Variant report

Variant	nsv1015360
Chromosome Location	chr6:149609804-149649982
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:149638387-149638753	K562	blood:	n/a	n/a
2	ARID3A	chr6:149638494-149638818	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:149634272-149634424	K562	blood:	n/a	n/a
4	ARID3A	chr6:149610606-149610624	HepG2	liver:	n/a	n/a
5	ATF2	chr6:149640165-149641065	GM12878	blood:	n/a	n/a
6	ATF2	chr6:149639222-149640982	GM12878	blood:	n/a	n/a
7	ATF2	chr6:149614393-149614761	GM12878	blood:	n/a	n/a
8	BATF	chr6:149628106-149628385	GM12878	blood:	n/a	chr6:149628265-149628276
9	BATF	chr6:149614424-149614700	GM12878	blood:	n/a	chr6:149614529-149614540 chr6:149614530-149614540
10	BATF	chr6:149614452-149614659	GM12878	blood:	n/a	chr6:149614529-149614540 chr6:149614530-149614540
11	BCL3	chr6:149638360-149639002	GM12878	blood:	n/a	chr6:149638863-149638876 chr6:149638416-149638429 chr6:149638655-149638668 chr6:149638658-149638671 chr6:149638660-149638669 chr6:149638441-149638454
12	BCLAF1	chr6:149637776-149638885	GM12878	blood:	n/a	chr6:149638863-149638876 chr6:149638416-149638429 chr6:149638127-149638136 chr6:149638655-149638668 chr6:149638658-149638671 chr6:149638660-149638669 chr6:149638240-149638249 chr6:149638441-149638454
13	BCLAF1	chr6:149639540-149640584	GM12878	blood:	n/a	chr6:149639598-149639607 chr6:149640392-149640401 chr6:149639540-149639549 chr6:149640035-149640042
14	BHLHE40	chr6:149639174-149639612	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:149637930-149638962	GM12878	blood:	n/a	chr6:149638614-149638630 chr6:149638624-149638640 chr6:149638866-149638882 chr6:149638444-149638460 chr6:149638860-149638876 chr6:149638863-149638879
16	BHLHE40	chr6:149637876-149638744	K562	blood:	n/a	chr6:149638614-149638630 chr6:149638624-149638640 chr6:149638444-149638460
17	BHLHE40	chr6:149639101-149639377	K562	blood:	n/a	n/a
18	BHLHE40	chr6:149640773-149640966	GM12878	blood:	n/a	n/a
19	BRCA1	chr6:149638295-149638834	GM12878	blood:	n/a	n/a
20	BRCA1	chr6:149639146-149639346	GM12878	blood:	n/a	n/a
21	BRCA1	chr6:149639201-149639305	HepG2	liver:	n/a	n/a
22	BRCA1	chr6:149639172-149639297	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr6:149639161-149639318	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr6:149638271-149638845	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr6:149638136-149638837	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr6:149638441-149638880	HepG2	liver:	n/a	n/a
27	CBX3	chr6:149638290-149638781	K562	blood:	n/a	n/a
28	CCNT2	chr6:149637982-149639574	K562	blood:	n/a	chr6:149639539-149639548 chr6:149638900-149638909 chr6:149639363-149639372 chr6:149639413-149639422 chr6:149638895-149638904 chr6:149638505-149638514
29	CCNT2	chr6:149642149-149642279	K562	blood:	n/a	n/a
30	CEBPB	chr6:149640146-149640486	IMR90	lung:	n/a	chr6:149640324-149640335 chr6:149640325-149640336 chr6:149640324-149640337
31	CEBPB	chr6:149632432-149632826	K562	blood:	n/a	chr6:149632618-149632629
32	CEBPB	chr6:149624655-149624887	H1-hESC	embryonic stem cell:	n/a	chr6:149624779-149624790
33	CEBPB	chr6:149632449-149632807	A549	lung:	n/a	chr6:149632618-149632629
34	CEBPB	chr6:149624734-149624917	A549	lung:	n/a	chr6:149624779-149624790
35	CEBPB	chr6:149632439-149632764	Hela-S3	cervix:	n/a	chr6:149632618-149632629
36	CEBPB	chr6:149632381-149632789	MCF-7	breast:	n/a	chr6:149632618-149632629
37	CEBPB	chr6:149640170-149640505	HepG2	liver:	n/a	chr6:149640324-149640335 chr6:149640325-149640336 chr6:149640324-149640337
38	CEBPB	chr6:149624638-149624972	HepG2	liver:	n/a	chr6:149624779-149624790
39	CEBPB	chr6:149632425-149632813	K562	blood:	n/a	chr6:149632618-149632629
40	CEBPB	chr6:149624657-149624941	IMR90	lung:	n/a	chr6:149624779-149624790
41	CEBPB	chr6:149640164-149640479	A549	lung:	n/a	chr6:149640324-149640335 chr6:149640325-149640336 chr6:149640324-149640337
42	CEBPB	chr6:149634293-149634440	K562	blood:	n/a	n/a
