Variant report

Variant	esv2763602
Chromosome Location	chr6:150581193-150720666
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2058)
CpG islands
(count:488)
Chromatin interactive
region (count:130)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2058 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:150654386-150654755	K562	blood:	n/a	n/a
2	ARID3A	chr6:150592169-150594225	K562	blood:	n/a	n/a
3	ARID3A	chr6:150641709-150642002	K562	blood:	n/a	n/a
4	ARID3A	chr6:150656204-150656655	K562	blood:	n/a	n/a
5	ARID3A	chr6:150614380-150615000	K562	blood:	n/a	n/a
6	ARID3A	chr6:150716580-150716874	K562	blood:	n/a	n/a
7	ARID3A	chr6:150588787-150589697	K562	blood:	n/a	n/a
8	ARID3A	chr6:150648358-150648558	K562	blood:	n/a	n/a
9	ARID3A	chr6:150644374-150644606	K562	blood:	n/a	n/a
10	ARID3A	chr6:150590022-150590355	K562	blood:	n/a	n/a
11	ARID3A	chr6:150716561-150716901	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:150597304-150598299	K562	blood:	n/a	n/a
13	ATF1	chr6:150592451-150593521	K562	blood:	n/a	n/a
14	ATF1	chr6:150593903-150594397	K562	blood:	n/a	n/a
15	ATF1	chr6:150638926-150639223	K562	blood:	n/a	n/a
16	ATF1	chr6:150690117-150690163	K562	blood:	n/a	n/a
17	ATF1	chr6:150597401-150597785	K562	blood:	n/a	n/a
18	ATF1	chr6:150618482-150618795	K562	blood:	n/a	n/a
19	ATF1	chr6:150588851-150589268	K562	blood:	n/a	n/a
20	ATF1	chr6:150623376-150623768	K562	blood:	n/a	n/a
21	ATF1	chr6:150614623-150615231	K562	blood:	n/a	n/a
22	ATF1	chr6:150633636-150633837	K562	blood:	n/a	n/a
23	ATF2	chr6:150657487-150657954	GM12878	blood:	n/a	n/a
24	ATF3	chr6:150614600-150614969	K562	blood:	n/a	n/a
25	ATF3	chr6:150614470-150615109	HCT-116	colon:	n/a	n/a
26	ATF3	chr6:150623415-150623648	K562	blood:	n/a	n/a
27	ATF3	chr6:150638827-150639224	K562	blood:	n/a	n/a
28	ATF3	chr6:150598882-150599149	K562	blood:	n/a	n/a
29	ATF3	chr6:150610700-150610879	K562	blood:	n/a	chr6:150610772-150610781
30	ATF3	chr6:150592970-150593702	K562	blood:	n/a	n/a
31	BACH1	chr6:150698678-150699081	K562	blood:	n/a	n/a
32	BACH1	chr6:150664992-150665189	K562	blood:	n/a	n/a
33	BACH1	chr6:150594126-150594326	K562	blood:	n/a	chr6:150594262-150594276
34	BACH1	chr6:150597658-150597664	K562	blood:	n/a	n/a
35	BATF	chr6:150595146-150595471	GM12878	blood:	n/a	n/a
36	BATF	chr6:150623375-150623659	GM12878	blood:	n/a	chr6:150623523-150623534 chr6:150623524-150623534 chr6:150623541-150623552
37	BATF	chr6:150657444-150657852	GM12878	blood:	n/a	n/a
38	BATF	chr6:150625697-150625938	GM12878	blood:	n/a	n/a
39	BATF	chr6:150657445-150657910	GM12878	blood:	n/a	n/a
40	BATF	chr6:150623336-150623737	GM12878	blood:	n/a	chr6:150623523-150623534 chr6:150623524-150623534 chr6:150623541-150623552
41	BCL11A	chr6:150657375-150657914	GM12878	blood:	n/a	n/a
42	BCL11A	chr6:150657438-150657964	GM12878	blood:	n/a	n/a
43	BCL11A	chr6:150585120-150585481	GM12878	blood:	n/a	n/a
44	BCL3	chr6:150585089-150585329	GM12878	blood:	n/a	n/a
45	BCL3	chr6:150653755-150654205	GM12878	blood:	n/a	n/a
46	BCL3	chr6:150654416-150654785	GM12878	blood:	n/a	n/a
47	BCL3	chr6:150654358-150654690	GM12878	blood:	n/a	n/a
48	BCL3	chr6:150653722-150654257	GM12878	blood:	n/a	n/a
49	BCL3	chr6:150691143-150691743	GM12878	blood:	n/a	n/a
50	BCL3	chr6:150585121-150585362	GM12878	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150589148-150589198	AG10803	skin:	n/a
2	chr6:150690143-150690193	U87	brain:	n/a
3	chr6:150690143-150690193	HCT-116	colon:	n/a
4	chr6:150689918-150689968	RPTEC	kidney:	n/a
5	chr6:150589148-150589198	HCM	heart:	n/a
6	chr6:150688748-150688798	GM06990	blood:	n/a
7	chr6:150585229-150585279	SKMC	muscle:	n/a
8	chr6:150688748-150688798	BE2_C	brain:	n/a
9	chr6:150688748-150688798	NT2-D1	testis:	n/a
10	chr6:150689918-150689968	SK-N-MC	brain:	n/a
11	chr6:150697210-150697260	GM12878	blood:	n/a
12	chr6:150589148-150589198	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:150688748-150688798	HL-60	blood:	n/a
14	chr6:150585229-150585279	Jurkat	blood:	n/a
15	chr6:150689918-150689968	Hela-S3	cervix:	n/a
16	chr6:150716612-150716662	ovcar-3	ovarian:	n/a
17	chr6:150689918-150689968	HL-60	blood:	n/a
18	chr6:150716612-150716662	AG10803	skin:	n/a
19	chr6:150690125-150690175	AG10803	skin:	n/a
20	chr6:150690143-150690193	GM06990	blood:	n/a
21	chr6:150690143-150690193	NB4	blood:	n/a
22	chr6:150690143-150690193	GM12892	blood:	n/a
23	chr6:150689918-150689968	ovcar-3	ovarian:	n/a
24	chr6:150716612-150716662	NHBE	bronchial:	n/a
25	chr6:150690125-150690175	Caco-2	colon:	n/a
26	chr6:150697210-150697260	SKMC	muscle:	n/a
27	chr6:150585229-150585279	PANC-1	pancreas:	n/a
28	chr6:150689918-150689968	U87	brain:	n/a
29	chr6:150697210-150697260	AoSMC	blood vessel:	n/a
30	chr6:150688748-150688798	GM12892	blood:	n/a
