Variant report

Variant	nsv1021063
Chromosome Location	chr6:245786-303121
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1405)
CpG islands
(count:977)
Chromatin interactive
region (count:52)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:269760-269795	K562	blood:	n/a	n/a
2	ATF1	chr6:272562-272614	K562	blood:	n/a	n/a
3	ATF1	chr6:246458-246690	K562	blood:	n/a	n/a
4	ATF2	chr6:286192-288235	GM12878	blood:	n/a	n/a
5	ATF2	chr6:286268-287911	GM12878	blood:	n/a	n/a
6	ATF2	chr6:251841-252484	GM12878	blood:	n/a	n/a
7	ATF2	chr6:252707-253298	GM12878	blood:	n/a	n/a
8	ATF2	chr6:292427-294467	GM12878	blood:	n/a	n/a
9	ATF2	chr6:271011-271641	GM12878	blood:	n/a	n/a
10	ATF2	chr6:295807-297437	GM12878	blood:	n/a	n/a
11	ATF2	chr6:259642-260384	GM12878	blood:	n/a	n/a
12	ATF2	chr6:298148-299448	GM12878	blood:	n/a	n/a
13	ATF2	chr6:290281-294331	GM12878	blood:	n/a	n/a
14	ATF2	chr6:295599-298070	GM12878	blood:	n/a	n/a
15	ATF2	chr6:270995-271517	GM12878	blood:	n/a	n/a
16	ATF2	chr6:290519-292253	GM12878	blood:	n/a	n/a
17	ATF2	chr6:259708-260417	GM12878	blood:	n/a	n/a
18	ATF2	chr6:250519-251229	GM12878	blood:	n/a	n/a
19	ATF2	chr6:250576-251222	GM12878	blood:	n/a	n/a
20	BACH1	chr6:291630-292342	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr6:286581-287101	GM12878	blood:	n/a	n/a
22	BATF	chr6:296144-296807	GM12878	blood:	n/a	n/a
23	BATF	chr6:255760-256053	GM12878	blood:	n/a	n/a
24	BATF	chr6:291187-292336	GM12878	blood:	n/a	chr6:291698-291708
25	BATF	chr6:253185-253459	GM12878	blood:	n/a	chr6:253319-253330
26	BATF	chr6:250687-251007	GM12878	blood:	n/a	n/a
27	BATF	chr6:298533-299065	GM12878	blood:	n/a	n/a
28	BATF	chr6:292716-293771	GM12878	blood:	n/a	n/a
29	BATF	chr6:251975-252282	GM12878	blood:	n/a	chr6:252121-252132
30	BATF	chr6:270933-271475	GM12878	blood:	n/a	n/a
31	BATF	chr6:251891-252302	GM12878	blood:	n/a	chr6:252121-252132
32	BATF	chr6:270957-271443	GM12878	blood:	n/a	n/a
33	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
34	BCL11A	chr6:291491-292047	GM12878	blood:	n/a	chr6:291951-291964 chr6:291664-291677 chr6:292017-292030
35	BCL11A	chr6:292445-293648	GM12878	blood:	n/a	chr6:292688-292697 chr6:292592-292601 chr6:292449-292462 chr6:292676-292685
36	BCL11A	chr6:292491-293124	GM12878	blood:	n/a	chr6:292688-292697 chr6:292592-292601 chr6:292676-292685
37	BCL3	chr6:251918-252257	GM12878	blood:	n/a	n/a
38	BCL3	chr6:250633-251099	GM12878	blood:	n/a	n/a
39	BCL3	chr6:291125-292019	GM12878	blood:	n/a	chr6:291951-291964 chr6:291664-291677
40	BCL3	chr6:286364-287200	GM12878	blood:	n/a	chr6:286463-286471 chr6:286725-286734
41	BCL3	chr6:296110-296940	GM12878	blood:	n/a	n/a
42	BCL3	chr6:253073-253545	GM12878	blood:	n/a	chr6:253319-253328 chr6:253318-253327
43	BCL3	chr6:291068-293696	GM12878	blood:	n/a	chr6:291951-291964 chr6:291664-291677 chr6:292688-292697 chr6:292592-292601 chr6:292121-292134 chr6:292449-292462 chr6:292242-292255 chr6:292304-292317 chr6:292017-292030 chr6:292080-292093 chr6:292676-292685
44	BCLAF1	chr6:294538-295523	GM12878	blood:	n/a	n/a
45	BCLAF1	chr6:295809-297115	GM12878	blood:	n/a	n/a
46	BCLAF1	chr6:290341-294155	GM12878	blood:	n/a	chr6:291951-291964 chr6:291664-291677 chr6:292688-292697 chr6:292592-292601 chr6:292121-292134 chr6:292449-292462 chr6:292242-292255 chr6:292304-292317 chr6:292017-292030 chr6:292080-292093 chr6:292676-292685
47	BCLAF1	chr6:271149-271667	GM12878	blood:	n/a	n/a
48	BCLAF1	chr6:286486-288018	GM12878	blood:	n/a	chr6:286725-286734
49	BCLAF1	chr6:251864-252358	GM12878	blood:	n/a	n/a
50	BCLAF1	chr6:290043-295209	GM12878	blood:	n/a	chr6:291951-291964 chr6:291664-291677 chr6:292688-292697 chr6:292592-292601 chr6:292121-292134 chr6:292449-292462 chr6:292242-292255 chr6:292304-292317 chr6:292017-292030 chr6:292080-292093 chr6:292676-292685

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:293285-293335	AG09309	skin:	n/a
2	chr6:293285-293335	AG09309	skin:	n/a
3	chr6:292823-292873	HCPEpiC	choroid plexus:	n/a
4	chr6:291687-291737	HRPEpiC	eye:	n/a
5	chr6:290800-290850	HMEC	breast:	n/a
6	chr6:297974-298024	NH-A	brain:	n/a
7	chr6:292522-292572	PrEC	prostate:	n/a
8	chr6:292329-292379	K562	blood:	n/a
9	chr6:292385-292435	GM12892	blood:	n/a
10	chr6:299762-299812	HPAEpiC	pulmonary alveolar:	n/a
