Variant report

Variant	nsv1032802
Chromosome Location	chr6:149649-196357
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1352)
CpG islands
(count:183)
Chromatin interactive
region (count:39)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1352 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:168940-169157	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:157406-157408	K562	blood:	n/a	n/a
3	ATF2	chr6:188713-190294	GM12878	blood:	n/a	n/a
4	ATF2	chr6:193250-194551	GM12878	blood:	n/a	n/a
5	ATF2	chr6:154306-155179	GM12878	blood:	n/a	n/a
6	ATF2	chr6:181000-181701	GM12878	blood:	n/a	n/a
7	ATF2	chr6:188600-190870	GM12878	blood:	n/a	n/a
8	ATF2	chr6:156670-157032	GM12878	blood:	n/a	n/a
9	ATF2	chr6:150091-150623	GM12878	blood:	n/a	n/a
10	ATF2	chr6:193111-194543	GM12878	blood:	n/a	n/a
11	ATF2	chr6:154275-155106	GM12878	blood:	n/a	n/a
12	ATF2	chr6:181047-181898	GM12878	blood:	n/a	n/a
13	ATF2	chr6:152980-153487	GM12878	blood:	n/a	n/a
14	BATF	chr6:181320-181669	GM12878	blood:	n/a	n/a
15	BATF	chr6:154252-155133	GM12878	blood:	n/a	n/a
16	BATF	chr6:189313-189787	GM12878	blood:	n/a	n/a
17	BATF	chr6:183781-184092	GM12878	blood:	n/a	n/a
18	BATF	chr6:153034-153312	GM12878	blood:	n/a	n/a
19	BATF	chr6:150238-150522	GM12878	blood:	n/a	n/a
20	BATF	chr6:188701-189864	GM12878	blood:	n/a	chr6:189809-189818
21	BATF	chr6:156491-157009	GM12878	blood:	n/a	n/a
22	BATF	chr6:193685-194335	GM12878	blood:	n/a	n/a
23	BATF	chr6:154691-155030	GM12878	blood:	n/a	n/a
24	BATF	chr6:152968-153416	GM12878	blood:	n/a	chr6:153318-153326
25	BATF	chr6:181382-181622	GM12878	blood:	n/a	n/a
26	BATF	chr6:154197-154629	GM12878	blood:	n/a	n/a
27	BATF	chr6:156683-156991	GM12878	blood:	n/a	n/a
28	BCL11A	chr6:156633-157058	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:153082-153258	GM12878	blood:	n/a	n/a
30	BCL11A	chr6:154309-155065	GM12878	blood:	n/a	n/a
31	BCL11A	chr6:181394-181586	GM12878	blood:	n/a	chr6:181481-181490
32	BCL11A	chr6:193667-194343	GM12878	blood:	n/a	n/a
33	BCL11A	chr6:156702-156991	GM12878	blood:	n/a	n/a
34	BCL11A	chr6:152949-153344	GM12878	blood:	n/a	n/a
35	BCL11A	chr6:189288-190044	GM12878	blood:	n/a	n/a
36	BCL11A	chr6:189370-189693	GM12878	blood:	n/a	n/a
37	BCL3	chr6:193087-193559	GM12878	blood:	n/a	n/a
38	BCL3	chr6:189188-189736	GM12878	blood:	n/a	n/a
39	BCL3	chr6:154271-155009	GM12878	blood:	n/a	n/a
40	BCL3	chr6:155810-156195	GM12878	blood:	n/a	n/a
41	BCL3	chr6:188736-190047	GM12878	blood:	n/a	n/a
42	BCL3	chr6:194683-195018	GM12878	blood:	n/a	n/a
43	BCL3	chr6:181242-181640	GM12878	blood:	n/a	chr6:181481-181490
44	BCL3	chr6:154627-155012	GM12878	blood:	n/a	n/a
45	BCL3	chr6:193067-194409	GM12878	blood:	n/a	n/a
46	BCL3	chr6:193640-194390	GM12878	blood:	n/a	n/a
47	BCLAF1	chr6:193289-194435	GM12878	blood:	n/a	n/a
48	BCLAF1	chr6:188679-190442	GM12878	blood:	n/a	n/a
49	BCLAF1	chr6:181165-181751	GM12878	blood:	n/a	chr6:181481-181490
50	BCLAF1	chr6:193619-194351	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:186671-186721	IMR90	lung:	fetal
2	chr6:186671-186721	NHDF-neo	bronchial:	n/a
3	chr6:179659-179709	T-47D	breast:	n/a
4	chr6:179456-179506	Hepatocyte	liver:	n/a
5	chr6:186671-186721	NHBE	bronchial:	n/a
6	chr6:179456-179506	SKMC	muscle:	n/a
7	chr6:186671-186721	HPAEpiC	pulmonary alveolar:	n/a
8	chr6:186671-186721	AG10803	skin:	n/a
9	chr6:179659-179709	HCM	heart:	n/a
10	chr6:179659-179709	HEEpiC	esophagus:	n/a
11	chr6:179659-179709	GM12878	blood:	n/a
12	chr6:186671-186721	AG09309	skin:	n/a
13	chr6:179456-179506	NT2-D1	testis:	n/a
14	chr6:179456-179506	HCPEpiC	choroid plexus:	n/a
15	chr6:179659-179709	ProgFib	skin:	n/a
16	chr6:179456-179506	AG04450	lung:	fetal
17	chr6:179456-179506	HIPEpiC	eye:	n/a
18	chr6:186671-186721	HNPCEpiC	eye:	n/a
19	chr6:179456-179506	HepG2	liver:	n/a
20	chr6:179456-179506	AoSMC	blood vessel:	n/a
21	chr6:186671-186721	NH-A	brain:	n/a
22	chr6:186671-186721	HepG2	liver:	n/a
23	chr6:179456-179506	Jurkat	blood:	n/a
24	chr6:186671-186721	PANC-1	pancreas:	n/a
25	chr6:186671-186721	MCF10A-Er-Src	breast:	n/a
26	chr6:179659-179709	ECC-1	luminal epithelium:	n/a
27	chr6:179456-179506	GM06990	blood:	n/a
