Variant report

Variant	nsv508246
Chromosome Location	chr3:135922023-136038622
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1465)
CpG islands
(count:1407)
Chromatin interactive
region (count:81)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:135967815-135968358	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:135985418-135985683	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:135932164-135932533	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:135969875-135970236	K562	blood:	n/a	n/a
5	ARID3A	chr3:135968840-135969614	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:135974327-135974914	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:135969896-135970500	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:135956954-135957417	HepG2	liver:	n/a	n/a
9	ATF2	chr3:135968916-135969955	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr3:135969099-135969587	GM12878	blood:	n/a	n/a
11	ATF2	chr3:135968769-135969758	GM12878	blood:	n/a	n/a
12	ATF3	chr3:135969091-135969326	K562	blood:	n/a	n/a
13	BACH1	chr3:136015869-136016121	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr3:135996778-135996977	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:135969046-135969547	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr3:135985387-135985636	GM12878	blood:	n/a	n/a
17	BATF	chr3:135989078-135989394	GM12878	blood:	n/a	n/a
18	BATF	chr3:135989055-135989365	GM12878	blood:	n/a	n/a
19	BATF	chr3:135985265-135985612	GM12878	blood:	n/a	n/a
20	BCLAF1	chr3:135969731-135970321	GM12878	blood:	n/a	chr3:135970232-135970241
21	BCLAF1	chr3:135968732-135969383	GM12878	blood:	n/a	n/a
22	BHLHE40	chr3:135969035-135970296	HepG2	liver:	n/a	chr3:135969109-135969125
23	BHLHE40	chr3:135968891-135970408	K562	blood:	n/a	chr3:135969109-135969125
24	BHLHE40	chr3:135968908-135970335	GM12878	blood:	n/a	chr3:135969109-135969125
25	BHLHE40	chr3:135974568-135974795	HepG2	liver:	n/a	n/a
26	BRCA1	chr3:135969027-135969471	HepG2	liver:	n/a	n/a
27	BRCA1	chr3:135968861-135969794	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr3:135967491-135967602	H1-hESC	embryonic stem cell:	n/a	n/a
29	CBX3	chr3:135968981-135969557	K562	blood:	n/a	n/a
30	CBX3	chr3:135937905-135938316	K562	blood:	n/a	n/a
31	CBX3	chr3:135969740-135970225	K562	blood:	n/a	n/a
32	CBX3	chr3:135999862-136000401	K562	blood:	n/a	n/a
33	CBX3	chr3:135937984-135938201	K562	blood:	n/a	n/a
34	CBX3	chr3:135969694-135970536	K562	blood:	n/a	n/a
35	CBX3	chr3:135969000-135969321	K562	blood:	n/a	n/a
36	CCNT2	chr3:135969903-135970290	K562	blood:	n/a	n/a
37	CCNT2	chr3:135968969-135969561	K562	blood:	n/a	n/a
38	CEBPB	chr3:135934593-135934813	K562	blood:	n/a	chr3:135934696-135934707
39	CEBPB	chr3:135968439-135969426	K562	blood:	n/a	chr3:135968595-135968606
40	CEBPB	chr3:136028538-136028621	H1-hESC	embryonic stem cell:	n/a	chr3:136028594-136028605
41	CEBPB	chr3:136028545-136028738	HepG2	liver:	n/a	chr3:136028594-136028605
42	CEBPB	chr3:135970384-135970762	HepG2	liver:	n/a	chr3:135970665-135970676 chr3:135970576-135970587 chr3:135970574-135970587 chr3:135970574-135970587 chr3:135970574-135970585
43	CEBPB	chr3:135970370-135970714	HepG2	liver:	n/a	chr3:135970665-135970676 chr3:135970576-135970587 chr3:135970574-135970587 chr3:135970574-135970587 chr3:135970574-135970585
44	CEBPB	chr3:135969081-135969247	HepG2	liver:	n/a	n/a
45	CEBPB	chr3:135954513-135954772	HepG2	liver:	n/a	n/a
46	CEBPB	chr3:135970397-135970755	HepG2	liver:	n/a	chr3:135970665-135970676 chr3:135970576-135970587 chr3:135970574-135970587 chr3:135970574-135970587 chr3:135970574-135970585
47	CEBPB	chr3:135970331-135970764	K562	blood:	n/a	chr3:135970665-135970676 chr3:135970576-135970587 chr3:135970574-135970587 chr3:135970574-135970587 chr3:135970574-135970585