43	CEBPB	chr6:149632371-149632816	A549	lung:	n/a	chr6:149632618-149632629
44	CEBPB	chr6:149632535-149632743	K562	blood:	n/a	chr6:149632618-149632629
45	CEBPB	chr6:149632409-149632699	HepG2	liver:	n/a	chr6:149632618-149632629
46	CEBPB	chr6:149640114-149640532	MCF-7	breast:	n/a	chr6:149640324-149640335 chr6:149640325-149640336 chr6:149640324-149640337
47	CEBPB	chr6:149632435-149632815	HepG2	liver:	n/a	chr6:149632618-149632629
48	CEBPB	chr6:149634009-149634487	K562	blood:	n/a	n/a
49	CEBPB	chr6:149632438-149632789	MCF-7	breast:	n/a	chr6:149632618-149632629
50	CEBPB	chr6:149640084-149640531	A549	lung:	n/a	chr6:149640324-149640335 chr6:149640325-149640336 chr6:149640324-149640337

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:149638666-149638716	NH-A	brain:	n/a
2	chr6:149638666-149638716	NH-A	brain:	n/a
3	chr6:149639693-149639743	ECC-1	luminal epithelium:	n/a
4	chr6:149638666-149638716	PANC-1	pancreas:	n/a
5	chr6:149638382-149638432	HCM	heart:	n/a
6	chr6:149639041-149639091	AoSMC	blood vessel:	n/a
7	chr6:149639101-149639151	NHBE	bronchial:	n/a
8	chr6:149634176-149634226	HL-60	blood:	n/a
9	chr6:149634176-149634226	MCF-7	breast:	n/a
10	chr6:149637881-149637931	HEEpiC	esophagus:	n/a
11	chr6:149638041-149638091	SK-N-SH_RA	brain:	n/a
12	chr6:149638666-149638716	Hepatocyte	liver:	n/a
13	chr6:149634176-149634226	SK-N-SH_RA	brain:	n/a
14	chr6:149638666-149638716	GM06990	blood:	n/a
15	chr6:149638666-149638716	ProgFib	skin:	n/a
16	chr6:149639101-149639151	NH-A	brain:	n/a
17	chr6:149638041-149638091	SK-N-MC	brain:	n/a
18	chr6:149637881-149637931	LNCaP	prostate:	n/a
19	chr6:149634176-149634226	HCT-116	colon:	n/a
20	chr6:149638666-149638716	GM12878	blood:	n/a
21	chr6:149638666-149638716	RPTEC	kidney:	n/a
22	chr6:149638041-149638091	HNPCEpiC	eye:	n/a
23	chr6:149639693-149639743	HNPCEpiC	eye:	n/a
24	chr6:149639041-149639091	HMEC	breast:	n/a
25	chr6:149638382-149638432	HPAEpiC	pulmonary alveolar:	n/a
26	chr6:149639101-149639151	PrEC	prostate:	n/a
27	chr6:149638666-149638716	Jurkat	blood:	n/a
28	chr6:149638382-149638432	NHBE	bronchial:	n/a
29	chr6:149639101-149639151	HRCEpiC	kidney:	n/a
30	chr6:149639041-149639091	ProgFib	skin:	n/a
31	chr6:149638666-149638716	AG04449	skin:	fetal
32	chr6:149639693-149639743	Hela-S3	cervix:	n/a
33	chr6:149638666-149638716	LNCaP	prostate:	n/a
34	chr6:149639693-149639743	H1-hESC	embryonic stem cell:	embryo
35	chr6:149638382-149638432	HepG2	liver:	n/a
36	chr6:149639101-149639151	GM06990	blood:	n/a
37	chr6:149639041-149639091	BJ	skin:	n/a
38	chr6:149639041-149639091	GM12878	blood:	n/a
39	chr6:149638041-149638091	AG10803	skin:	n/a
40	chr6:149639693-149639743	SK-N-MC	brain:	n/a
41	chr6:149639041-149639091	HPAEpiC	pulmonary alveolar:	n/a
42	chr6:149639693-149639743	Caco-2	colon:	n/a
43	chr6:149638382-149638432	BJ	skin:	n/a
44	chr6:149638382-149638432	SKMC	muscle:	n/a
45	chr6:149638041-149638091	HEEpiC	esophagus:	n/a
46	chr6:149634176-149634226	HAEpiC	amniotic membrane:	n/a
47	chr6:149638041-149638091	PFSK-1	brain:	n/a
48	chr6:149637881-149637931	RPTEC	kidney:	n/a
49	chr6:149638666-149638716	NHDF-neo	bronchial:	n/a
50	chr6:149639693-149639743	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:149613923..149616673-chr6:149638144..149639950,3	K562	blood:
2	chr6:149397256..149399835-chr6:149636593..149638648,2	MCF-7	breast:
3	chr6:149617347..149620525-chr6:149621010..149624915,3	MCF-7	breast:
4	chr6:149617752..149621421-chr6:149622523..149625158,3	K562	blood:
5	chr6:149351823..149355344-chr6:149638842..149641991,4	MCF-7	breast:
6	chr6:149352699..149354339-chr6:149614448..149616568,2	MCF-7	breast:
7	chr6:149617752..149621421-chr6:149622523..149625158,3	K562	blood:
8	chr6:149535644..149537986-chr6:149647515..149649040,2	K562	blood:
9	chr6:149625453..149629470-chr6:149636058..149640474,5	MCF-7	breast:
10	chr6:149409902..149411675-chr6:149636224..149638635,2	K562	blood:
11	chr6:149609220..149611786-chr6:149613185..149616035,2	MCF-7	breast:
12	chr6:149610717..149612656-chr6:149617526..149619312,2	MCF-7	breast:
13	chr6:149615967..149618334-chr6:149622584..149624588,2	K562	blood:
14	chr6:149628297..149630405-chr6:149634848..149636468,2	K562	blood:
15	chr6:149538892..149540721-chr6:149638148..149641111,2	MCF-7	breast:
16	chr6:149613923..149616421-chr6:149638170..149639950,2	K562	blood:
17	chr6:149638704..149639215-chr9:132388273..132388852,2	Hela-S3	cervix:
18	chr6:149648554..149650974-chr6:149651371..149654134,3	K562	blood:
19	chr6:149618848..149621708-chr6:149625417..149626920,2	K562	blood:
20	chr6:149644563..149647339-chr6:149647427..149650792,4	K562	blood:
21	chr6:149409350..149410995-chr6:149644588..149646898,2	K562	blood:
22	chr6:149591541..149593325-chr6:149634432..149636846,2	MCF-7	breast:
23	chr6:149564226..149566619-chr6:149641623..149643146,2	K562	blood:
24	chr6:149629573..149635646-chr6:149637142..149639783,10	MCF-7	breast:
25	chr6:149643394..149646422-chr6:149647403..149650011,4	K562	blood:
26	chr6:149615967..149618334-chr6:149622584..149624588,2	K562	blood:
27	chr6:149406954..149409794-chr6:149636560..149638477,3	MCF-7	breast:
28	chr6:149414073..149415893-chr6:149615671..149617691,2	MCF-7	breast:
29	chr6:149638315..149640262-chr6:149865472..149868393,2	K562	blood:
30	chr6:149380086..149382702-chr6:149642964..149645035,2	MCF-7	breast:
31	chr6:149609220..149611786-chr6:149613185..149616035,2	MCF-7	breast:
32	chr6:149636994..149642058-chr6:149649092..149655125,9	MCF-7	breast:
33	chr6:149617737..149619695-chr6:149633576..149636215,2	MCF-7	breast:
34	chr6:149620609..149622948-chr6:149640554..149642656,2	K562	blood:
35	chr6:149612855..149615541-chr6:149636772..149639074,2	MCF-7	breast:
36	chr6:149625453..149629470-chr6:149636058..149640474,5	MCF-7	breast:
37	chr6:149349779..149353985-chr6:149637379..149639962,5	MCF-7	breast:
38	chr6:149619251..149620814-chr6:149634430..149637387,2	K562	blood:
39	chr12:32832084..32832584-chr6:149638471..149638974,2	NB4	blood:
40	chr6:149557890..149560221-chr6:149637001..149638608,2	MCF-7	breast:
41	chr6:149643394..149646422-chr6:149647403..149650011,4	K562	blood:
42	chr6:149635359..149638022-chr6:149700186..149702826,2	K562	blood:
43	chr6:149617347..149620525-chr6:149621010..149624915,3	MCF-7	breast:
44	chr6:149516981..149518503-chr6:149637137..149638798,2	MCF-7	breast:
45	chr6:149619314..149622625-chr6:149634430..149636159,3	K562	blood:
46	chr6:149646598..149650161-chr6:149650268..149655691,6	MCF-7	breast:
47	chr6:149642865..149645034-chr6:149649169..149650874,2	MCF-7	breast:
48	chr4:174090099..174090929-chr6:149638008..149638852,2	NB4	blood:
49	chr6:149636797..149639661-chr6:149663144..149666590,3	K562	blood:
50	chr6:149619314..149622625-chr6:149634430..149636159,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUMO4-4	chr6:149612488-149612780	NONHSAT115495
2	lnc-ZC3H12D-10	chr6:149625243-149625564	NONHSAT115496

Variant related genes	Relation type
RN7SL234P	TF binding region
TAB2	TF binding region
FABP12P1	TF binding region
RN7SL234P	CpG island
TAB2	CpG island
FABP12P1	CpG island
ENSG00000236591	chromatin interactions
ENSG00000225924	chromatin interactions
ENSG00000241391	chromatin interactions
ENSG00000228408	chromatin interactions
ENSG00000148335	chromatin interactions
ENSG00000131013	chromatin interactions
ENSG00000245213	chromatin interactions
ENSG00000087470	chromatin interactions
ENSG00000216265	chromatin interactions
ENSG00000055208	chromatin interactions

Extended variants