28	chr6:186671-186721	Hela-S3	cervix:	n/a
29	chr6:179659-179709	GM06990	blood:	n/a
30	chr6:179659-179709	HNPCEpiC	eye:	n/a
31	chr6:179659-179709	NHDF-neo	bronchial:	n/a
32	chr6:186671-186721	NT2-D1	testis:	n/a
33	chr6:179456-179506	SAEC	small airway:	n/a
34	chr6:179456-179506	CMK	blood:	n/a
35	chr6:179456-179506	H1-hESC	embryonic stem cell:	embryo
36	chr6:186671-186721	HCM	heart:	n/a
37	chr6:179456-179506	HNPCEpiC	eye:	n/a
38	chr6:179659-179709	HCF	heart:	n/a
39	chr6:186671-186721	HCT-116	colon:	n/a
40	chr6:179456-179506	HRPEpiC	eye:	n/a
41	chr6:186671-186721	ProgFib	skin:	n/a
42	chr6:179659-179709	HEK293	kidney:	embryo
43	chr6:186671-186721	ECC-1	luminal epithelium:	n/a
44	chr6:179659-179709	IMR90	lung:	fetal
45	chr6:179659-179709	LNCaP	prostate:	n/a
46	chr6:179659-179709	Caco-2	colon:	n/a
47	chr6:179456-179506	RPTEC	kidney:	n/a
48	chr6:179456-179506	GM12891	blood:	n/a
49	chr6:186671-186721	GM12892	blood:	n/a
50	chr6:179659-179709	MCF10A-Er-Src	breast:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:188817..189398-chr6:524504..525502,3	MCF-7	breast:
2	chr6:174671..177385-chr6:182024..184445,2	K562	blood:
3	chr6:162155..164910-chr6:167837..169506,2	K562	blood:
4	chr6:181397..184733-chr6:185247..188798,3	K562	blood:
5	chr6:178419..181938-chr6:182767..184759,3	K562	blood:
6	chr6:162155..164910-chr6:167837..169506,2	K562	blood:
7	chr6:189816..192061-chr6:402339..404478,2	K562	blood:
8	chr6:190038..192340-chr6:196174..199027,2	K562	blood:
9	chr6:182386..184733-chr6:187298..189526,2	K562	blood:
10	chr6:174671..177385-chr6:182024..184445,2	K562	blood:
11	chr6:188184..189040-chr6:551172..552162,2	MCF-7	breast:
12	chr6:184999..187022-chr6:291843..294537,2	MCF-7	breast:
13	chr6:187321..190676-chr6:193869..196032,3	K562	blood:
14	chr6:188512..189290-chr6:408309..409342,5	K562	blood:
15	chr6:188538..189926-chr6:408487..409481,6	MCF-7	breast:
16	chr6:193592..196624-chr6:199092..202281,3	K562	blood:
17	chr6:190038..192340-chr6:196174..199027,2	K562	blood:
18	chr4:28899..29522-chr6:156896..157400,2	MCF-7	breast:
19	chr6:181397..184733-chr6:185247..188798,3	K562	blood:
20	chr6:181320..184707-chr6:184919..187235,3	K562	blood:
21	chr6:182386..184733-chr6:187298..189526,2	K562	blood:
22	chr6:190862..192633-chr6:194886..196390,2	MCF-7	breast:
23	chr6:178419..181938-chr6:182767..184759,3	K562	blood:
24	chr6:188545..189282-chr6:373635..374544,3	MCF-7	breast:
25	chr6:187321..190676-chr6:193869..196032,3	K562	blood:
26	chr6:181476..184276-chr6:186622..188907,2	MCF-7	breast:
27	chr6:188509..189446-chr6:686215..686918,2	MCF-7	breast:
28	chr4:29168..29759-chr6:156896..157405,3	MCF-7	breast:
29	chr6:188750..189642-chr6:786566..787558,2	MCF-7	breast:
30	chr6:190862..192633-chr6:194886..196390,2	MCF-7	breast:
31	chr6:188615..189306-chr6:374006..374509,2	MCF-7	breast:
32	chr6:188865..189410-chr6:351061..352002,2	MCF-7	breast:
33	chr6:188851..189352-chr6:372580..373236,2	MCF-7	breast:
34	chr6:188398..189398-chr6:1436667..1437648,2	MCF-7	breast:
35	chr6:188540..189516-chr6:407870..409552,18	MCF-7	breast:
36	chr6:188655..189690-chr6:579041..579935,3	MCF-7	breast:
37	chr6:181476..184276-chr6:186622..188907,2	MCF-7	breast:
38	chr6:181320..184707-chr6:184919..187235,3	K562	blood:
39	chr6:188501..189288-chr6:558016..558846,2	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXOC2-6	chr6:189476-189649	ENSG00000263667.1
2	lnc-AL035696.1-5	chr6:156546-156639	XLOC_005116
3	lnc-EXOC2-20	chr6:168171-170561	NONHSAT105972
4	lnc-EXOC2-6	chr6:186356-186561	ENSG00000263667.1
5	lnc-AL035696.1-5	chr6:155135-155395	XLOC_005116
6	lnc-EXOC2-6	chr6:182366-182474	ENSG00000263667.1
7	lnc-EXOC2-20	chr6:171827-172220	NONHSAT105972
8	lnc-AL035696.1-6	chr6:171079-171400	NONHSAT105973
9	lnc-AL035696.1-6	chr6:170686-171068	NONHSAT105973
10	lnc-AL035696.1-5	chr6:156119-156514	XLOC_005116
11	lnc-EXOC2-20	chr6:167607-167826	NONHSAT105971
12	lnc-AL035696.1-6	chr6:169950-170088	NONHSAT105973
13	lnc-AL035696.1-2	chr6:186035-186494	NONHSAT105976
14	lnc-EXOC2-20	chr6:169545-169753	NONHSAT105971
15	lnc-EXOC2-6	chr6:184593-184809	ENSG00000263667.1
16	lnc-AL035696.1-2	chr6:183914-184371	XLOC_005117