48	CEBPB	chr3:135968496-135968709	HepG2	liver:	n/a	chr3:135968595-135968606
49	CEBPB	chr3:135974492-135974848	HepG2	liver:	n/a	n/a
50	CEBPB	chr3:135968477-135968772	H1-hESC	embryonic stem cell:	n/a	chr3:135968595-135968606

(count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:135996211-135996261	AG04450	lung:	fetal
2	chr3:135968952-135969002	HAEpiC	amniotic membrane:	n/a
3	chr3:136002143-136002193	GM19239	blood:	n/a
4	chr3:135969063-135969113	GM12891	blood:	n/a
5	chr3:135996211-135996261	AG04450	lung:	fetal
6	chr3:135968952-135969002	HAEpiC	amniotic membrane:	n/a
7	chr3:136002143-136002193	GM19239	blood:	n/a
8	chr3:135969063-135969113	GM12891	blood:	n/a
9	chr3:135972373-135972423	ECC-1	luminal epithelium:	n/a
10	chr3:135969981-135970031	SK-N-MC	brain:	n/a
11	chr3:135969387-135969437	HCM	heart:	n/a
12	chr3:135967896-135967946	RPTEC	kidney:	n/a
13	chr3:135969041-135969091	AG10803	skin:	n/a
14	chr3:135996211-135996261	A549	lung:	n/a
15	chr3:135969116-135969166	SAEC	small airway:	n/a
16	chr3:135969041-135969091	PFSK-1	brain:	n/a
17	chr3:135969136-135969186	BE2_C	brain:	n/a
18	chr3:135969958-135970008	NH-A	brain:	n/a
19	chr3:135956534-135956584	GM06990	blood:	n/a
20	chr3:135969733-135969783	GM12892	blood:	n/a
21	chr3:135969063-135969113	HCF	heart:	n/a
22	chr3:135969053-135969103	GM12892	blood:	n/a
23	chr3:136002143-136002193	IMR90	lung:	fetal
24	chr3:135969136-135969186	T-47D	breast:	n/a
25	chr3:135967896-135967946	Jurkat	blood:	n/a
26	chr3:135957815-135957865	SK-N-SH_RA	brain:	n/a
27	chr3:135969116-135969166	HL-60	blood:	n/a
28	chr3:135969063-135969113	NH-A	brain:	n/a
29	chr3:135969043-135969093	HIPEpiC	eye:	n/a
30	chr3:135969958-135970008	AG09319	gingival:	n/a
31	chr3:135969053-135969103	BE2_C	brain:	n/a
32	chr3:135996211-135996261	RPTEC	kidney:	n/a
33	chr3:135967896-135967946	SK-N-SH_RA	brain:	n/a
34	chr3:135957815-135957865	IMR90	lung:	fetal
35	chr3:135969387-135969437	AG09319	gingival:	n/a
36	chr3:135972373-135972423	HNPCEpiC	eye:	n/a
37	chr3:135996211-135996261	T-47D	breast:	n/a
38	chr3:135969041-135969091	AoSMC	blood vessel:	n/a
39	chr3:136016212-136016262	HEEpiC	esophagus:	n/a
40	chr3:135954970-135955020	IMR90	lung:	fetal
41	chr3:135969053-135969103	MCF10A-Er-Src	breast:	n/a
42	chr3:135967896-135967946	HL-60	blood:	n/a
43	chr3:136016212-136016262	NT2-D1	testis:	n/a
44	chr3:135969556-135969606	GM12892	blood:	n/a
45	chr3:135956534-135956584	HCPEpiC	choroid plexus:	n/a
46	chr3:135969041-135969091	NB4	blood:	n/a
47	chr3:135969981-135970031	PANC-1	pancreas:	n/a
48	chr3:135969958-135970008	AG04449	skin:	fetal
49	chr3:135957815-135957865	GM19239	blood:	n/a
50	chr3:135969981-135970031	MCF-7	breast:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:135913590..135917736-chr3:135926083..135932261,5	MCF-7	breast:
2	chr3:136024388..136025351-chr3:136470886..136471672,6	MCF-7	breast:
3	chr3:135978505..135981736-chr3:135997267..135999290,3	K562	blood:
4	chr3:135915088..135917295-chr3:135928365..135931096,4	K562	blood:
5	chr3:135914359..135917940-chr3:135918665..135923350,9	MCF-7	breast:
6	chr3:135968510..135970353-chr3:135983958..135985710,2	K562	blood:
7	chr3:135913368..135917347-chr3:136002399..136005146,3	MCF-7	breast:
8	chr3:135967895..135971293-chr3:135973278..135977937,5	MCF-7	breast:
9	chr3:135953105..135954994-chr3:135955237..135956991,2	MCF-7	breast:
10	chr3:135914895..135917760-chr3:135953587..135955253,2	MCF-7	breast:
11	chr3:135967695..135971650-chr3:135990633..135993789,4	MCF-7	breast:
12	chr3:135968568..135972532-chr3:135974380..135977728,5	K562	blood:
13	chr3:135793633..135795378-chr3:136008278..136010126,2	MCF-7	breast:
14	chr3:135953105..135954994-chr3:135955237..135956991,2	MCF-7	breast:
15	chr3:135914453..135916703-chr3:135953216..135954828,2	K562	blood:
