:54357925-54358248	IMR90	lung:	n/a	n/a
5	CEBPB	chr6:54357794-54358385	HCT-116	colon:	n/a	n/a
6	CHD2	chr6:54328670-54328680	GM12878	blood:	n/a	n/a
7	CTCF	chr6:54345783-54345788	GM19238	blood:	n/a	n/a
8	CTCF	chr6:54327854-54327891	GM10248	blood:	n/a	n/a
9	CTCF	chr6:54345161-54345253	GM13976	blood:	n/a	n/a
10	CTCF	chr6:54345760-54345910	GM06990	blood:	n/a	n/a
11	CTCF	chr6:54345794-54345823	GM19238	blood:	n/a	n/a
12	E2F4	chr6:54358013-54358370	MCF10A-Er-Src	breast:	n/a	n/a
13	EBF1	chr6:54334765-54334828	GM12878	blood:	n/a	n/a
14	EP300	chr6:54357935-54358258	Hela-S3	cervix:	n/a	chr6:54358130-54358139
15	FOS	chr6:54356273-54356673	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr6:54357949-54358318	MCF10A-Er-Src	breast:	n/a	chr6:54358129-54358139 chr6:54358130-54358138 chr6:54358129-54358139 chr6:54358130-54358137 chr6:54358131-54358142 chr6:54358128-54358139 chr6:54358130-54358138 chr6:54358129-54358139
17	FOS	chr6:54356283-54356630	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr6:54356262-54356674	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr6:54356299-54356629	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr6:54357898-54358326	MCF10A-Er-Src	breast:	n/a	chr6:54358129-54358139 chr6:54358130-54358138 chr6:54358129-54358139 chr6:54358130-54358137 chr6:54358131-54358142 chr6:54358128-54358139 chr6:54358130-54358138 chr6:54358129-54358139
21	FOS	chr6:54357937-54358363	HUVEC	blood vessel:	n/a	chr6:54358129-54358139 chr6:54358130-54358138 chr6:54358129-54358139 chr6:54358130-54358137 chr6:54358131-54358142 chr6:54358128-54358139 chr6:54358130-54358138 chr6:54358129-54358139
22	FOS	chr6:54357950-54358282	MCF10A-Er-Src	breast:	n/a	chr6:54358129-54358139 chr6:54358130-54358138 chr6:54358129-54358139 chr6:54358130-54358137 chr6:54358131-54358142 chr6:54358128-54358139 chr6:54358130-54358138 chr6:54358129-54358139
23	FOS	chr6:54357967-54358316	MCF10A-Er-Src	breast:	n/a	chr6:54358129-54358139 chr6:54358130-54358138 chr6:54358129-54358139 chr6:54358130-54358137 chr6:54358131-54358142 chr6:54358128-54358139 chr6:54358130-54358138 chr6:54358129-54358139
24	FOSL1	chr6:54357898-54358429	HCT-116	colon:	n/a	chr6:54358129-54358139 chr6:54358130-54358138 chr6:54358129-54358139 chr6:54358130-54358137 chr6:54358131-54358142 chr6:54358130-54358138 chr6:54358129-54358139
25	FOSL1	chr6:54357878-54358408	HCT-116	colon:	n/a	chr6:54358129-54358139 chr6:54358130-54358138 chr6:54358129-54358139 chr6:54358130-54358137 chr6:54358131-54358142 chr6:54358130-54358138 chr6:54358129-54358139
26	FOSL2	chr6:54357835-54358380	SK-N-SH	brain:	n/a	chr6:54358129-54358139 chr6:54358130-54358138 chr6:54358129-54358139 chr6:54358130-54358137 chr6:54358131-54358142 chr6:54358130-54358138 chr6:54358129-54358139
27	FOSL2	chr6:54357975-54358326	SK-N-SH	brain:	n/a	chr6:54358129-54358139 chr6:54358130-54358138 chr6:54358129-54358139 chr6:54358130-54358137 chr6:54358131-54358142 chr6:54358130-54358138 chr6:54358129-54358139
28	FOSL2	chr6:54357975-54358323	A549	lung:	n/a	chr6:54358129-54358139 chr6:54358130-54358138 chr6:54358129-54358139 chr6:54358130-54358137 chr6:54358131-54358142 chr6:54358130-54358138 chr6:54358129-54358139
29	FOSL2	chr6:54358020-54358184	A549	lung:	n/a	chr6:54358129-54358139 chr6:54358130-54358138 chr6:54358129-54358139 chr6:54358130-54358137 chr6:54358131-54358142 chr6:54358130-54358138 chr6:54358129-54358139
30	FOXP2	chr6:54339742-54340020	SK-N-MC	brain:	n/a	n/a
31	GATA3	chr6:54335327-54335530	SH-SY5Y	brain:	n/a	n/a
32	GTF2F1	chr6:54325809-54325819	K562	blood:	n/a	n/a
33	HNF4A	chr6:54345904-54346170	HepG2	liver:	n/a	n/a
34	HNF4A	chr6:54345969-54346165	HepG2	liver:	n/a	n/a
35	JUN	chr6:54368161-54368210	HepG2	liver:	n/a	chr6:54368169-54368182
36	JUND	chr6:54328267-54328669	H1-hESC	embryonic stem cell:	n/a	n/a
37	JUND	chr6:54357790-54358389	HCT-116	colon:	n/a	chr6:54358129-54358139 chr6:54358130-54358138 chr6:54358129-54358139 chr6:54358130-54358137 chr6:54358131-54358142 chr6:54358130-54358138 chr6:54358129-54358139
38	JUND	chr6:54338206-54338477	HCT-116	colon:	n/a	n/a
39	JUND	chr6:54367777-54368304	HepG2	liver:	n/a	n/a
40	MAFF	chr6:54339820-54340147	HepG2	liver:	n/a	chr6:54339994-54340012
41	MAFK	chr6:54372596-54372812	HepG2	liver:	n/a	n/a
42	MAFK	chr6:54357992-54358316	IMR90	lung:	n/a	n/a
43	MAFK	chr6:54339814-54340151	HepG2	liver:	n/a	n/a
44	MAFK	chr6:54339804-54340165	HepG2	liver:	n/a	n/a
45	MAFK	chr6:54339900-54340114	IMR90	lung:	n/a	n/a
46	MAFK	chr6:54348193-54348232	HepG2	liver:	n/a	chr6:54348205-54348221
47	MAX	chr6:54357123-54357125	A549	lung:	n/a	n/a
48	MXI1	chr6:54327875-54327878	GM12878	blood:	n/a	n/a
49	MYC	chr6:54339517-54339563	H1-hESC	embryonic stem cell:	n/a	n/a
50	MYC	chr6:54356338-54356573	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:54328858-54328908	SKMC	muscle:	n/a
2	chr6:54328858-54328908	AG09319	gingival:	n/a
3	chr6:54328858-54328908	PANC-1	pancreas:	n/a
4	chr6:54328858-54328908	MCF10A-Er-Src	breast:	n/a
5	chr6:54328858-54328908	NHBE	bronchial:	n/a
6	chr6:54328858-54328908	SAEC	small airway:	n/a
7	chr6:54328858-54328908	HCM	heart:	n/a
8	chr6:54328858-54328908	MCF-7	breast:	n/a
9	chr6:54328858-54328908	HRCEpiC	kidney:	n/a