17	lnc-EXOC2-6	chr6:187736-187906	ENSG00000263667.1
18	lnc-AL035696.1-2	chr6:184601-187741	XLOC_005117
19	lnc-AL035696.1-2	chr6:184161-184371	NONHSAT105976
20	lnc-EXOC2-6	chr6:181466-181695	ENSG00000263667.1
21	lnc-EXOC2-20	chr6:170352-170631	NONHSAT105971

No data

Variant related genes	Relation type
ENSG00000218577	TF binding region
CICP18	TF binding region
LINC00266-3	TF binding region
ENSG00000218577	CpG island
CICP18	CpG island
LINC00266-3	CpG island
ENSG00000112679	chromatin interactions
TRRAP	miRNA target sites
TSC1	miRNA target sites

Extended variants
information (count: 769 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:769 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200473207	chr6:149664-149665	ZNF genes & repeats Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs113631972	chr6:149688-149689	ZNF genes & repeats Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs73719522	chr6:149691-149692	ZNF genes & repeats Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs371285253	chr6:149778-149779	ZNF genes & repeats Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs115760718	chr6:149861-149862	ZNF genes & repeats Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs563808184	chr6:149876-149877	ZNF genes & repeats Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs538060833	chr6:149883-149884	ZNF genes & repeats Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs555075250	chr6:149897-149898	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs199566231	chr6:149901-149902	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs200932599	chr6:149921-149922	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs201157505	chr6:150042-150043	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs372336391	chr6:150061-150062	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs199644782	chr6:150063-150064	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200476119	chr6:150075-150076	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201353567	chr6:150081-150082	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376357913	chr6:150128-150129	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112255647	chr6:150205-150206	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114742453	chr6:150272-150273	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372717328	chr6:150273-150274	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373819375	chr6:150276-150277	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34229051	chr6:150279-150280	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs367672030	chr6:150282-150283	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371276125	chr6:150301-150302	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374959203	chr6:150317-150318	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372494995	chr6:150327-150328	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200806289	chr6:150329-150330	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114111661	chr6:150371-150372	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115477643	chr6:150372-150373	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79355852	chr6:150395-150396	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75092964	chr6:150396-150397	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs80182130	chr6:150462-150463	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200991702	chr6:150473-150474	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs116785107	chr6:150535-150536	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116475101	chr6:150536-150537	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201082475	chr6:150567-150568	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs117246822	chr6:150574-150575	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530098440	chr6:150577-150578	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369147025	chr6:150580-150581	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113927280	chr6:150602-150603	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs151059005	chr6:150604-150605	