Variant report

Variant	nsv600746
Chromosome Location	chr6:237215-311938
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1803)
CpG islands
(count:978)
Chromatin interactive
region (count:68)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1803 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:311696-312014	K562	blood:	n/a	n/a
2	ATF1	chr6:269760-269795	K562	blood:	n/a	n/a
3	ATF1	chr6:246458-246690	K562	blood:	n/a	n/a
4	ATF1	chr6:272562-272614	K562	blood:	n/a	n/a
5	ATF2	chr6:298148-299448	GM12878	blood:	n/a	n/a
6	ATF2	chr6:250519-251229	GM12878	blood:	n/a	n/a
7	ATF2	chr6:304636-306753	GM12878	blood:	n/a	n/a
8	ATF2	chr6:271011-271641	GM12878	blood:	n/a	n/a
9	ATF2	chr6:295807-297437	GM12878	blood:	n/a	n/a
10	ATF2	chr6:292427-294467	GM12878	blood:	n/a	n/a
11	ATF2	chr6:286192-288235	GM12878	blood:	n/a	n/a
12	ATF2	chr6:308768-309915	GM12878	blood:	n/a	n/a
13	ATF2	chr6:305067-306671	GM12878	blood:	n/a	n/a
14	ATF2	chr6:290281-294331	GM12878	blood:	n/a	n/a
15	ATF2	chr6:286268-287911	GM12878	blood:	n/a	n/a
16	ATF2	chr6:290519-292253	GM12878	blood:	n/a	n/a
17	ATF2	chr6:295599-298070	GM12878	blood:	n/a	n/a
18	ATF2	chr6:259642-260384	GM12878	blood:	n/a	n/a
19	ATF2	chr6:250576-251222	GM12878	blood:	n/a	n/a
20	ATF2	chr6:251841-252484	GM12878	blood:	n/a	n/a
21	ATF2	chr6:252707-253298	GM12878	blood:	n/a	n/a
22	ATF2	chr6:270995-271517	GM12878	blood:	n/a	n/a
23	ATF2	chr6:259708-260417	GM12878	blood:	n/a	n/a
24	BACH1	chr6:291630-292342	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr6:270933-271475	GM12878	blood:	n/a	n/a
26	BATF	chr6:270957-271443	GM12878	blood:	n/a	n/a
27	BATF	chr6:253185-253459	GM12878	blood:	n/a	chr6:253319-253330
28	BATF	chr6:305306-306216	GM12878	blood:	n/a	n/a
29	BATF	chr6:292716-293771	GM12878	blood:	n/a	n/a
30	BATF	chr6:251975-252282	GM12878	blood:	n/a	chr6:252121-252132
31	BATF	chr6:251891-252302	GM12878	blood:	n/a	chr6:252121-252132
32	BATF	chr6:286581-287101	GM12878	blood:	n/a	n/a
33	BATF	chr6:305823-306278	GM12878	blood:	n/a	n/a
34	BATF	chr6:255760-256053	GM12878	blood:	n/a	n/a
35	BATF	chr6:296144-296807	GM12878	blood:	n/a	n/a
36	BATF	chr6:250687-251007	GM12878	blood:	n/a	n/a
37	BATF	chr6:298533-299065	GM12878	blood:	n/a	n/a
38	BATF	chr6:291187-292336	GM12878	blood:	n/a	chr6:291698-291708
39	BCL11A	chr6:292445-293648	GM12878	blood:	n/a	chr6:292688-292697 chr6:292592-292601 chr6:292449-292462 chr6:292676-292685
40	BCL11A	chr6:308907-309223	GM12878	blood:	n/a	n/a
41	BCL11A	chr6:291086-292412	GM12878	blood:	n/a	chr6:291951-291964 chr6:291664-291677 chr6:292121-292134 chr6:292242-292255 chr6:292304-292317 chr6:292017-292030 chr6:292080-292093
42	BCL11A	chr6:292491-293124	GM12878	blood:	n/a	chr6:292688-292697 chr6:292592-292601 chr6:292676-292685
43	BCL11A	chr6:305397-306207	GM12878	blood:	n/a	n/a
44	BCL11A	chr6:291491-292047	GM12878	blood:	n/a	chr6:291951-291964 chr6:291664-291677 chr6:292017-292030
45	BCL11A	chr6:305163-306311	GM12878	blood:	n/a	n/a
46	BCL3	chr6:250633-251099	GM12878	blood:	n/a	n/a
47	BCL3	chr6:286364-287200	GM12878	blood:	n/a	chr6:286463-286471 chr6:286725-286734
48	BCL3	chr6:253073-253545	GM12878	blood:	n/a	chr6:253319-253328 chr6:253318-253327
49	BCL3	chr6:251918-252257	GM12878	blood:	n/a	n/a
50	BCL3	chr6:303172-303661	GM12878	blood:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:296538-296588	SKMC	muscle:	n/a
2	chr6:297974-298024	HepG2	liver:	n/a
3	chr6:296538-296588	SKMC	muscle:	n/a
4	chr6:297974-298024	HepG2	liver:	n/a
5	chr6:291903-291953	HCF	heart:	n/a
6	chr6:292385-292435	HCT-116	colon:	n/a
7	chr6:288505-288555	T-47D	breast:	n/a
8	chr6:292823-292873	HCF	heart:	n/a
9	chr6:290800-290850	HRE	kidney:	n/a
10	chr6:292329-292379	SK-N-MC	brain:	n/a
11	chr6:292823-292873	IMR90	lung:	fetal
12	chr6:291882-291932	HAEpiC	amniotic membrane:	n/a
13	chr6:293331-293381	BE2_C	brain:	n/a
14	chr6:293285-293335	Jurkat	blood:	n/a
15	chr6:299762-299812	NT2-D1	testis:	n/a
16	chr6:292329-292379	AoSMC	blood vessel:	n/a
17	chr6:291687-291737	Caco-2	colon:	n/a
18	chr6:291882-291932	AG04450	lung:	fetal
19	chr6:293285-293335	ProgFib	skin:	n/a
20	chr6:291903-291953	AG04450	lung:	fetal
21	chr6:292823-292873	GM19239	blood:	n/a
22	chr6:292329-292379	Caco-2	colon:	n/a
23	chr6:293331-293381	HRPEpiC	eye:	n/a
24	chr6:297974-298024	SKMC	muscle:	n/a
