Variant report

Variant	nsv872179
Chromosome Location	chr1:120131597-120162787
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:711)
CpG islands
(count:122)
Chromatin interactive
region (count:32)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:711 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:120156546-120156764	HepG2	liver:	n/a	n/a
2	ATF1	chr1:120151890-120151896	K562	blood:	n/a	n/a
3	ATF1	chr1:120157910-120157934	K562	blood:	n/a	n/a
4	ATF3	chr1:120154276-120154532	K562	blood:	n/a	n/a
5	ATF3	chr1:120154165-120154614	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr1:120156447-120156806	K562	blood:	n/a	n/a
7	BHLHE40	chr1:120156581-120156796	A549	lung:	n/a	n/a
8	BHLHE40	chr1:120156467-120156621	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:120154235-120154668	K562	blood:	n/a	n/a
10	BRCA1	chr1:120156588-120156779	HepG2	liver:	n/a	n/a
11	BRCA1	chr1:120156426-120156738	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr1:120152140-120152301	H1-hESC	embryonic stem cell:	n/a	chr1:120152213-120152224
13	CEBPB	chr1:120144744-120145076	A549	lung:	n/a	chr1:120144889-120144900
14	CEBPB	chr1:120152171-120152183	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:120144888-120144965	H1-hESC	embryonic stem cell:	n/a	chr1:120144889-120144900
16	CEBPB	chr1:120144741-120145077	HepG2	liver:	n/a	chr1:120144889-120144900
17	CEBPB	chr1:120144827-120145081	Hela-S3	cervix:	n/a	chr1:120144889-120144900
18	CEBPB	chr1:120154268-120154461	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:120152150-120152238	K562	blood:	n/a	chr1:120152213-120152224
20	CEBPB	chr1:120142586-120142702	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr1:120156604-120156671	GM12878	blood:	n/a	n/a
22	CHD2	chr1:120156617-120156737	K562	blood:	n/a	n/a
23	CHD2	chr1:120154302-120154481	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr1:120154059-120154552	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr1:120156558-120156728	GM12878	blood:	n/a	n/a
26	CTCF	chr1:120150122-120150361	ProgFib	skin:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
27	CTCF	chr1:120156400-120156550	HAc	cerebellar:	n/a	n/a
28	CTCF	chr1:120156417-120156717	GM19238	blood:	n/a	chr1:120156563-120156584 chr1:120156564-120156577 chr1:120156562-120156578
29	CTCF	chr1:120156540-120156690	GM12865	blood:	n/a	chr1:120156563-120156584 chr1:120156564-120156577 chr1:120156562-120156578
30	CTCF	chr1:120156540-120156690	HAc	cerebellar:	n/a	chr1:120156563-120156584 chr1:120156564-120156577 chr1:120156562-120156578
31	CTCF	chr1:120154276-120154532	MCF-7	breast:	n/a	chr1:120154411-120154432
32	CTCF	chr1:120156460-120156610	HFF-Myc	foreskin:	n/a	chr1:120156563-120156584 chr1:120156564-120156577 chr1:120156562-120156578
33	CTCF	chr1:120154269-120154531	Spleen_OC	spleen:	n/a	chr1:120154411-120154432
34	CTCF	chr1:120156460-120156736	SK-N-SH_RA	brain:	n/a	chr1:120156563-120156584 chr1:120156564-120156577 chr1:120156562-120156578
35	CTCF	chr1:120156381-120156729	A549	lung:	n/a	chr1:120156563-120156584 chr1:120156564-120156577 chr1:120156562-120156578
36	CTCF	chr1:120154340-120154490	GM12870	blood:	n/a	chr1:120154411-120154432
37	CTCF	chr1:120156431-120156727	LNCaP	prostate:	n/a	chr1:120156563-120156584 chr1:120156564-120156577 chr1:120156562-120156578
38	CTCF	chr1:120156540-120156690	HBMEC	blood vessel:	n/a	chr1:120156563-120156584 chr1:120156564-120156577 chr1:120156562-120156578
39	CTCF	chr1:120156120-120156270	GM12871	blood:	n/a	n/a
40	CTCF	chr1:120150060-120150210	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr1:120154320-120154470	HVMF	connective:	n/a	chr1:120154411-120154432
42	CTCF	chr1:120154340-120154490	RPTEC	kidney:	n/a	chr1:120154411-120154432
43	CTCF	chr1:120156540-120156690	HUVEC	blood vessel:	n/a	chr1:120156563-120156584 chr1:120156564-120156577 chr1:120156562-120156578
44	CTCF	chr1:120154300-120154450	AG04450	lung:	n/a	chr1:120154411-120154432
45	CTCF	chr1:120154270-120154543	Pancreas_OC	pancreas:	n/a	chr1:120154411-120154432
46	CTCF	chr1:120150134-120150401	LNCaP	prostate:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
47	CTCF	chr1:120156500-120156650	BE2_C	brain:	n/a	chr1:120156563-120156584 chr1:120156564-120156577 chr1:120156562-120156578
48	CTCF	chr1:120156364-120156795	K562	blood:	n/a	chr1:120156563-120156584 chr1:120156564-120156577 chr1:120156562-120156578
49	CTCF	chr1:120149960-120150110	GM12872	blood:	n/a	n/a
50	CTCF	chr1:120154320-120154470	GM06990	blood:	n/a	chr1:120154411-120154432

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120156779-120156829	HCM	heart:	n/a