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200224602	chr6:150629-150630	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2079315	chr6:150639-150640	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201252262	chr6:150660-150661	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146084888	chr6:150661-150662	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140854789	chr6:150677-150678	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144767274	chr6:150730-150731	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79005627	chr6:150744-150745	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs151012310	chr6:150761-150762	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373482633	chr6:150808-150809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543145295	chr6:150878-150879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Prader-willi syndrome	20588305	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
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
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	22495311	CNVD
small cell lung cancer	20016488	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:148800-150400	Weak transcription	Right Atrium	heart
2	chr6:149400-150800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr6:149400-151000	Enhancers	Thymus	Thymus
4	chr6:149400-154200	Enhancers	GM12878-XiMat	blood
5	chr6:149600-149800	Enhancers	Fetal Thymus	thymus
6	chr6:149800-153400	Weak transcription	Fetal Thymus	thymus
7	chr6:150200-150800	Enhancers	Primary T cells from cord blood	blood
8	chr6:150200-151000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr6:150400-150800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr6:151000-151400	Weak transcription	Thymus	Thymus
11	chr6:151400-152000	Enhancers	Thymus	Thymus
12	chr6:151800-152400	Enhancers	Placenta	Placenta
13	chr6:151800-155200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:151800-155600	Enhancers	HMEC	breast
15	chr6:152000-153200	Weak transcription	Thymus	Thymus
16	chr6:152400-154000	Weak transcription	Placenta	Placenta
17	chr6:152800-153600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr6:153000-153400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr6:153000-155000	Enhancers	NHEK	skin
20	chr6:153200-153800	Enhancers	Thymus	Thymus
21	chr6:153400-154000	Enhancers	Fetal Thymus	thymus
22	chr6:153400-154800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr6:153600-154600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr6:153800-154200	Weak transcription	Thymus	Thymus
25	chr6:153800-154200	Enhancers	NHDF-Ad	bronchial
26	chr6:153800-157400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr6:154000-155800	Weak transcription	Fetal Thymus	thymus
28	chr6:154000-157000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:154200-154400	Enhancers	Placenta	Placenta
30	chr6:154200-154400	Enhancers	Thymus	Thymus
31	chr6:154200-154400	Flanking Active TSS	GM12878-XiMat	blood
32	chr6:154200-154600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr6:154200-155000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr6:154200-156200	Weak transcription	NHDF-Ad	bronchial
35	chr6:154400-154600	Enhancers	GM12878-XiMat	blood
36	chr6:154400-156200	Weak transcription	Thymus	Thymus
37	chr6:154600-155000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr6:154600-155200	Flanking Active TSS	GM12878-XiMat	blood
39	chr6:154600-155200	Enhancers	Osteobl	bone
40	chr6:154600-156200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr6:155000-155200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr6:155000-155200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
43	chr6:155000-155200	Enhancers	NHLF	lung
44	chr6:155200-156200	Weak transcription	NHLF	lung
45	chr6:155200-156400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:155200-156600	Weak transcription	Osteobl	bone
47	chr6:155200-157000	Enhancers	GM12878-XiMat	blood
48	chr6:155600-156000	Weak transcription	HMEC	breast
49	chr6:155600-158000	Enhancers	Adipose Nuclei	Adipose
50	chr6:155800-158000	Enhancers	Fetal Thymus	thymus

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