25	chr6:292329-292379	AG09309	skin:	n/a
26	chr6:296538-296588	NH-A	brain:	n/a
27	chr6:290800-290850	T-47D	breast:	n/a
28	chr6:291882-291932	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:296538-296588	NT2-D1	testis:	n/a
30	chr6:292522-292572	AoSMC	blood vessel:	n/a
31	chr6:293285-293335	HEK293	kidney:	embryo
32	chr6:292329-292379	HRPEpiC	eye:	n/a
33	chr6:297974-298024	HEK293	kidney:	embryo
34	chr6:288505-288555	HAEpiC	amniotic membrane:	n/a
35	chr6:291882-291932	CMK	blood:	n/a
36	chr6:292385-292435	H1-hESC	embryonic stem cell:	embryo
37	chr6:292823-292873	HNPCEpiC	eye:	n/a
38	chr6:293331-293381	IMR90	lung:	fetal
39	chr6:292823-292873	HCM	heart:	n/a
40	chr6:299762-299812	HRE	kidney:	n/a
41	chr6:292329-292379	NH-A	brain:	n/a
42	chr6:292596-292646	PFSK-1	brain:	n/a
43	chr6:297974-298024	AoSMC	blood vessel:	n/a
44	chr6:292522-292572	GM12891	blood:	n/a
45	chr6:296538-296588	Hela-S3	cervix:	n/a
46	chr6:291687-291737	HCM	heart:	n/a
47	chr6:291687-291737	HL-60	blood:	n/a
48	chr6:297974-298024	PANC-1	pancreas:	n/a
49	chr6:291903-291953	HNPCEpiC	eye:	n/a
50	chr6:291909-291959	HUVEC	blood vessel:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:292752..294756-chr6:308707..310835,2	MCF-7	breast:
2	chr6:284765..286882-chr6:287879..289536,2	MCF-7	breast:
3	chr6:291185..292858-chr6:298724..301310,3	MCF-7	breast:
4	chr6:273516..275258-chr6:282028..283733,2	K562	blood:
5	chr6:294663..298192-chr6:299302..301728,3	MCF-7	breast:
6	chr6:296050..297928-chr6:302031..303581,2	K562	blood:
7	chr6:295536..297795-chr6:305679..308154,2	K562	blood:
8	chr6:305778..307935-chr6:308138..311376,3	MCF-7	breast:
9	chr6:302147..303918-chr6:305942..308442,2	MCF-7	breast:
10	chr6:257661..259747-chr6:263345..265684,2	K562	blood:
11	chr6:256291..258797-chr6:266153..268904,2	K562	blood:
12	chr19:30206179..30206679-chr6:291771..292378,2	HCT-116	colon:
13	chr12:49658539..49660530-chr6:290672..293249,2	MCF-7	breast:
14	chr6:287235..289508-chr6:291225..294248,4	MCF-7	breast:
15	chr6:292752..294756-chr6:308707..310835,2	MCF-7	breast:
16	chr6:295238..298761-chr6:302352..305820,5	MCF-7	breast:
17	chr17:56736004..56736702-chr6:292106..292878,2	MCF-7	breast:
18	chr6:264177..266345-chr6:291888..293660,2	MCF-7	breast:
19	chr6:302147..303918-chr6:305942..308442,2	MCF-7	breast:
20	chr6:278056..279662-chr6:281316..283230,2	MCF-7	breast:
21	chr6:295238..298761-chr6:302352..305820,5	MCF-7	breast:
22	chr6:302781..304461-chr6:306575..308896,2	MCF-7	breast:
23	chr6:293351..295006-chr6:303551..305599,2	MCF-7	breast:
24	chr6:272456..276094-chr6:277811..280765,3	K562	blood:
25	chr6:296050..297928-chr6:302031..303581,2	K562	blood:
26	chr6:302781..304461-chr6:306575..308896,2	MCF-7	breast:
27	chr19:37018814..37019652-chr6:292056..292904,2	Hela-S3	cervix:
28	chr6:256291..258797-chr6:266153..268904,2	K562	blood:
29	chr6:281531..285813-chr6:290498..294393,5	MCF-7	breast:
30	chr20:37074974..37076110-chr6:292160..292999,3	Hela-S3	cervix:
31	chr6:296173..299152-chr6:320389..322030,2	K562	blood:
32	chr17:17719893..17722583-chr6:302740..304240,2	MCF-7	breast:
33	chr6:256291..259560-chr6:266153..268904,3	K562	blood:
34	chr6:303726..306245-chr6:306797..309200,2	K562	blood:
35	chr6:257661..259747-chr6:263345..265684,2	K562	blood:
36	chr6:278056..279662-chr6:281316..283230,2	MCF-7	breast:
37	chr6:299057..300641-chr6:314619..316749,2	MCF-7	breast:
38	chr6:256291..259560-chr6:266153..268904,3	K562	blood:
39	chr6:296050..300472-chr6:301997..308154,8	K562	blood:
40	chr6:294663..298192-chr6:299302..301728,3	MCF-7	breast:
41	chr6:272456..276094-chr6:277811..280765,3	K562	blood:
42	chr6:293351..295006-chr6:303551..305599,2	MCF-7	breast:
43	chr6:290870..294057-chr6:304196..308763,6	MCF-7	breast:
44	chr6:284765..286882-chr6:287879..289536,2	MCF-7	breast:
45	chr6:291775..293838-chr6:305753..308321,2	MCF-7	breast:
46	chr11:62608627..62609393-chr6:291557..292282,3	HCT-116	colon:
47	chr6:303609..305966-chr6:315490..317440,2	MCF-7	breast:
48	chr6:305647..307462-chr6:316653..319307,2	K562	blood:
49	chr6:291553..295786-chr6:297288..306010,11	K562	blood:
50	chr6:307230..309658-chr6:318745..320870,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXOC2-3	chr6:285915-286279	XLOC_005567
2	lnc-EXOC2-3	chr6:277864-278155	XLOC_005567