11	chr6:299762-299812	SK-N-MC	brain:	n/a
12	chr6:291903-291953	BE2_C	brain:	n/a
13	chr6:292823-292873	NHDF-neo	bronchial:	n/a
14	chr6:291903-291953	BJ	skin:	n/a
15	chr6:297974-298024	HMEC	breast:	n/a
16	chr6:291882-291932	HRE	kidney:	n/a
17	chr6:291909-291959	HepG2	liver:	n/a
18	chr6:291687-291737	HCT-116	colon:	n/a
19	chr6:292823-292873	K562	blood:	n/a
20	chr6:293285-293335	HepG2	liver:	n/a
21	chr6:293285-293335	NHBE	bronchial:	n/a
22	chr6:291687-291737	GM12891	blood:	n/a
23	chr6:292522-292572	HCM	heart:	n/a
24	chr6:292522-292572	Hela-S3	cervix:	n/a
25	chr6:292596-292646	SAEC	small airway:	n/a
26	chr6:290800-290850	NHDF-neo	bronchial:	n/a
27	chr6:292596-292646	SK-N-MC	brain:	n/a
28	chr6:291909-291959	CMK	blood:	n/a
29	chr6:290800-290850	HPAEpiC	pulmonary alveolar:	n/a
30	chr6:296538-296588	Hepatocyte	liver:	n/a
31	chr6:291882-291932	NHDF-neo	bronchial:	n/a
32	chr6:296538-296588	PFSK-1	brain:	n/a
33	chr6:299762-299812	ovcar-3	ovarian:	n/a
34	chr6:291903-291953	Hela-S3	cervix:	n/a
35	chr6:292329-292379	NHBE	bronchial:	n/a
36	chr6:296538-296588	GM12892	blood:	n/a
37	chr6:293285-293335	ProgFib	skin:	n/a
38	chr6:296538-296588	NHBE	bronchial:	n/a
39	chr6:292329-292379	SK-N-SH_RA	brain:	n/a
40	chr6:290800-290850	HCM	heart:	n/a
41	chr6:292385-292435	HMEC	breast:	n/a
42	chr6:292385-292435	NB4	blood:	n/a
43	chr6:297974-298024	HCM	heart:	n/a
44	chr6:292329-292379	SK-N-MC	brain:	n/a
45	chr6:296538-296588	HRE	kidney:	n/a
46	chr6:292596-292646	A549	lung:	n/a
47	chr6:293331-293381	HRE	kidney:	n/a
48	chr6:299762-299812	AoSMC	blood vessel:	n/a
49	chr6:291882-291932	AG04449	skin:	fetal
50	chr6:293331-293381	ProgFib	skin:	n/a

(count:52 , 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	chr17:17719893..17722583-chr6:302740..304240,2	MCF-7	breast:
3	chr6:257661..259747-chr6:263345..265684,2	K562	blood:
4	chr6:272456..276094-chr6:277811..280765,3	K562	blood:
5	chr18:77866631..77867571-chr6:292442..293062,2	Hela-S3	cervix:
6	chr6:287235..289508-chr6:291225..294248,4	MCF-7	breast:
7	chr17:56736004..56736702-chr6:292106..292878,2	MCF-7	breast:
8	chr6:295536..297795-chr6:305679..308154,2	K562	blood:
9	chr6:296050..297928-chr6:302031..303581,2	K562	blood:
10	chr19:37018814..37019652-chr6:292056..292904,2	Hela-S3	cervix:
11	chr6:285371..287917-chr6:411939..414727,2	MCF-7	breast:
12	chr6:295238..298761-chr6:302352..305820,5	MCF-7	breast:
13	chr12:6579777..6580703-chr6:291768..292740,2	Hela-S3	cervix:
14	chr6:294663..298192-chr6:299302..301728,3	MCF-7	breast:
15	chr19:30206179..30206679-chr6:291771..292378,2	HCT-116	colon:
16	chr6:299057..300641-chr6:314619..316749,2	MCF-7	breast:
17	chr6:294663..298192-chr6:299302..301728,3	MCF-7	breast:
18	chr6:291553..295786-chr6:297288..306010,11	K562	blood:
19	chr6:296050..300472-chr6:301997..308154,8	K562	blood:
20	chr6:296231..298975-chr6:325413..327737,2	MCF-7	breast:
21	chr6:256291..258797-chr6:266153..268904,2	K562	blood:
22	chr6:256291..258797-chr6:266153..268904,2	K562	blood:
23	chr6:284765..286882-chr6:287879..289536,2	MCF-7	breast:
24	chr16:30076765..30077507-chr6:291393..292212,2	Hela-S3	cervix:
25	chr6:296173..299152-chr6:320389..322030,2	K562	blood:
26	chr6:302147..303918-chr6:305942..308442,2	MCF-7	breast:
27	chr6:257661..259747-chr6:263345..265684,2	K562	blood:
28	chr6:293351..295006-chr6:303551..305599,2	MCF-7	breast:
29	chr6:296050..300472-chr6:301997..308154,8	K562	blood:
30	chr6:257151..259180-chr6:290748..292745,2	MCF-7	breast:
31	chr6:256291..259560-chr6:266153..268904,3	K562	blood:
32	chr6:291597..293239-chr6:294137..296291,2	K562	blood:
33	chr6:281531..285813-chr6:290498..294393,5	MCF-7	breast:
34	chr6:296050..297928-chr6:302031..303581,2	K562	blood:
35	chr6:290910..293038-chr6:302160..304078,2	MCF-7	breast:
36	chr12:49658539..49660530-chr6:290672..293249,2	MCF-7	breast:
37	chr6:291185..292858-chr6:298724..301310,3	MCF-7	breast:
38	chr6:295238..298761-chr6:302352..305820,5	MCF-7	breast:
39	chr11:62608627..62609393-chr6:291557..292282,3	HCT-116	colon:
40	chr17:48943450..48944099-chr6:292243..292871,2	Hela-S3	cervix:
41	chr6:272456..276094-chr6:277811..280765,3	K562	blood:
42	chr6:292029..292761-chr9:35489964..35490895,2	Hela-S3	cervix:
43	chr6:273516..275258-chr6:282028..283733,2	K562	blood:
44	chr6:256291..259560-chr6:266153..268904,3	K562	blood:
45	chr20:37074974..37076110-chr6:292160..292999,3	Hela-S3	cervix:
46	chr6:273516..275258-chr6:282028..283733,2	K562	blood:
47	chr6:278056..279662-chr6:281316..283230,2	MCF-7	breast:
48	chr6:302781..304461-chr6:306575..308896,2	MCF-7	breast:
49	chr6:278056..279662-chr6:281316..283230,2	MCF-7	breast:
50	chr6:284765..286882-chr6:287879..289536,2	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	chr6:285321-285384	XLOC_005567
3	lnc-EXOC2-3	chr6:277864-278155	XLOC_005567

No data

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

Extended variants
information (count: 2552 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2552 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569474807	chr6:245818-245819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs374625228	chr6:245859-245860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554875971	chr6:245892-245893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192165082	chr6:245925-245926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141096798	chr6:245975-245976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150279872	chr6:245992-245993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553907528	chr6:245993-245994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544702024	chr6:245997-245998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs367556238	chr6:246064-246065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572960170	chr6:246081-246082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184242698	chr6:246113-246114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111327074	chr6:246173-246174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs13213850	chr6:246178-246179	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs544446166	chr6:246179-246180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375247579	chr6:246203-246204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75098038	chr6:246226-246227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529938495	chr6:246229-246230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148934341	chr6:246281-246282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560237575	chr6:246373-246374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs367575553	chr6:246414-246415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532439420	chr6:246443-246444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145672818	chr6:246445-246446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569195290	chr6:246475-246476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531917508	chr6:246527-246528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138327177	chr6:246530-246531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371413966	chr6:246579-246580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs78442283	chr6:246621-246622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534431109	chr6:246628-246629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77688705	chr6:246629-246630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566595013	chr6:246663-246664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371879124	chr6:246672-246673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114923636	chr6:246680-246681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558269603	chr6:246696-246697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188677729	chr6:246767-246768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs71548192	chr6:246771-246772	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs554881472	chr6:246819-246820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146241301	chr6:246835-246836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181238509	chr6:246910-246911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559884197	chr6:246956-246957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11319547	chr6:246966-246967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532482035	chr6:246976-246977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs70982826	chr6:246982-246983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149000248	