Variant report

Variant	nsv460871
Chromosome Location	chr3:141027614-141074962
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1780)
CpG islands
(count:916)
Chromatin interactive
region (count:151)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1780 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:141030425-141030951	K562	blood:	n/a	n/a
2	ARID3A	chr3:141027527-141027867	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:141071511-141071757	K562	blood:	n/a	n/a
4	ARID3A	chr3:141043266-141043651	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:141031339-141032355	K562	blood:	n/a	n/a
6	ARID3A	chr3:141050625-141051094	K562	blood:	n/a	n/a
7	ARID3A	chr3:141030430-141030957	HepG2	liver:	n/a	n/a
8	ATF1	chr3:141049140-141049468	K562	blood:	n/a	n/a
9	ATF1	chr3:141030406-141031016	K562	blood:	n/a	n/a
10	ATF1	chr3:141050554-141051037	K562	blood:	n/a	n/a
11	ATF1	chr3:141060456-141060728	K562	blood:	n/a	n/a
12	ATF1	chr3:141055964-141056418	K562	blood:	n/a	n/a
13	ATF2	chr3:141055370-141057046	GM12878	blood:	n/a	n/a
14	ATF2	chr3:141050516-141050958	GM12878	blood:	n/a	n/a
15	ATF2	chr3:141046950-141047601	GM12878	blood:	n/a	n/a
16	ATF2	chr3:141050406-141051029	GM12878	blood:	n/a	n/a
17	ATF2	chr3:141030204-141031011	GM12878	blood:	n/a	n/a
18	ATF2	chr3:141030303-141031085	GM12878	blood:	n/a	n/a
19	ATF2	chr3:141047019-141047604	GM12878	blood:	n/a	n/a
20	ATF2	chr3:141055332-141056707	GM12878	blood:	n/a	n/a
21	ATF2	chr3:141030286-141031002	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr3:141050454-141051146	A549	lung:	n/a	n/a
23	ATF3	chr3:141050562-141051070	K562	blood:	n/a	n/a
24	ATF3	chr3:141027470-141027796	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr3:141027383-141027747	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF3	chr3:141050475-141051152	A549	lung:	n/a	n/a
27	ATF3	chr3:141030399-141030894	GM12878	blood:	n/a	n/a
28	ATF3	chr3:141027479-141027749	K562	blood:	n/a	n/a
29	ATF3	chr3:141030281-141030971	K562	blood:	n/a	n/a
30	ATF3	chr3:141050619-141050873	K562	blood:	n/a	n/a
31	BACH1	chr3:141059991-141060222	K562	blood:	n/a	n/a
32	BACH1	chr3:141030341-141030975	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr3:141061543-141061697	K562	blood:	n/a	n/a
34	BACH1	chr3:141031977-141032070	K562	blood:	n/a	n/a
35	BATF	chr3:141047058-141047489	GM12878	blood:	n/a	n/a
36	BATF	chr3:141055437-141056477	GM12878	blood:	n/a	n/a
37	BATF	chr3:141050526-141050969	GM12878	blood:	n/a	chr3:141050752-141050763 chr3:141050753-141050763
38	BATF	chr3:141047041-141047637	GM12878	blood:	n/a	n/a
39	BATF	chr3:141055648-141056463	GM12878	blood:	n/a	n/a
40	BCL11A	chr3:141047098-141047478	GM12878	blood:	n/a	n/a
41	BCL11A	chr3:141047107-141047604	GM12878	blood:	n/a	n/a
42	BCL11A	chr3:141055439-141056387	GM12878	blood:	n/a	chr3:141055938-141055947
43	BCL11A	chr3:141055378-141056485	GM12878	blood:	n/a	chr3:141055938-141055947