2	chr1:120143242-120143292	T-47D	breast:	n/a
3	chr1:120156779-120156829	HEEpiC	esophagus:	n/a
4	chr1:120143242-120143292	HPAEpiC	pulmonary alveolar:	n/a
5	chr1:120156779-120156829	BE2_C	brain:	n/a
6	chr1:120143242-120143292	NHBE	bronchial:	n/a
7	chr1:120143242-120143292	HIPEpiC	eye:	n/a
8	chr1:120156779-120156829	GM12892	blood:	n/a
9	chr1:120143242-120143292	AG10803	skin:	n/a
10	chr1:120156779-120156829	HIPEpiC	eye:	n/a
11	chr1:120143242-120143292	HAEpiC	amniotic membrane:	n/a
12	chr1:120143242-120143292	NHDF-neo	bronchial:	n/a
13	chr1:120143242-120143292	HCF	heart:	n/a
14	chr1:120156779-120156829	Hela-S3	cervix:	n/a
15	chr1:120143242-120143292	HEEpiC	esophagus:	n/a
16	chr1:120143242-120143292	SK-N-MC	brain:	n/a
17	chr1:120156779-120156829	NT2-D1	testis:	n/a
18	chr1:120156779-120156829	HRE	kidney:	n/a
19	chr1:120143242-120143292	BE2_C	brain:	n/a
20	chr1:120156779-120156829	SAEC	small airway:	n/a
21	chr1:120156779-120156829	SK-N-SH_RA	brain:	n/a
22	chr1:120156779-120156829	ProgFib	skin:	n/a
23	chr1:120143242-120143292	SKMC	muscle:	n/a
24	chr1:120156779-120156829	HepG2	liver:	n/a
25	chr1:120143242-120143292	NH-A	brain:	n/a
26	chr1:120156779-120156829	CMK	blood:	n/a
27	chr1:120143242-120143292	AG09309	skin:	n/a
28	chr1:120143242-120143292	HCM	heart:	n/a
29	chr1:120156779-120156829	NB4	blood:	n/a
30	chr1:120156779-120156829	SKMC	muscle:	n/a
31	chr1:120156779-120156829	SK-N-MC	brain:	n/a
32	chr1:120143242-120143292	HepG2	liver:	n/a
33	chr1:120156779-120156829	MCF-7	breast:	n/a
34	chr1:120143242-120143292	PFSK-1	brain:	n/a
35	chr1:120156779-120156829	GM06990	blood:	n/a
36	chr1:120143242-120143292	GM12891	blood:	n/a
37	chr1:120156779-120156829	BJ	skin:	n/a
38	chr1:120143242-120143292	AG04449	skin:	fetal
39	chr1:120143242-120143292	ECC-1	luminal epithelium:	n/a
40	chr1:120156779-120156829	HAEpiC	amniotic membrane:	n/a
41	chr1:120143242-120143292	Caco-2	colon:	n/a
42	chr1:120156779-120156829	Caco-2	colon:	n/a
43	chr1:120156779-120156829	HL-60	blood:	n/a
44	chr1:120156779-120156829	AoSMC	blood vessel:	n/a
45	chr1:120156779-120156829	A549	lung:	n/a
46	chr1:120156779-120156829	HUVEC	blood vessel:	n/a
47	chr1:120156779-120156829	HMEC	breast:	n/a
48	chr1:120156779-120156829	LNCaP	prostate:	n/a
49	chr1:120143242-120143292	HRPEpiC	eye:	n/a
50	chr1:120143242-120143292	HCPEpiC	choroid plexus:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:120091982..120092950-chr1:120156090..120157044,3	MCF-7	breast:
2	chr1:120156759..120158613-chr1:120204611..120207456,2	MCF-7	breast:
3	chr1:120154194..120154867-chr1:120205886..120206437,3	MCF-7	breast:
4	chr1:120156408..120157049-chr1:120218285..120218819,2	MCF-7	breast:
5	chr1:120091982..120092921-chr1:120150180..120150935,3	MCF-7	breast:
6	chr1:120158069..120159004-chr1:120217770..120218396,2	K562	blood:
7	chr1:120125219..120126121-chr1:120153919..120154547,2	MCF-7	breast:
8	chr1:119914912..119915700-chr1:120154301..120154847,3	MCF-7	breast:
9	chr1:120153476..120155640-chr1:120190161..120192811,2	K562	blood:
10	chr1:120145059..120147660-chr1:120162749..120165475,2	MCF-7	breast:
11	chr1:120151431..120154337-chr1:120190081..120192940,2	MCF-7	breast:
12	chr1:120153709..120155634-chr1:120202418..120204087,2	MCF-7	breast:
13	chr1:120154731..120156704-chr1:120158612..120160451,2	MCF-7	breast:
14	chr1:120156126..120157196-chr1:120217116..120218704,11	MCF-7	breast:
15	chr1:120162586..120166440-chr1:120167182..120171199,5	K562	blood:
16	chr1:120159569..120162052-chr1:120189415..120191074,2	MCF-7	breast:
17	chr1:120156154..120156980-chr1:120205229..120206054,4	MCF-7	breast:
18	chr1:120160558..120163551-chr1:120189552..120191710,2	MCF-7	breast:
19	chr1:120156097..120157073-chr1:120205512..120206469,8	MCF-7	breast:
20	chr1:120154003..120154965-chr1:120217033..120218809,10	K562	blood:
21	chr1:120161786..120164966-chr1:120184691..120189749,4	K562	blood:
22	chr1:120154324..120155309-chr1:120205532..120206464,6	MCF-7	breast:
23	chr1:120154024..120154620-chr1:120217678..120218364,2	MCF-7	breast:
24	chr1:120154067..120155007-chr1:120217498..120218673,7	MCF-7	breast:
25	chr1:120162086..120165079-chr1:120173514..120175556,2	MCF-7	breast:
26	chr1:120156082..120157034-chr1:120205464..120206953,8	K562	blood:
27	chr1:120155133..120157085-chr1:120217009..120218744,10	K562	blood:
28	chr1:120154731..120156704-chr1:120158612..120160451,2	MCF-7	breast:
29	chr1:120145059..120147660-chr1:120162749..120165475,2	MCF-7	breast:
30	chr1:120161786..120164966-chr1:120187188..120189749,3	K562	blood:
31	chr1:120156150..120157072-chr1:120189041..120189869,2	MCF-7	breast:
32	chr1:120161780..120163387-chr1:120165272..120166902,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF697-1	chr1:120140325-120141914	NONHSAT005570
2	lnc-ZNF697-2	chr1:120162038-120164121	NONHSAT005572
3	lnc-ZNF697-3	chr1:120148999-120149695	NONHSAT005569
4	lnc-ZNF697-1	chr1:120140325-120141894	ENSG00000260941.1
5	lnc-PHGDH-1	chr1:120144910-120145118	ENSG00000242959.1
6	lnc-PHGDH-1	chr1:120143780-120144107	ENSG00000242959.1

No data

Variant related genes	Relation type
LINC00622	TF binding region
GAPDHP33	TF binding region
HSD3BP5	TF binding region
LINC00622	CpG island
GAPDHP33	CpG island
HSD3BP5	CpG island
ENSG00000143067	chromatin interactions
ENSG00000092621	chromatin interactions

Extended variants
information (count: 1349 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1349 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12139088	chr1:120131597-120131598	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587651986	chr1:120131634-120131635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149186782	chr1:120131661-120131662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs142577098	chr1:120131671-120131672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs346678	chr1:120131751-120131752	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs184160930	chr1:120131753-120131754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs74114711	chr1:120131772-120131773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376923326	chr1:120131779-120131780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs587636746	chr1:120131784-120131785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs587694039	chr1:120131797-120131798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs587753522	chr1:120131814-120131815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587716384	chr1:120131866-120131867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138508865	chr1:120131869-120131870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs587649290	chr1:120131873-120131874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587712702	chr1:120131910-120131911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs587607075	chr1:120131952-120131953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs587642232	chr1:120131966-120131967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200489808	chr1:120131967-120131968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150962901	chr1:120131982-120131983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs140866419	chr1:120131986-120131987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185058010	chr1:120132036-120132037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs587762398	chr1:120132082-120132083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144609042	chr1:120132147-120132148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs587667839	chr1:120132155-120132156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs587731323	chr1:120132222-120132223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587616971	chr1:120132226-120132227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112350215	chr1:120132228-120132229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs587681987	chr1:120132299-120132300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs587740841	chr1:120132315-120132316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs346679	chr1:120132331-120132332	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs587702095	chr1:120132337-120132338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs346680	chr1:120132346-120132347	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs140454112	chr1:120132473-120132474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs587687107	chr1:120132480-120132481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs346681	chr1:120132493-120132494	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs587635180	chr1:120132520-120132521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs201315776	chr1:120132612-120132613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs587617480	chr1:120132624-120132625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs587658265	chr1:120132692-120132693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs587739804	chr1:120132707-120132708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs201763258	chr1:120132727-120132728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200009280	