31	chr6:150690125-150690175	BJ	skin:	n/a
32	chr6:150688748-150688798	RPTEC	kidney:	n/a
33	chr6:150690125-150690175	HIPEpiC	eye:	n/a
34	chr6:150585229-150585279	GM12878	blood:	n/a
35	chr6:150690143-150690193	HL-60	blood:	n/a
36	chr6:150697210-150697260	MCF-7	breast:	n/a
37	chr6:150697210-150697260	SAEC	small airway:	n/a
38	chr6:150690143-150690193	SK-N-SH_RA	brain:	n/a
39	chr6:150688748-150688798	SAEC	small airway:	n/a
40	chr6:150690125-150690175	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:150690125-150690175	SKMC	muscle:	n/a
42	chr6:150690143-150690193	AG10803	skin:	n/a
43	chr6:150697210-150697260	T-47D	breast:	n/a
44	chr6:150589148-150589198	AoSMC	blood vessel:	n/a
45	chr6:150689918-150689968	SAEC	small airway:	n/a
46	chr6:150716612-150716662	MCF10A-Er-Src	breast:	n/a
47	chr6:150689918-150689968	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:150716612-150716662	U87	brain:	n/a
49	chr6:150585229-150585279	AG04450	lung:	fetal
50	chr6:150697210-150697260	HRPEpiC	eye:	n/a

(count:130 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:150642390..150644728-chr6:150645013..150646951,2	K562	blood:
2	chr6:150595217..150598289-chr6:150598347..150601921,4	K562	blood:
3	chr6:150566857..150569459-chr6:150586928..150589779,2	K562	blood:
4	chr6:150576665..150578563-chr6:150593687..150595296,2	MCF-7	breast:
5	chr6:150637450..150641855-chr6:150642003..150645154,6	K562	blood:
6	chr6:150602972..150605153-chr6:150605339..150607461,2	K562	blood:
7	chr6:150673808..150674705-chr6:150716343..150716873,3	MCF-7	breast:
8	chr6:150585889..150591234-chr6:150591941..150595727,5	MCF-7	breast:
9	chr6:150632599..150634459-chr6:150636479..150638879,2	K562	blood:
10	chr6:150620693..150625949-chr6:150627495..150632317,8	K562	blood:
11	chr6:150392325..150392932-chr6:150655903..150657072,4	K562	blood:
12	chr6:150644840..150646705-chr6:150652961..150654511,2	K562	blood:
13	chr6:150588773..150591393-chr6:150591530..150593093,2	MCF-7	breast:
14	chr6:150585671..150587274-chr6:150589357..150590923,2	MCF-7	breast:
15	chr6:150531888..150534706-chr6:150587953..150589817,2	K562	blood:
16	chr6:150668412..150670441-chr6:150671071..150673551,2	K562	blood:
17	chr6:150717285..150719589-chr6:150720584..150722449,2	K562	blood:
18	chr6:150664294..150666420-chr6:150694752..150697036,2	MCF-7	breast:
19	chr6:150401499..150402158-chr6:150713934..150714468,2	K562	blood:
20	chr6:150632599..150634459-chr6:150636479..150638879,2	K562	blood:
21	chr6:150609494..150611063-chr6:150611238..150612780,2	K562	blood:
22	chr6:150583389..150586556-chr6:150586926..150590915,4	MCF-7	breast:
23	chr6:150607126..150608753-chr6:150627355..150629999,2	K562	blood:
24	chr6:150487734..150491272-chr6:150592346..150595301,4	K562	blood:
25	chr6:150673211..150675475-chr6:150711661..150714265,2	MCF-7	breast:
26	chr6:150673415..150676875-chr6:150682312..150685340,3	K562	blood:
27	chr6:150717285..150719589-chr6:150720584..150722449,2	K562	blood:
28	chr6:150592207..150594581-chr6:150595847..150597727,2	K562	blood:
29	chr6:150588773..150591393-chr6:150591530..150593093,2	MCF-7	breast:
30	chr6:150598333..150600619-chr6:150603264..150605565,3	K562	blood:
31	chr6:150633237..150635111-chr6:150636965..150639804,2	MCF-7	breast:
32	chr6:150401711..150402469-chr6:150716292..150716821,2	K562	blood:
33	chr6:150667580..150669709-chr6:150673147..150675127,2	MCF-7	breast:
34	chr6:150673415..150676875-chr6:150682312..150685340,3	K562	blood:
35	chr6:150582199..150585734-chr6:150587276..150589096,3	K562	blood:
36	chr6:150465090..150467055-chr6:150662955..150664731,2	K562	blood:
37	chr6:150642390..150644728-chr6:150645013..150646951,2	K562	blood:
38	chr6:150607126..150608753-chr6:150627355..150629999,2	K562	blood:
39	chr6:150667580..150669709-chr6:150673147..150675127,2	MCF-7	breast:
40	chr6:150642041..150644950-chr6:150645013..150647968,3	K562	blood:
41	chr6:150701386..150704723-chr6:150704966..150707708,3	K562	blood:
42	chr6:150588320..150590630-chr6:150595998..150597655,2	K562	blood:
43	chr6:150585889..150591234-chr6:150591941..150595727,5	MCF-7	breast:
44	chr6:150664117..150665830-chr6:150669653..150671786,2	K562	blood:
45	chr6:150595217..150598289-chr6:150598347..150601921,4	K562	blood:
46	chr6:150679855..150682122-chr6:150688615..150690541,2	K562	blood:
47	chr6:150668412..150670441-chr6:150671071..150673551,2	K562	blood:
48	chr6:150614780..150617065-chr6:150622253..150624530,2	K562	blood:
49	chr6:150652538..150654492-chr6:150655790..150657493,2	K562	blood:
50	chr6:150401082..150403253-chr6:150656281..150658165,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP1R14C-1	chr6:150612026-150612202	XLOC_005502
2	lnc-IYD-3	chr6:150668413-150668936	l_3297_chr6:150632564-150635742_testes