3	lnc-EXOC2-3	chr6:285321-285384	XLOC_005567

No data

Variant related genes	Relation type
DUSP22	TF binding region
DUSP22	CpG island
ENSG00000141232	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000254004	chromatin interactions
ENSG00000072310	chromatin interactions
ENSG00000167553	chromatin interactions
ENSG00000131943	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000101544	chromatin interactions
ENSG00000149925	chromatin interactions
ENSG00000228629	chromatin interactions
ENSG00000112679	chromatin interactions
ENSG00000229980	chromatin interactions
ENSG00000198853	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000139190	chromatin interactions
ENSG00000174365	chromatin interactions

Extended variants
information (count: 3402 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3402 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4959611	chr6:237215-237216	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183230415	chr6:237222-237223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539879784	chr6:237324-237325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4959612	chr6:237332-237333	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs188590012	chr6:237336-237337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567899965	chr6:237396-237397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540620566	chr6:237466-237467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148448265	chr6:237479-237480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34645088	chr6:237534-237535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs397887706	chr6:237545-237546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573405135	chr6:237550-237551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546044609	chr6:237551-237552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142625033	chr6:237558-237559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113543741	chr6:237559-237560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112171816	chr6:237562-237563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143524775	chr6:237566-237567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146660289	chr6:237567-237568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs140248752	chr6:237582-237583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570791556	chr6:237583-237584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs9501777	chr6:237584-237585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs193164614	chr6:237585-237586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570362309	chr6:237588-237589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536098784	chr6:237589-237590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555979661	chr6:237590-237591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574474010	chr6:237591-237592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577922837	chr6:237596-237597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374671236	chr6:237604-237605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7739881	chr6:237609-237610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149180082	chr6:237613-237614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375523763	chr6:237620-237621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562488680	chr6:237621-237622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575921003	chr6:237630-237631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143341777	chr6:237631-237632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368337749	chr6:237642-237643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542290727	chr6:237652-237653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112418211	chr6:237653-237654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547829839	chr6:237665-237666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564328986	chr6:237675-237676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs386695903	chr6:237676-237677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375119240	chr6:237677-237678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185057052	chr6:237686-237687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs13219192	