chr6:246983-246984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs77537345	chr6:246984-246985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544833050	chr6:247005-247006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555602405	chr6:247009-247010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572113830	chr6:247073-247074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375224813	chr6:247099-247100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545848486	chr6:247107-247108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535629828	chr6:247114-247115	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:1371 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:236800-255400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr6:247400-247600	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr6:247400-248400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr6:247400-248400	Enhancers	Primary B cells from peripheral blood	blood
5	chr6:247400-248400	Enhancers	GM12878-XiMat	blood
6	chr6:247400-248800	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr6:247600-249000	Enhancers	Primary B cells from cord blood	blood
8	chr6:247800-252200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr6:248400-249800	Weak transcription	Primary B cells from peripheral blood	blood
10	chr6:248400-250000	Weak transcription	GM12878-XiMat	blood
11	chr6:248400-250600	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr6:248800-250600	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr6:248800-252000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr6:249000-250000	Weak transcription	Primary B cells from cord blood	blood
15	chr6:249800-250000	Enhancers	Primary B cells from peripheral blood	blood
16	chr6:250000-250400	Weak transcription	Primary B cells from peripheral blood	blood
17	chr6:250000-251000	Enhancers	Primary B cells from cord blood	blood
18	chr6:250000-251800	Enhancers	GM12878-XiMat	blood
19	chr6:250400-251400	Enhancers	Primary B cells from peripheral blood	blood
20	chr6:250600-251200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr6:250600-251200	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr6:250600-251400	Enhancers	Primary T cells from cord blood	blood
23	chr6:250600-252800	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr6:250600-252800	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr6:250600-258400	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr6:250800-251000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr6:250800-251200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr6:250800-251200	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr6:250800-253400	Enhancers	NHEK	skin
30	chr6:251000-251800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr6:251000-251800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
32	chr6:251000-254800	Weak transcription	Primary B cells from cord blood	blood
33	chr6:251200-251400	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr6:251200-255400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr6:251200-257200	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr6:251200-259400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr6:251400-252000	Weak transcription	Primary T cells from cord blood	blood
38	chr6:251400-252600	Weak transcription	Primary B cells from peripheral blood	blood
39	chr6:251400-255400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr6:251600-253400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr6:251800-252000	Enhancers	Hela-S3	cervix
42	chr6:251800-252200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:251800-252800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr6:251800-253000	Enhancers	HMEC	breast
45	chr6:251800-253400	Flanking Active TSS	GM12878-XiMat	blood
46	chr6:251800-253600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
47	chr6:251800-254000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr6:252000-252600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr6:252000-253400	Enhancers	Primary T cells from cord blood	blood
50	chr6:252000-253400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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