44	BCL3	chr3:141050357-141051293	A549	lung:	n/a	chr3:141050755-141050764 chr3:141050848-141050861
45	BCL3	chr3:141050419-141050949	GM12878	blood:	n/a	chr3:141050755-141050764 chr3:141050848-141050861
46	BCL3	chr3:141030542-141031225	GM12878	blood:	n/a	n/a
47	BCL3	chr3:141030186-141030947	A549	lung:	n/a	n/a
48	BCL3	chr3:141050334-141051153	A549	lung:	n/a	chr3:141050755-141050764 chr3:141050848-141050861
49	BCL3	chr3:141055384-141056437	GM12878	blood:	n/a	chr3:141055938-141055947
50	BCL3	chr3:141029989-141031254	A549	lung:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:141032945-141032995	HepG2	liver:	n/a
2	chr3:141032945-141032995	HepG2	liver:	n/a
3	chr3:141030375-141030425	RPTEC	kidney:	n/a
4	chr3:141043080-141043130	HPAEpiC	pulmonary alveolar:	n/a
5	chr3:141043080-141043130	CMK	blood:	n/a
6	chr3:141042705-141042755	CMK	blood:	n/a
7	chr3:141032945-141032995	AoSMC	blood vessel:	n/a
8	chr3:141043080-141043130	AG09319	gingival:	n/a
9	chr3:141041770-141041820	U87	brain:	n/a
10	chr3:141041770-141041820	HIPEpiC	eye:	n/a
11	chr3:141042705-141042755	LNCaP	prostate:	n/a
12	chr3:141030609-141030659	Caco-2	colon:	n/a
13	chr3:141042988-141043038	AG09319	gingival:	n/a
14	chr3:141031715-141031765	BJ	skin:	n/a
15	chr3:141071669-141071719	K562	blood:	n/a
16	chr3:141030001-141030051	NH-A	brain:	n/a
17	chr3:141043480-141043530	GM12878	blood:	n/a
18	chr3:141030001-141030051	H1-hESC	embryonic stem cell:	embryo
19	chr3:141042705-141042755	IMR90	lung:	fetal
20	chr3:141041770-141041820	LNCaP	prostate:	n/a
21	chr3:141042988-141043038	HIPEpiC	eye:	n/a
22	chr3:141041959-141042009	HAEpiC	amniotic membrane:	n/a
23	chr3:141030001-141030051	NHDF-neo	bronchial:	n/a
24	chr3:141030588-141030638	AG04450	lung:	fetal
25	chr3:141043080-141043130	AG09309	skin:	n/a
26	chr3:141031715-141031765	SK-N-MC	brain:	n/a
27	chr3:141032945-141032995	GM12878	blood:	n/a
28	chr3:141030375-141030425	HCT-116	colon:	n/a
29	chr3:141030001-141030051	K562	blood:	n/a
30	chr3:141041959-141042009	HRCEpiC	kidney:	n/a
31	chr3:141042988-141043038	HCPEpiC	choroid plexus:	n/a
32	chr3:141071669-141071719	HEEpiC	esophagus:	n/a
33	chr3:141071669-141071719	HRCEpiC	kidney:	n/a
34	chr3:141030588-141030638	NHDF-neo	bronchial:	n/a
35	chr3:141041959-141042009	SK-N-SH	brain:	n/a
36	chr3:141071669-141071719	SK-N-MC	brain:	n/a
37	chr3:141041959-141042009	GM06990	blood:	n/a
38	chr3:141071669-141071719	T-47D	breast:	n/a
39	chr3:141043080-141043130	A549	lung:	n/a
40	chr3:141030761-141030811	ProgFib	skin:	n/a
41	chr3:141030588-141030638	SK-N-SH_RA	brain:	n/a
42	chr3:141041959-141042009	HPAEpiC	pulmonary alveolar:	n/a
43	chr3:141030761-141030811	GM06990	blood:	n/a
44	chr3:141030001-141030051	NT2-D1	testis:	n/a
45	chr3:141043080-141043130	HMEC	breast:	n/a
46	chr3:141030761-141030811	RPTEC	kidney:	n/a
47	chr3:141041959-141042009	PFSK-1	brain:	n/a
48	chr3:141041959-141042009	T-47D	breast:	n/a
49	chr3:141064812-141064862	HCT-116	colon:	n/a
50	chr3:141030001-141030051	Hepatocyte	liver:	n/a