chr6:237691-237692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551076250	chr6:237694-237695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529588893	chr6:237717-237718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549617303	chr6:237721-237722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566227754	chr6:237723-237724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112233322	chr6:237757-237758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533659277	chr6:237763-237764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553782607	chr6:237780-237781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369560024	chr6:237812-237813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1742 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:233400-240200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:236600-240200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr6:236800-240000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr6:236800-240200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr6:236800-240200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr6:236800-240200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr6:236800-241000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:236800-255400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr6:237000-238000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:237000-238000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr6:237000-241400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr6:237200-240400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:237200-241600	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr6:238000-238200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:238200-238400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr6:240000-240800	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr6:240200-240400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:240200-240600	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr6:240200-240600	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr6:240200-240800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr6:240200-241400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr6:240200-241800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr6:240400-240600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr6:240600-241000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:241000-241400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr6:241000-241600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:241200-241400	Bivalent Enhancer	Placenta	Placenta
28	chr6:241400-241600	Enhancers	H9 Cell Line	embryonic stem cell
29	chr6:241400-241800	Enhancers	Placenta	Placenta
30	chr6:241600-241800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr6:247400-247600	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr6:247400-248400	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr6:247400-248400	Enhancers	Primary B cells from peripheral blood	blood
34	chr6:247400-248400	Enhancers	GM12878-XiMat	blood
35	chr6:247400-248800	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr6:247600-249000	Enhancers	Primary B cells from cord blood	blood
37	chr6:247800-252200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr6:248400-249800	Weak transcription	Primary B cells from peripheral blood	blood
39	chr6:248400-250000	Weak transcription	GM12878-XiMat	blood
40	chr6:248400-250600	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr6:248800-250600	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr6:248800-252000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr6:249000-250000	Weak transcription	Primary B cells from cord blood	blood
44	chr6:249800-250000	Enhancers	Primary B cells from peripheral blood	blood
45	chr6:250000-250400	Weak transcription	Primary B cells from peripheral blood	blood
46	chr6:250000-251000	Enhancers	Primary B cells from cord blood	blood
47	chr6:250000-251800	Enhancers	GM12878-XiMat	blood
48	chr6:250400-251400	Enhancers	Primary B cells from peripheral blood	blood
49	chr6:250600-251200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr6:250600-251200	Enhancers	Primary T helper naive cells from peripheral blood	blood

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