Variant report

Variant	nsv600739
Chromosome Location	chr6:175522-253861
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2572)
CpG islands
(count:1159)
Chromatin interactive
region (count:55)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2572 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:221474-221994	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:220004-220874	HepG2	liver:	n/a	n/a
3	ATF1	chr6:232965-233203	K562	blood:	n/a	n/a
4	ATF1	chr6:246458-246690	K562	blood:	n/a	n/a
5	ATF2	chr6:231396-232311	GM12878	blood:	n/a	n/a
6	ATF2	chr6:193250-194551	GM12878	blood:	n/a	n/a
7	ATF2	chr6:188600-190870	GM12878	blood:	n/a	n/a
8	ATF2	chr6:230249-231059	GM12878	blood:	n/a	n/a
9	ATF2	chr6:235845-236520	GM12878	blood:	n/a	n/a
10	ATF2	chr6:193111-194543	GM12878	blood:	n/a	n/a
11	ATF2	chr6:181000-181701	GM12878	blood:	n/a	n/a
12	ATF2	chr6:217880-219360	GM12878	blood:	n/a	n/a
13	ATF2	chr6:217828-219955	GM12878	blood:	n/a	n/a
14	ATF2	chr6:235849-236489	GM12878	blood:	n/a	n/a
15	ATF2	chr6:216810-217515	GM12878	blood:	n/a	n/a
16	ATF2	chr6:216952-217397	GM12878	blood:	n/a	n/a
17	ATF2	chr6:250519-251229	GM12878	blood:	n/a	n/a
18	ATF2	chr6:188713-190294	GM12878	blood:	n/a	n/a
19	ATF2	chr6:251841-252484	GM12878	blood:	n/a	n/a
20	ATF2	chr6:224893-225951	GM12878	blood:	n/a	n/a
21	ATF2	chr6:228803-229965	GM12878	blood:	n/a	n/a
22	ATF2	chr6:217063-217455	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr6:209691-210220	GM12878	blood:	n/a	n/a
24	ATF2	chr6:230263-230821	GM12878	blood:	n/a	n/a
25	ATF2	chr6:252707-253298	GM12878	blood:	n/a	n/a
26	ATF2	chr6:224802-226028	GM12878	blood:	n/a	n/a
27	ATF2	chr6:250576-251222	GM12878	blood:	n/a	n/a
28	ATF2	chr6:226477-229964	GM12878	blood:	n/a	n/a
29	ATF2	chr6:220648-222383	GM12878	blood:	n/a	n/a
30	ATF2	chr6:226748-228552	GM12878	blood:	n/a	n/a
31	ATF2	chr6:231354-232300	GM12878	blood:	n/a	n/a
32	ATF2	chr6:209433-210258	GM12878	blood:	n/a	n/a
33	ATF2	chr6:181047-181898	GM12878	blood:	n/a	n/a
34	ATF2	chr6:221081-222611	GM12878	blood:	n/a	n/a
35	ATF3	chr6:219928-220235	K562	blood:	n/a	n/a
36	BACH1	chr6:220702-221015	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr6:209349-209668	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr6:219912-220319	H1-hESC	embryonic stem cell:	n/a	chr6:220124-220138
39	BACH1	chr6:219988-220177	K562	blood:	n/a	chr6:220124-220138
40	BATF	chr6:221656-222204	GM12878	blood:	n/a	chr6:221879-221890
41	BATF	chr6:218090-218656	GM12878	blood:	n/a	n/a
42	BATF	chr6:209735-210135	GM12878	blood:	n/a	n/a
43	BATF	chr6:181320-181669	GM12878	blood:	n/a	n/a
44	BATF	chr6:181382-181622	GM12878	blood:	n/a	n/a
45	BATF	chr6:251891-252302	GM12878	blood:	n/a	chr6:252121-252132
46	BATF	chr6:250687-251007	GM12878	blood:	n/a	n/a
47	BATF	chr6:231671-232067	GM12878	blood:	n/a	n/a
48	BATF	chr6:218763-219282	GM12878	blood:	n/a	n/a
49	BATF	chr6:193685-194335	GM12878	blood:	n/a	n/a
50	BATF	chr6:235921-236302	GM12878	blood:	n/a	n/a

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:202452-202502	MCF-7	breast:	n/a
2	chr6:235035-235085	HCF	heart:	n/a
3	chr6:209809-209859	GM12878	blood:	n/a
4	chr6:186671-186721	PrEC	prostate:	n/a
5	chr6:235035-235085	ovcar-3	ovarian:	n/a
6	chr6:224339-224389	SAEC	small airway:	n/a
7	chr6:236559-236609	AG09319	gingival:	n/a
8	chr6:202452-202502	HEK293	kidney:	embryo
9	chr6:230932-230982	U87	brain:	n/a
10	chr6:230959-231009	U87	brain:	n/a
11	chr6:226092-226142	HRE	kidney:	n/a
12	chr6:230908-230958	H1-hESC	embryonic stem cell:	embryo
13	chr6:235035-235085	PFSK-1	brain:	n/a
14	chr6:186671-186721	T-47D	breast:	n/a
15	chr6:179456-179506	HL-60	blood:	n/a
16	chr6:235035-235085	HUVEC	blood vessel:	n/a
17	chr6:209712-209762	HRE	kidney:	n/a
18	chr6:230959-231009	HRPEpiC	eye:	n/a
19	chr6:226092-226142	Hepatocyte	liver:	n/a
20	chr6:236559-236609	Hepatocyte	liver:	n/a
21	chr6:230908-230958	GM12878	blood:	n/a
22	chr6:235035-235085	T-47D	breast:	n/a
23	chr6:230908-230958	HCT-116	colon:	n/a
24	chr6:209763-209813	U87	brain:	n/a
25	chr6:225666-225716	AG04450	lung:	fetal
26	chr6:235035-235085	NB4	blood:	n/a
27	chr6:224713-224763	CMK	blood:	n/a
28	chr6:224713-224763	NH-A	brain:	n/a
29	chr6:230932-230982	RPTEC	kidney:	n/a
30	chr6:224713-224763	LNCaP	prostate:	n/a
31	chr6:202452-202502	GM12878	blood:	n/a
32	chr6:225666-225716	HNPCEpiC	eye:	n/a
33	chr6:209712-209762	SK-N-MC	brain:	n/a