(count:151 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:141030383..141031255-chr3:141170825..141171481,2	MCF-7	breast:
2	chr3:141041057..141042632-chr3:141043258..141046046,3	K562	blood:
3	chr3:141051493..141053638-chr3:141053830..141056565,2	K562	blood:
4	chr3:141030620..141031322-chr3:141079536..141080193,2	MCF-7	breast:
5	chr3:141047400..141052083-chr3:141058382..141063565,6	K562	blood:
6	chr3:141030651..141031191-chr3:141169108..141170020,2	MCF-7	breast:
7	chr3:141065346..141067226-chr3:141073466..141076149,2	K562	blood:
8	chr3:141070925..141073328-chr3:141073494..141076643,3	MCF-7	breast:
9	chr3:141043965..141046482-chr3:141049207..141051849,3	K562	blood:
10	chr2:44395356..44396337-chr3:141060035..141060554,2	Hela-S3	cervix:
11	chr3:141034875..141036826-chr3:141041844..141043916,3	MCF-7	breast:
12	chr3:141052445..141054291-chr3:141054574..141056796,2	MCF-7	breast:
13	chr3:141065346..141067226-chr3:141073466..141076149,2	K562	blood:
14	chr3:141061140..141064164-chr3:141067990..141071593,5	K562	blood:
15	chr3:140946906..140947764-chr3:141027081..141028157,3	MCF-7	breast:
16	chr3:141064419..141066966-chr3:141085745..141088370,3	K562	blood:
17	chr3:141038218..141041053-chr3:141044225..141046935,2	K562	blood:
18	chr3:141049236..141052063-chr3:141085767..141088852,6	K562	blood:
19	chr3:141022368..141022878-chr3:141030154..141030708,2	K562	blood:
20	chr3:141041057..141042632-chr3:141043258..141046046,3	K562	blood:
21	chr3:141030674..141032798-chr3:141168575..141172474,3	K562	blood:
22	chr3:141030231..141032200-chr3:141070469..141074049,3	K562	blood:
23	chr3:141050331..141052397-chr3:141073866..141075575,2	K562	blood:
24	chr3:141030343..141031265-chr3:141170565..141171975,8	K562	blood:
25	chr3:141052611..141055656-chr3:141065180..141068176,3	K562	blood:
26	chr3:141044721..141047194-chr3:141049083..141050797,2	MCF-7	breast:
27	chr3:141030424..141032274-chr3:141049079..141051494,2	MCF-7	breast:
28	chr3:141047658..141052071-chr3:141085661..141088836,5	K562	blood:
29	chr3:141031590..141033317-chr3:141034390..141037254,2	MCF-7	breast:
30	chr3:141069481..141071316-chr3:141086683..141088882,2	K562	blood:
31	chr3:141052611..141054382-chr3:141065464..141067942,2	K562	blood:
32	chr3:141028766..141032567-chr3:141157435..141160159,4	K562	blood:
33	chr3:141050917..141052882-chr3:141133782..141136338,2	K562	blood:
34	chr3:141047400..141052083-chr3:141058382..141063565,6	K562	blood:
35	chr3:141065959..141067603-chr3:141068508..141071378,2	MCF-7	breast:
36	chr3:141030270..141030782-chr3:141088625..141089300,2	K562	blood:
37	chr3:141071211..141074969-chr3:141075130..141079679,8	K562	blood:
38	chr3:141043965..141046482-chr3:141049207..141051849,3	K562	blood:
39	chr3:141061634..141065985-chr3:141070093..141073235,4	K562	blood:
40	chr3:140973529..140975169-chr3:141030843..141032626,2	K562	blood:
41	chr3:141062169..141064184-chr3:141073494..141075542,2	MCF-7	breast:
42	chr3:141068348..141070727-chr3:141071037..141073144,2	MCF-7	breast:
43	chr3:141030424..141032274-chr3:141049079..141051494,2	MCF-7	breast:
44	chr3:141074101..141082527-chr3:141083011..141090165,19	K562	blood:
45	chr3:141052611..141055656-chr3:141065180..141068176,3	K562	blood:
46	chr3:141069302..141073893-chr3:141077867..141081931,7	K562	blood:
47	chr3:140998151..140999834-chr3:141030561..141032150,2	K562	blood:
48	chr3:141057099..141059526-chr3:141069582..141072212,2	K562	blood:
49	chr3:141068348..141070727-chr3:141071037..141073144,2	MCF-7	breast:
50	chr3:141021371..141023874-chr3:141028085..141030183,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFDP2-11	chr3:141025328-141030534	NONHSAT092424
2	lnc-ACPL2-2	chr3:141053584-141054644	NONHSAT092426