16	chr3:135914663..135917728-chr3:135920669..135925255,5	MCF-7	breast:
17	chr3:135967729..135968689-chr3:136062451..136063319,2	MCF-7	breast:
18	chr3:135913662..135918303-chr3:135918792..135923600,7	K562	blood:
19	chr3:135967895..135971293-chr3:135973278..135977937,5	MCF-7	breast:
20	chr3:135913637..135916357-chr3:136011519..136014362,3	MCF-7	breast:
21	chr3:135914645..135915534-chr3:135968907..135969695,2	Hela-S3	cervix:
22	chr3:135913726..135915628-chr3:135923532..135925229,2	MCF-7	breast:
23	chr3:135974598..135977486-chr3:135979875..135981480,2	MCF-7	breast:
24	chr3:135914260..135917175-chr3:135955428..135961207,5	MCF-7	breast:
25	chr3:135913308..135916970-chr3:135973705..135976198,3	K562	blood:
26	chr3:135968568..135972532-chr3:135974380..135977728,5	K562	blood:
27	chr3:135960116..135965252-chr3:135965591..135969591,6	MCF-7	breast:
28	chr3:135928475..135930111-chr3:135931628..135934340,2	K562	blood:
29	chr3:135912206..135917353-chr3:135967047..135972220,20	MCF-7	breast:
30	chr3:135916249..135918777-chr3:135964014..135966844,3	K562	blood:
31	chr3:135968816..135970584-chr3:136001826..136004051,2	MCF-7	breast:
32	chr3:136010183..136011753-chr3:136025540..136027566,2	K562	blood:
33	chr3:135954969..135958105-chr3:135968052..135971178,3	MCF-7	breast:
34	chr3:136010183..136011753-chr3:136025540..136027566,2	K562	blood:
35	chr3:135914067..135916251-chr3:135996323..135999070,2	MCF-7	breast:
36	chr3:135914289..135916961-chr3:135976114..135978100,2	MCF-7	breast:
37	chr3:135914058..135916023-chr3:135977800..135980119,2	MCF-7	breast:
38	chr3:135956487..135958246-chr3:135959617..135962122,2	MCF-7	breast:
39	chr3:135912197..135914023-chr3:135984563..135987150,2	MCF-7	breast:
40	chr3:135929618..135932203-chr3:135951944..135954084,2	K562	blood:
41	chr3:136033614..136036060-chr3:136051639..136053164,2	MCF-7	breast:
42	chr3:136030321..136031240-chrX:106919908..106920687,2	NB4	blood:
43	chr3:135955194..135957382-chr3:135967889..135969974,2	MCF-7	breast:
44	chr3:135928475..135930111-chr3:135931628..135934340,2	K562	blood:
45	chr3:135915739..135918112-chr3:135931092..135933753,3	K562	blood:
46	chr3:135968107..135969967-chr3:136470513..136472370,2	MCF-7	breast:
47	chr3:136012746..136014476-chr3:136025907..136027620,2	K562	blood:
48	chr3:136025488..136027450-chr3:136031580..136034154,2	K562	blood:
49	chr3:135962309..135964961-chr3:135967588..135970580,2	MCF-7	breast:
50	chr3:135915695..135917970-chr3:135924534..135927537,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCCB-1	chr3:135934796-135934839	NONHSAT092275
2	lnc-PCCB-1	chr3:135955807-135955888	NONHSAT092275
3	lnc-PCCB-1	chr3:135944465-135944567	NONHSAT092275

No data

Variant related genes	Relation type
ENSG00000244740	TF binding region
PCCB	TF binding region
ENSG00000244740	CpG island
PCCB	CpG island
ENSG00000261758	chromatin interactions
ENSG00000124635	chromatin interactions
ENSG00000110321	chromatin interactions
ENSG00000118007	chromatin interactions
ENSG00000114054	chromatin interactions
ENSG00000246308	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000073711	chromatin interactions
ENSG00000174579	chromatin interactions

Extended variants
information (count: 3962 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:3962 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551884013	chr3:135922023-135922024	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs565752216	chr3:135922056-135922057	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs147172134	chr3:135922099-135922100	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs370223265	chr3:135922147-135922148	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs575036755	chr3:135922183-135922184	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs537697397	