10	chr6:54328858-54328908	SK-N-SH_RA	brain:	n/a
11	chr6:54328858-54328908	AG04449	skin:	fetal
12	chr6:54328858-54328908	T-47D	breast:	n/a
13	chr6:54328858-54328908	IMR90	lung:	fetal
14	chr6:54328858-54328908	PFSK-1	brain:	n/a
15	chr6:54328858-54328908	BJ	skin:	n/a
16	chr6:54328858-54328908	Hela-S3	cervix:	n/a
17	chr6:54328858-54328908	K562	blood:	n/a
18	chr6:54328858-54328908	NHDF-neo	bronchial:	n/a
19	chr6:54328858-54328908	GM12878	blood:	n/a
20	chr6:54328858-54328908	Hepatocyte	liver:	n/a
21	chr6:54328858-54328908	PrEC	prostate:	n/a
22	chr6:54328858-54328908	ovcar-3	ovarian:	n/a
23	chr6:54328858-54328908	HAEpiC	amniotic membrane:	n/a
24	chr6:54328858-54328908	AG04450	lung:	fetal
25	chr6:54328858-54328908	HPAEpiC	pulmonary alveolar:	n/a
26	chr6:54328858-54328908	LNCaP	prostate:	n/a
27	chr6:54328858-54328908	AG09309	skin:	n/a
28	chr6:54328858-54328908	SK-N-SH	brain:	n/a
29	chr6:54328858-54328908	HEEpiC	esophagus:	n/a
30	chr6:54328858-54328908	GM12891	blood:	n/a
31	chr6:54328858-54328908	CMK	blood:	n/a
32	chr6:54328858-54328908	U87	brain:	n/a
33	chr6:54328858-54328908	GM06990	blood:	n/a
34	chr6:54328858-54328908	ECC-1	luminal epithelium:	n/a
35	chr6:54328858-54328908	AoSMC	blood vessel:	n/a
36	chr6:54328858-54328908	ProgFib	skin:	n/a
37	chr6:54328858-54328908	Jurkat	blood:	n/a
38	chr6:54328858-54328908	RPTEC	kidney:	n/a
39	chr6:54328858-54328908	HCT-116	colon:	n/a
40	chr6:54328858-54328908	NH-A	brain:	n/a
41	chr6:54328858-54328908	HIPEpiC	eye:	n/a
42	chr6:54328858-54328908	SK-N-MC	brain:	n/a
43	chr6:54328858-54328908	HCF	heart:	n/a
44	chr6:54328858-54328908	HNPCEpiC	eye:	n/a
45	chr6:54328858-54328908	GM19239	blood:	n/a
46	chr6:54328858-54328908	HRE	kidney:	n/a
47	chr6:54328858-54328908	NB4	blood:	n/a
48	chr6:54328858-54328908	GM12892	blood:	n/a
49	chr6:54328858-54328908	HL-60	blood:	n/a
50	chr6:54328858-54328908	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:54337437..54340096-chr6:54340126..54342389,2	MCF-7	breast:
2	chr6:54334351..54336130-chr6:54337919..54340373,2	MCF-7	breast:
3	chr6:54337437..54340096-chr6:54340126..54342389,2	MCF-7	breast:
4	chr6:54334351..54336130-chr6:54337919..54340373,2	MCF-7	breast:

Variant related genes	Relation type
CLNS1AP1	TF binding region
CLNS1AP1	CpG island

Extended variants
information (count: 1605 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1605 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549027685	chr6:54327800-54327801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565665147	chr6:54327828-54327829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528411950	chr6:54327839-54327840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186133406	chr6:54327845-54327846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113296392	chr6:54327850-54327851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146916433	chr6:54327855-54327856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536804473	chr6:54327861-54327862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144552867	chr6:54327917-54327918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557109147	chr6:54327918-54327919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs372147873	chr6:54327920-54327921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs151323207	chr6:54327944-54327945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535531880	chr6:54327959-54327960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190988153	chr6:54327965-54327966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182059317	chr6:54327979-54327980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187912740	chr6:54327994-54327995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541331191	chr6:54327999-54328000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192671737	chr6:54328071-54328072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs578191941	chr6:54328112-54328113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs6927952	chr6:54328115-54328116	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs563636920	chr6:54328149-54328150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529015011	chr6:54328164-54328165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542710776	chr6:54328214-54328215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559413792	chr6:54328221-54328222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528042930	chr6:54328278-54328279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115874632	chr6:54328288-54328289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565071740	chr6:54328300-54328301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530826961	chr6:54328309-54328310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550530699	chr6:54328355-54328356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs243773	chr6:54328358-54328359	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs183444152	chr6:54328364-54328365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369745264	chr6:54328488-54328489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549036283	chr6:54328490-54328491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565747315	