3	lnc-PPP1R14C-1	chr6:150615916-150616896	XLOC_005502
4	lnc-PPP1R14C-1	chr6:150590872-150591106	XLOC_005502
5	lnc-IYD-3	chr6:150635552-150635742	l_3297_chr6:150632564-150635742_testes
6	lnc-PPP1R14C-1	chr6:150593859-150593991	XLOC_005502
7	lnc-ULBP3-4	chr6:150705443-150706256	NONHSAT115540
8	lnc-PPP1R14C-1	chr6:150626922-150627165	NONHSAT115535
9	lnc-PPP1R14C-1	chr6:150615916-150616003	NONHSAT115535
10	lnc-IYD-3	chr6:150657609-150657837	l_3297_chr6:150632564-150635742_testes
11	lnc-PPP1R14C-1	chr6:150593859-150594048	NONHSAT115534
12	lnc-PPP1R14C-1	chr6:150590912-150591106	NONHSAT115534
13	lnc-PPP1R14C-1	chr6:150615916-150616004	XLOC_005502
14	lnc-PPP1R14C-1	chr6:150590907-150591106	XLOC_005502
15	lnc-IYD-3	chr6:150632565-150632799	l_3297_chr6:150632564-150635742_testes
16	lnc-PPP1R14C-1	chr6:150590912-150591106	NONHSAT115535

No data

Variant related genes	Relation type
IYD	TF binding region
RNU4-7P	TF binding region
SSR1P1	TF binding region
IYD	CpG island
RNU4-7P	CpG island
SSR1P1	CpG island
ENSG00000220598	chromatin interactions
ENSG00000009765	chromatin interactions
ENSG00000201628	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000120254	chromatin interactions
CDC27	miRNA target sites
CDC25B	miRNA target sites

Extended variants
information (count: 5761 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:5761 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17079528	chr6:150581193-150581194	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188855403	chr6:150581202-150581203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570417412	chr6:150581252-150581253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs57362276	chr6:150581287-150581288	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs72995381	chr6:150581380-150581381	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs192878673	chr6:150581392-150581393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566137925	chr6:150581404-150581405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375575033	chr6:150581416-150581417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185813531	chr6:150581424-150581425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559180856	chr6:150581462-150581463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533210036	chr6:150581478-150581479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs115897326	chr6:150581482-150581483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574783264	chr6:150581548-150581549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs34893981	chr6:150581605-150581606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs397888197	chr6:150581609-150581610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs9322255	chr6:150581610-150581611	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs189372629	chr6:150581611-150581612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371017611	chr6:150581629-150581630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546388755	chr6:150581673-150581674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540994462	chr6:150581684-150581685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115155295	chr6:150581688-150581689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569835401	chr6:150581723-150581724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191505717	chr6:150581765-150581766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541599690	chr6:150581846-150581847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370189692	chr6:150581851-150581852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560725964	chr6:150581874-150581875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs79967176	chr6:150581970-150581971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs7454486	chr6:150581992-150581993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375404682	chr6:150582029-150582030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs9480096	chr6:150582038-150582039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115750184	chr6:150582075-150582076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536361479	chr6:150582111-150582112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570380161	chr6:150582141-150582142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs9480097	chr6:150582191-150582192	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146977173	chr6:150582198-150582199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369767541	chr6:150582201-150582202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373363775	chr6:150582202-150582203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs199959451	chr6:150582216-150582217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563422426	