34	chr6:235035-235085	HIPEpiC	eye:	n/a
35	chr6:179456-179506	HRCEpiC	kidney:	n/a
36	chr6:230932-230982	BJ	skin:	n/a
37	chr6:186671-186721	H1-hESC	embryonic stem cell:	embryo
38	chr6:202452-202502	NT2-D1	testis:	n/a
39	chr6:209712-209762	AG09309	skin:	n/a
40	chr6:209809-209859	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:202452-202502	ovcar-3	ovarian:	n/a
42	chr6:209809-209859	GM06990	blood:	n/a
43	chr6:235035-235085	NHBE	bronchial:	n/a
44	chr6:235035-235085	SKMC	muscle:	n/a
45	chr6:235035-235085	GM06990	blood:	n/a
46	chr6:225824-225874	T-47D	breast:	n/a
47	chr6:230908-230958	GM12891	blood:	n/a
48	chr6:224733-224783	A549	lung:	n/a
49	chr6:236559-236609	HCPEpiC	choroid plexus:	n/a
50	chr6:224733-224783	PFSK-1	brain:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:216802..217456-chr6:1436640..1437220,2	K562	blood:
2	chr6:182386..184733-chr6:187298..189526,2	K562	blood:
3	chr6:193592..196624-chr6:199092..202281,3	K562	blood:
4	chr6:188545..189282-chr6:373635..374544,3	MCF-7	breast:
5	chr6:181476..184276-chr6:186622..188907,2	MCF-7	breast:
6	chr6:188512..189290-chr6:408309..409342,5	K562	blood:
7	chr6:184999..187022-chr6:291843..294537,2	MCF-7	breast:
8	chr6:178419..181938-chr6:182767..184759,3	K562	blood:
9	chr6:228323..230023-chr6:368553..371061,2	K562	blood:
10	chr6:218667..220722-chr6:290754..293697,2	MCF-7	breast:
11	chr6:226271..228027-chr6:231480..233250,2	K562	blood:
12	chr6:226916..227829-chr6:408545..409059,2	K562	blood:
13	chr6:188540..189516-chr6:407870..409552,18	MCF-7	breast:
14	chr6:188865..189410-chr6:351061..352002,2	MCF-7	breast:
15	chr6:188184..189040-chr6:551172..552162,2	MCF-7	breast:
16	chr6:181320..184707-chr6:184919..187235,3	K562	blood:
17	chr6:204380..207081-chr6:218001..219962,2	K562	blood:
18	chr6:182386..184733-chr6:187298..189526,2	K562	blood:
19	chr6:188538..189926-chr6:408487..409481,6	MCF-7	breast:
20	chr6:221469..223469-chr6:224100..226474,2	K562	blood:
21	chr6:217204..217743-chr6:408573..409085,2	K562	blood:
22	chr6:190038..192340-chr6:196174..199027,2	K562	blood:
23	chr6:181320..184707-chr6:184919..187235,3	K562	blood:
24	chr6:187321..190676-chr6:193869..196032,3	K562	blood:
25	chr6:190038..192340-chr6:196174..199027,2	K562	blood:
26	chr6:196917..201263-chr6:202620..206119,4	K562	blood:
27	chr6:188398..189398-chr6:1436667..1437648,2	MCF-7	breast:
28	chr6:215085..218653-chr6:219608..222374,3	K562	blood:
29	chr6:221469..223469-chr6:224100..226474,2	K562	blood:
30	chr6:221194..223469-chr6:223525..225600,3	K562	blood:
31	chr6:188501..189288-chr6:558016..558846,2	MCF-7	breast:
32	chr6:221194..223469-chr6:223525..225600,3	K562	blood:
33	chr6:188817..189398-chr6:524504..525502,3	MCF-7	breast:
34	chr6:188750..189642-chr6:786566..787558,2	MCF-7	breast:
35	chr6:188851..189352-chr6:372580..373236,2	MCF-7	breast:
36	chr6:174671..177385-chr6:182024..184445,2	K562	blood:
37	chr6:181476..184276-chr6:186622..188907,2	MCF-7	breast:
38	chr6:174671..177385-chr6:182024..184445,2	K562	blood:
39	chr6:181397..184733-chr6:185247..188798,3	K562	blood:
40	chr6:215085..218653-chr6:219608..222374,3	K562	blood:
41	chr6:215135..217089-chr6:292102..293904,2	MCF-7	breast:
42	chr6:188655..189690-chr6:579041..579935,3	MCF-7	breast:
43	chr6:230872..233357-chr6:348225..349996,2	K562	blood:
44	chr6:181397..184733-chr6:185247..188798,3	K562	blood:
45	chr6:201924..204091-chr6:207759..211489,3	K562	blood:
46	chr6:187321..190676-chr6:193869..196032,3	K562	blood:
47	chr6:193592..196624-chr6:199092..202281,3	K562	blood:
48	chr6:190862..192633-chr6:194886..196390,2	MCF-7	breast:
49	chr6:189816..192061-chr6:402339..404478,2	K562	blood:
50	chr6:226271..228027-chr6:231480..233250,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL035696.1-2	chr6:183914-184371	XLOC_005117
2	lnc-EXOC2-6	chr6:198165-198509	ENSG00000263667.1
3	lnc-EXOC2-6	chr6:184593-184809	ENSG00000263667.1
4	lnc-EXOC2-6	chr6:186356-186561	ENSG00000263667.1
5	lnc-AL035696.1-1	chr6:205487-206392	ENSG00000205653.1
6	lnc-AL035696.1-2	chr6:184601-187741	XLOC_005117
7	lnc-EXOC2-17	chr6:222864-223155	l_3086_chr6:222863-230359_lymphNode
8	lnc-EXOC2-6	chr6:204887-205484	ENSG00000263667.1
9	lnc-EXOC2-6	chr6:187736-187906	ENSG00000263667.1
10	lnc-EXOC2-17	chr6:230321-230359	l_3086_chr6:222863-230359_lymphNode
11	lnc-EXOC2-6	chr6:189476-189649	ENSG00000263667.1