chr3:135922213-135922214	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs188311815	chr3:135922223-135922224	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs73865203	chr3:135922243-135922244	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs542314738	chr3:135922244-135922245	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs560813596	chr3:135922274-135922275	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191536276	chr3:135922292-135922293	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs559917961	chr3:135922372-135922373	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs573275234	chr3:135922452-135922453	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs35972738	chr3:135922458-135922459	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs182674768	chr3:135922460-135922461	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs562066665	chr3:135922497-135922498	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs529962965	chr3:135922547-135922548	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs368157785	chr3:135922550-135922551	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs186951978	chr3:135922557-135922558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs138619645	chr3:135922590-135922591	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs142703150	chr3:135922644-135922645	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs551945179	chr3:135922662-135922663	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs565685986	chr3:135922694-135922695	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534668430	chr3:135922762-135922763	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs191273189	chr3:135922768-135922769	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs77076019	chr3:135922811-135922812	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs527704560	chr3:135922822-135922823	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs74559125	chr3:135922823-135922824	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs79805752	chr3:135922826-135922827	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs79407574	chr3:135922843-135922844	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs537762545	chr3:135922853-135922854	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs184933598	chr3:135922860-135922861	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs577593624	chr3:135922871-135922872	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs542832587	chr3:135922882-135922883	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs188955959	chr3:135922893-135922894	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs367720989	chr3:135922911-135922912	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs192939099	chr3:135922952-135922953	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs139984612	chr3:135922962-135922963	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs531827035	chr3:135922994-135922995	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs573258144	chr3:135923003-135923004	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs542275896	chr3:135923072-135923073	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs561964871	chr3:135923073-135923074	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs575265475	chr3:135923104-135923105	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs149863052	chr3:135923145-135923146	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs545676947	chr3:135923157-135923158	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs563283620	chr3:135923164-135923165	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs113256029	chr3:135923173-135923174	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532271781	chr3:135923197-135923198	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs372089364	chr3:135923210-135923211	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs545596926	chr3:135923241-135923242	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18511947	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:2642 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:135916200-135922600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:135917200-135922400	Weak transcription	HUVEC	blood vessel