information (count: 1507 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1507 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539953285	chr6:149609855-149609856	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs190579992	chr6:149609861-149609862	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs12527657	chr6:149609869-149609870	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs72997896	chr6:149609910-149609911	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs568721062	chr6:149609918-149609919	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs566236476	chr6:149609924-149609925	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs34381803	chr6:149609934-149609935	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs537701553	chr6:149609935-149609936	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs4895783	chr6:149609960-149609961	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs537209144	chr6:149609991-149609992	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs71007938	chr6:149610011-149610012	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs570502719	chr6:149610025-149610026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs193035541	chr6:149610030-149610031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541734680	chr6:149610045-149610046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376973826	chr6:149610062-149610063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs4895784	chr6:149610080-149610081	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs4895785	chr6:149610083-149610084	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs4895786	chr6:149610127-149610128	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs144229083	chr6:149610130-149610131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185776781	chr6:149610160-149610161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564805925	chr6:149610246-149610247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs9498291	chr6:149610247-149610248	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs540201356	chr6:149610274-149610275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114179922	chr6:149610277-149610278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs9498292	chr6:149610290-149610291	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs548808246	chr6:149610297-149610298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs9498293	chr6:149610339-149610340	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs531444354	chr6:149610352-149610353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs114354570	chr6:149610360-149610361	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs571234596	chr6:149610380-149610381	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs533865592	chr6:149610401-149610402	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs188103187	chr6:149610402-149610403	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs566759251	chr6:149610404-149610405	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs535894099	chr6:149610412-149610413	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs550269053	chr6:149610414-149610415	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs115463683	chr6:149610441-149610442	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs575895032	chr6:149610442-149610443	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs544850492	chr6:149610451-149610452	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs558408767	chr6:149610485-149610486	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs77047585	chr6:149610498-149610499	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs113026356	chr6:149610530-149610531	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs199868463	chr6:149610531-149610532	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs397819582	chr6:149610542-149610543	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs199692647	chr6:149610544-149610545	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs200809421	chr6:149610546-149610547	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs375196230	chr6:149610554-149610555	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs35552421	chr6:149610576-149610577	