12	lnc-AL035696.1-2	chr6:186035-186494	NONHSAT105976
13	lnc-EXOC2-6	chr6:181466-181695	ENSG00000263667.1
14	lnc-AL035696.1-3	chr6:226079-226400	XLOC_005118
15	lnc-EXOC2-6	chr6:182366-182474	ENSG00000263667.1
16	lnc-AL035696.1-3	chr6:225686-226068	XLOC_005118
17	lnc-AL035696.1-2	chr6:184161-184371	NONHSAT105976
18	lnc-AL035696.1-1	chr6:203313-204413	ENSG00000205653.1
19	lnc-EXOC2-18	chr6:196682-196974	NONHSAT105977
20	lnc-AL035696.1-3	chr6:224950-225088	XLOC_005118

No data

Variant related genes	Relation type
ENSG00000218577	TF binding region
ENSG00000263667	TF binding region
ENSG00000205653	TF binding region
ENSG00000218577	CpG island
ENSG00000263667	CpG island
ENSG00000205653	CpG island
ENSG00000205653	chromatin interactions
ENSG00000263667	chromatin interactions
ENSG00000112679	chromatin interactions
TSC1	miRNA target sites
TRRAP	miRNA target sites

Extended variants
information (count: 3079 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:3079 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6596796	chr6:175522-175523	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554075153	chr6:175569-175570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs375316898	chr6:175606-175607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs6596797	chr6:175711-175712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6596798	chr6:175717-175718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369346084	chr6:175786-175787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369653996	chr6:175808-175809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115415279	chr6:175835-175836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200285339	chr6:175848-175849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144295141	chr6:175849-175850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148710256	chr6:175854-175855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577227008	chr6:175870-175871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373857523	chr6:175955-175956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372010342	chr6:176129-176130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115123990	chr6:176189-176190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369959126	chr6:176232-176233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372473983	chr6:176261-176262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545932461	chr6:176315-176316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556134239	chr6:176328-176329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112383627	chr6:176427-176428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543521725	chr6:176545-176546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs67751345	chr6:176721-176722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200800309	chr6:176742-176743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115768015	chr6:177015-177016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576063208	chr6:177024-177025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs17132995	chr6:177050-177051	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs377726171	chr6:177073-177074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371116733	chr6:177140-177141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112769533	chr6:177175-177176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs74834180	chr6:177219-177220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376777408	chr6:177328-177329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs386695890	chr6:177336-177337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543203905	chr6:177379-177380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375858751	chr6:177428-177429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146713805	chr6:177447-177448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189696699	chr6:177531-177532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541836841	chr6:177691-177692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201750725	chr6:177697-177698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371357188	chr6:177724-177725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4959127	chr6:177748-177749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114015413	