No data

Variant related genes	Relation type
ENSG00000249540	TF binding region
ZBTB38	TF binding region
ENSG00000249540	CpG island
ZBTB38	CpG island
ENSG00000110200	chromatin interactions
ENSG00000249540	chromatin interactions
ENSG00000155893	chromatin interactions
ENSG00000156976	chromatin interactions
ENSG00000273106	chromatin interactions
ENSG00000177311	chromatin interactions
ENSG00000155903	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000249417	chromatin interactions
ENSG00000189403	chromatin interactions
ENSG00000138032	chromatin interactions

Extended variants
information (count: 1619 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:1619 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9968231	chr3:141027614-141027615	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs528265201	chr3:141027627-141027628	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
3	rs549554665	chr3:141027673-141027674	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
4	rs34853181	chr3:141027683-141027684	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
5	rs144231445	chr3:141027756-141027757	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
6	rs115861208	chr3:141027798-141027799	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
7	rs565190408	chr3:141027815-141027816	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
8	rs532563711	chr3:141027853-141027854	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
9	rs61224504	chr3:141027927-141027928	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
10	rs569220422	chr3:141027997-141027998	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
11	rs376101178	chr3:141027998-141027999	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs369081663	chr3:141028017-141028018	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
13	rs548896988	chr3:141028045-141028046	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
14	rs567109333	chr3:141028053-141028054	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
15	rs534347763	chr3:141028069-141028070	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
16	rs76614467	chr3:141028112-141028113	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
17	rs571226859	chr3:141028120-141028121	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
18	rs538641395	chr3:141028123-141028124	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs371301953	chr3:141028129-141028130	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs372370030	chr3:141028130-141028131	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs199860031	chr3:141028151-141028152	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs56998188	chr3:141028153-141028154	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs114134662	chr3:141028161-141028162	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs79132994	chr3:141028165-141028166	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs144645064	chr3:141028171-141028172	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs542559116	chr3:141028178-141028179	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs184236158	chr3:141028225-141028226	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs572707115	chr3:141028248-141028249	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
29	rs78188647	chr3:141028316-141028317	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs78169668	chr3:141028319-141028320	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs34113266	chr3:141028328-141028329	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
32	rs187106727	chr3:141028352-141028353	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
33	rs148082122	chr3:141028359-141028360	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
34	rs35889786	chr3:141028496-141028497	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
35	rs544672582	chr3:141028501-141028502	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
36	rs189838949	chr3:141028508-141028509	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
37	rs141853699	chr3:141028564-141028565	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
38	rs548907042	chr3:141028582-141028583	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
39	rs182081562	chr3:141028599-141028600	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
40	rs150633309	chr3:141028633-141028634	Weak transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
41	rs112397079	chr3:141028716-141028717	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
42	rs373833407	chr3:141028753-141028754	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
43	rs33999335	chr3:141028774-141028775	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
44	rs397877663	chr3:141028788-141028789	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
45	rs369519035	chr3:141028797-141028798	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
46	rs543285939	chr3:141028808-141028809	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
47	rs376800933	chr3:141028837-141028838	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
48	rs550645797	chr3:141028838-141028839	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
49	rs568551387	chr3:141028861-141028862	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
50	rs556793483	chr3:141028888-141028889	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

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
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
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
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
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1255 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141012000-141029800	Weak transcription	Right Ventricle	heart
2	chr3:141012200-141029800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr3:141012200-141029800	Weak transcription	Brain Germinal Matrix	brain
4	chr3:141012200-141029800	Weak transcription	Left Ventricle	heart
5	chr3:141014000-141029800	Weak transcription	Spleen	Spleen
6	chr3:141014000-141030000	Weak transcription	Aorta	Aorta
7	chr3:141014200-141029800	Weak transcription	Right Atrium	heart
8	chr3:141021800-141029800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr3:141021800-141029800	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr3:141022600-141029400	Weak transcription	Hela-S3	cervix
11	chr3:141022600-141029800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr3:141022800-141029600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr3:141022800-141030000	Weak transcription	HSMMtube	muscle
14	chr3:141023000-141029400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr3:141023000-141029600	Weak transcription	Adipose Nuclei	Adipose
16	chr3:141023000-141029800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr3:141023000-141029800	Weak transcription	Brain Hippocampus Middle	brain
18	chr3:141023000-141029800	Weak transcription	Brain Substantia Nigra	brain
19	chr3:141023000-141029800	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr3:141023000-141030000	Weak transcription	Esophagus	oesophagus
21	chr3:141023200-141029800	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr3:141023200-141029800	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr3:141023200-141029800	Weak transcription	Osteobl	bone
24	chr3:141023400-141029800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr3:141023600-141029600	Weak transcription	Fetal Heart	heart
26	chr3:141024000-141029600	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr3:141024400-141029400	Weak transcription	A549	lung
28	chr3:141024800-141029800	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr3:141025800-141029800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr3:141025800-141029800	Weak transcription	NHDF-Ad	bronchial
31	chr3:141026000-141029600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr3:141026000-141029800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr3:141026000-141029800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr3:141026000-141029800	Weak transcription	NHLF	lung
35	chr3:141026400-141029200	Weak transcription	GM12878-XiMat	blood
36	chr3:141026400-141029800	Enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr3:141026400-141029800	Weak transcription	Fetal Intestine Small	intestine
38	chr3:141026600-141027800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr3:141026600-141027800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr3:141026600-141028400	Enhancers	Primary T cells fromperipheralblood	blood
41	chr3:141026800-141028000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr3:141026800-141028000	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr3:141026800-141028000	Enhancers	Fetal Intestine Large	intestine
44	chr3:141026800-141029600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr3:141026800-141029600	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr3:141027000-141027800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr3:141027000-141028000	Enhancers	Primary T cells from cord blood	blood
48	chr3:141027000-141029400	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr3:141027200-141027800	Enhancers	Pancreas	Pancrea
50	chr3:141027200-141027800	Enhancers	Sigmoid Colon	Sigmoid Colon

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