3	chr3:135922000-135923400	Enhancers	HepG2	liver
4	chr3:135922600-135922800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr3:135923400-135931400	Weak transcription	HepG2	liver
6	chr3:135924400-135927000	Enhancers	Brain Germinal Matrix	brain
7	chr3:135924800-135927200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr3:135925400-135926200	Enhancers	Fetal Brain Male	brain
9	chr3:135925800-135926400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr3:135926000-135926200	Enhancers	Brain Angular Gyrus	brain
11	chr3:135926000-135926200	Enhancers	Brain Cingulate Gyrus	brain
12	chr3:135926000-135926400	Enhancers	Brain Hippocampus Middle	brain
13	chr3:135926000-135926400	Enhancers	Fetal Muscle Leg	muscle
14	chr3:135926000-135927000	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr3:135926200-135926400	Enhancers	Brain Anterior Caudate	brain
16	chr3:135926200-135926600	Flanking Active TSS	Brain Angular Gyrus	brain
17	chr3:135926200-135926600	Weak transcription	Fetal Brain Male	brain
18	chr3:135926200-135927000	Enhancers	Brain Substantia Nigra	brain
19	chr3:135926400-135926800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr3:135926400-135926800	Flanking Active TSS	Brain Anterior Caudate	brain
21	chr3:135926400-135926800	Flanking Active TSS	Brain Hippocampus Middle	brain
22	chr3:135926600-135927000	Enhancers	Brain Angular Gyrus	brain
23	chr3:135926600-135927000	Enhancers	Fetal Brain Male	brain
24	chr3:135926800-135927000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr3:135926800-135927000	Enhancers	Brain Anterior Caudate	brain
26	chr3:135926800-135927000	Enhancers	Brain Cingulate Gyrus	brain
27	chr3:135926800-135927000	Bivalent Enhancer	Brain Hippocampus Middle	brain
28	chr3:135926800-135927000	Enhancers	Fetal Muscle Leg	muscle
29	chr3:135928600-135929000	Enhancers	NHDF-Ad	bronchial
30	chr3:135928600-135929200	Enhancers	NHLF	lung
31	chr3:135928600-135929400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr3:135928600-135929400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr3:135928600-135929400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr3:135928800-135929000	Enhancers	NH-A	brain
35	chr3:135928800-135929200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr3:135928800-135929200	Enhancers	A549	lung
37	chr3:135930400-135930800	Enhancers	K562	blood
38	chr3:135930800-135934200	Enhancers	Liver	Liver
39	chr3:135931400-135933400	Enhancers	HepG2	liver
40	chr3:135941600-135941800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr3:135941600-135942200	Enhancers	Duodenum Mucosa	Duodenum
42	chr3:135941600-135942600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr3:135941600-135942600	Enhancers	Muscle Satellite Cultured Cells	--
44	chr3:135942000-135942600	Enhancers	HSMMtube	muscle
45	chr3:135942200-135942600	Flanking Active TSS	Duodenum Mucosa	Duodenum
46	chr3:135951200-135951800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr3:135952200-135952600	Enhancers	GM12878-XiMat	blood
48	chr3:135953800-135955400	Enhancers	Liver	Liver
49	chr3:135954400-135955400	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr3:135954600-135954800	Active TSS	iPS-20b Cell Line	embryonic stem cell

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