chr6:150582229-150582230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373879573	chr6:150582287-150582288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs546752757	chr6:150582295-150582296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs11417501	chr6:150582296-150582297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs398003053	chr6:150582297-150582298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566585959	chr6:150582301-150582302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535110897	chr6:150582326-150582327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554814490	chr6:150582358-150582359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568573456	chr6:150582377-150582378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552124210	chr6:150582385-150582386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534311331	chr6:150582406-150582407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188709106	chr6:150582425-150582426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Developmental delay	21147756	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1082 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150574800-150590800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:150577400-150585200	Weak transcription	Right Ventricle	heart
3	chr6:150577400-150585400	Weak transcription	Left Ventricle	heart
4	chr6:150577400-150588200	Weak transcription	Psoas Muscle	Psoas
5	chr6:150578000-150589000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr6:150578400-150588000	Weak transcription	NH-A	brain
7	chr6:150579200-150587600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr6:150579400-150584200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:150579400-150587200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr6:150579400-150587200	Weak transcription	NHEK	skin
11	chr6:150580200-150581600	Enhancers	K562	blood
12	chr6:150580400-150590800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr6:150580600-150586000	Enhancers	Fetal Heart	heart
14	chr6:150580600-150587000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr6:150581600-150584200	Weak transcription	K562	blood
16	chr6:150582000-150582200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:150582200-150583200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:150583000-150583600	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr6:150583000-150583600	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr6:150583200-150583600	Enhancers	H1 Cell Line	embryonic stem cell
21	chr6:150583200-150583600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:150583200-150583600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr6:150583200-150583600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr6:150583200-150583800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr6:150583200-150584600	Enhancers	Fetal Lung	lung
26	chr6:150583400-150583800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr6:150583400-150583800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr6:150583600-150606800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:150583800-150591000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr6:150584200-150584600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr6:150584200-150584800	Enhancers	K562	blood
32	chr6:150584200-150585000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr6:150584200-150586200	Enhancers	Primary T cells fromperipheralblood	blood
34	chr6:150584600-150586200	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
35	chr6:150584600-150589200	Weak transcription	Fetal Lung	lung
36	chr6:150584800-150585000	Enhancers	Primary B cells from peripheral blood	blood
37	chr6:150584800-150585200	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr6:150584800-150585400	Enhancers	Spleen	Spleen
39	chr6:150584800-150587400	Weak transcription	K562	blood
40	chr6:150585000-150585200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr6:150585000-150585200	Bivalent Enhancer	Placenta	Placenta
42	chr6:150585000-150585600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr6:150585000-150585600	Bivalent Enhancer	Esophagus	oesophagus
44	chr6:150585000-150585800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
45	chr6:150585200-150585400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr6:150585200-150586200	Enhancers	Right Ventricle	heart
47	chr6:150585400-150585600	Enhancers	Left Ventricle	heart
48	chr6:150585400-150586000	Weak transcription	Spleen	Spleen
49	chr6:150585600-150585800	Enhancers	Esophagus	oesophagus
50	chr6:150585600-150586000	Enhancers	Primary T helper cells fromperipheralblood	blood

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