chr6:54328524-54328525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs112802821	chr6:54328525-54328526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558130773	chr6:54328541-54328542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs578207978	chr6:54328554-54328555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140567124	chr6:54328570-54328571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557290300	chr6:54328575-54328576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574258830	chr6:54328599-54328600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113394515	chr6:54328600-54328601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188279613	chr6:54328601-54328602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543598992	chr6:54328625-54328626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544723253	chr6:54328643-54328644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563587478	chr6:54328698-54328699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs76399549	chr6:54328777-54328778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530747860	chr6:54328784-54328785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550817408	chr6:54328808-54328809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560946183	chr6:54328848-54328849	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529800170	chr6:54328851-54328852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546381934	chr6:54328859-54328860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	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
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54327800-54329000	Enhancers	HSMMtube	muscle
2	chr6:54328200-54328800	Enhancers	H9 Cell Line	embryonic stem cell
3	chr6:54328200-54328800	Enhancers	NHEK	skin
4	chr6:54328200-54329000	Enhancers	HSMM	muscle
5	chr6:54328400-54328800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr6:54328400-54328800	Enhancers	H1 Cell Line	embryonic stem cell
7	chr6:54328400-54328800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr6:54328400-54328800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr6:54328400-54328800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr6:54328400-54328800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr6:54328400-54328800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:54328400-54329000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr6:54328400-54329000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr6:54328800-54338200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr6:54329000-54338200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:54336400-54336600	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr6:54336400-54336600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr6:54336600-54338400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr6:54336600-54338600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr6:54337000-54339800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr6:54338200-54338600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr6:54338200-54338800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:54338200-54338800	Enhancers	NHEK	skin
24	chr6:54338200-54339000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr6:54338400-54338800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr6:54338600-54339200	Enhancers	H1 Cell Line	embryonic stem cell
27	chr6:54338600-54339200	Enhancers	H9 Cell Line	embryonic stem cell
28	chr6:54338600-54339200	Enhancers	Placenta Amnion	Placenta Amnion
29	chr6:54338600-54339400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr6:54346000-54346400	Enhancers	Gastric	stomach
31	chr6:54352800-54355400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr6:54355200-54358400	Enhancers	HMEC	breast
33	chr6:54355400-54356000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr6:54355400-54358000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr6:54355400-54358400	Enhancers	NHEK	skin
36	chr6:54355600-54358800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr6:54355800-54356400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr6:54355800-54356400	Enhancers	Placenta Amnion	Placenta Amnion
39	chr6:54355800-54357600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:54356000-54356400	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr6:54356000-54357800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr6:54356400-54356800	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr6:54356800-54358400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr6:54357000-54358400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr6:54357600-54358200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr6:54357600-54358200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr6:54357600-54358400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr6:54357800-54358200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr6:54357800-54358200	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr6:54357800-54358200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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