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs560047946	chr6:149610606-149610607	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs75912148	chr6:149610609-149610610	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs181030447	chr6:149610634-149610635	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1070 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149607000-149610200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr6:149607000-149610400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:149609400-149610000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:149609400-149610200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr6:149609400-149610600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr6:149610200-149611000	Enhancers	HepG2	liver
7	chr6:149610200-149611800	Enhancers	Placenta Amnion	Placenta Amnion
8	chr6:149610400-149612800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:149611000-149611800	Enhancers	Placenta	Placenta
10	chr6:149613200-149615600	Enhancers	NHEK	skin
11	chr6:149613400-149615400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:149614000-149614600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr6:149614000-149614800	Enhancers	HSMM	muscle
14	chr6:149614000-149615000	Enhancers	HMEC	breast
15	chr6:149614000-149615600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr6:149614000-149615600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr6:149614200-149614800	Enhancers	GM12878-XiMat	blood
18	chr6:149614200-149615000	Enhancers	Muscle Satellite Cultured Cells	--
19	chr6:149614400-149614800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:149614600-149615000	Enhancers	HSMMtube	muscle
21	chr6:149624400-149625200	Enhancers	Liver	Liver
22	chr6:149625400-149626000	Enhancers	Brain Anterior Caudate	brain
23	chr6:149625600-149625800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr6:149626000-149626400	Weak transcription	Brain Anterior Caudate	brain
25	chr6:149626200-149627000	Enhancers	Primary hematopoietic stem cells	blood
26	chr6:149626200-149627000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr6:149626200-149627200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr6:149626400-149626600	Enhancers	Brain Anterior Caudate	brain
29	chr6:149626400-149626800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr6:149626400-149627000	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr6:149626400-149627200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr6:149626600-149628200	Weak transcription	Brain Anterior Caudate	brain
33	chr6:149626800-149628000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr6:149627600-149628600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr6:149627800-149628000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr6:149627800-149628200	Enhancers	HSMMtube	muscle
37	chr6:149627800-149628600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr6:149627800-149628600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:149627800-149628800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr6:149627800-149629200	Enhancers	Muscle Satellite Cultured Cells	--
41	chr6:149628000-149628600	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr6:149628000-149628600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr6:149628000-149628800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr6:149628000-149628800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr6:149628000-149629400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr6:149628000-149629400	Enhancers	Osteobl	bone
47	chr6:149628000-149637800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr6:149628200-149628400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:149628200-149628400	Active TSS	A549	lung
50	chr6:149628200-149628600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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