chr6:177807-177808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573506603	chr6:177853-177854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142064167	chr6:177899-177900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374560782	chr6:177934-177935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528458022	chr6:177942-177943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545096645	chr6:177945-177946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs56407285	chr6:177952-177953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141246467	chr6:177961-177962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368708520	chr6:177979-177980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565555162	chr6:178110-178111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	20967226	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Breast cancer	21858162	CNVD

Chromatin state (count:1111 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:174800-178200	Weak transcription	Right Atrium	heart
2	chr6:177200-179600	Weak transcription	Primary B cells from peripheral blood	blood
3	chr6:178200-178400	ZNF genes & repeats	Right Atrium	heart
4	chr6:178200-178400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
5	chr6:178200-178600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
6	chr6:178200-179000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:178200-180200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:178400-192200	Weak transcription	Right Atrium	heart
9	chr6:179600-191800	Enhancers	Primary B cells from peripheral blood	blood
10	chr6:179800-180400	Enhancers	GM12878-XiMat	blood
11	chr6:180200-186600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr6:180200-190800	Enhancers	Primary B cells from cord blood	blood
13	chr6:180400-180600	Active TSS	Primary T cells from cord blood	blood
14	chr6:180400-180800	Enhancers	Fetal Thymus	thymus
15	chr6:180400-181200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
16	chr6:180400-181200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr6:180400-181400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr6:180400-181800	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr6:180400-181800	Active TSS	Thymus	Thymus
20	chr6:180400-182000	Flanking Active TSS	GM12878-XiMat	blood
21	chr6:180600-180800	Enhancers	Primary hematopoietic stem cells	blood
22	chr6:180600-181000	Flanking Active TSS	Primary T cells from cord blood	blood
23	chr6:180600-181000	Enhancers	Spleen	Spleen
24	chr6:180600-181200	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr6:180600-181400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr6:180600-181400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr6:180800-181000	Flanking Active TSS	Fetal Thymus	thymus
28	chr6:180800-181200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
29	chr6:180800-186800	Weak transcription	Primary hematopoietic stem cells	blood
30	chr6:181000-181400	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr6:181000-181400	Enhancers	Fetal Thymus	thymus
32	chr6:181000-181800	Enhancers	Primary T cells from cord blood	blood
33	chr6:181000-194800	Weak transcription	Spleen	Spleen
34	chr6:181200-183600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr6:181200-194400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr6:181400-183200	Weak transcription	Fetal Thymus	thymus
37	chr6:181400-188800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr6:181800-183600	Weak transcription	Thymus	Thymus
39	chr6:181800-184200	Weak transcription	Primary T cells from cord blood	blood
40	chr6:181800-188800	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr6:182000-184800	Enhancers	GM12878-XiMat	blood
42	chr6:183200-187800	Enhancers	Fetal Thymus	thymus
43	chr6:183600-184800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr6:183600-188000	Enhancers	Thymus	Thymus
45	chr6:184200-184600	Enhancers	Primary T cells from cord blood	blood
46	chr6:184200-184800	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr6:184200-184800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr6:184600-188800	Weak transcription	Primary T cells from cord blood	blood
49	chr6:184800-186400	Weak transcription	GM12878-XiMat	blood
50	chr6:184800-188800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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