chr1:120132728-120132729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs201281115	chr1:120132729-120132730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182385967	chr1:120132772-120132773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs370489262	chr1:120132803-120132804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs149504488	chr1:120132862-120132863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142737701	chr1:120132880-120132881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11808154	chr1:120132916-120132917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs587605761	chr1:120132925-120132926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs587653462	chr1:120132939-120132940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Aetanephric adenomas	20802469	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Systemic lupus erythematosus	21956041	CNVD
Breast cancer	21804112	CNVD
Mental retardation	21062444	CNVD
Myelofibrosis	22110671	CNVD
Emphysema	19352772	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Cancer	21272361	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120115200-120160800	Weak transcription	Gastric	stomach
2	chr1:120129000-120132600	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr1:120129000-120132800	Weak transcription	Fetal Intestine Small	intestine
4	chr1:120129200-120133200	Weak transcription	Adipose Nuclei	Adipose
5	chr1:120129600-120132200	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr1:120130000-120131600	Enhancers	Fetal Lung	lung
7	chr1:120130200-120138800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:120130200-120139000	Weak transcription	Left Ventricle	heart
9	chr1:120130400-120133200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:120130600-120136400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:120131000-120132200	Weak transcription	Fetal Intestine Large	intestine
12	chr1:120131000-120133200	Weak transcription	Placenta	Placenta
13	chr1:120132200-120133000	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr1:120132200-120134800	Enhancers	Fetal Intestine Large	intestine
15	chr1:120132600-120134000	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr1:120132800-120135000	Enhancers	Fetal Intestine Small	intestine
17	chr1:120133000-120133800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr1:120133200-120133600	Enhancers	Adipose Nuclei	Adipose
19	chr1:120133200-120133600	Enhancers	Placenta	Placenta
20	chr1:120133200-120134400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:120133400-120134400	Enhancers	Pancreas	Pancrea
22	chr1:120133600-120144800	Weak transcription	Placenta	Placenta
23	chr1:120133800-120134400	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr1:120134400-120136200	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr1:120135000-120136400	Weak transcription	Fetal Intestine Small	intestine
26	chr1:120135200-120151000	Weak transcription	Fetal Stomach	stomach
27	chr1:120136200-120137000	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr1:120136400-120136800	ZNF genes & repeats	Fetal Intestine Small	intestine
29	chr1:120136400-120139200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr1:120136400-120139600	Enhancers	HMEC	breast
31	chr1:120136600-120137000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:120136800-120137200	Enhancers	NHEK	skin
33	chr1:120136800-120139200	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr1:120136800-120142800	Weak transcription	Fetal Intestine Small	intestine
35	chr1:120137000-120137600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr1:120137200-120137600	Weak transcription	NHEK	skin
37	chr1:120137200-120139400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr1:120137600-120139000	Enhancers	NHEK	skin
39	chr1:120137800-120138400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:120137800-120138400	Enhancers	Brain Hippocampus Middle	brain
41	chr1:120137800-120138800	Enhancers	Brain Cingulate Gyrus	brain
42	chr1:120138000-120138200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
43	chr1:120138000-120138400	Enhancers	Brain Angular Gyrus	brain
44	chr1:120138000-120138800	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr1:120138200-120138800	Enhancers	Brain Anterior Caudate	brain
46	chr1:120138200-120139400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr1:120138400-120139000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr1:120138400-120139000	Enhancers	HUVEC	blood vessel
49	chr1:120138400-120140600	Weak transcription	Brain Angular Gyrus	brain
50	chr1:120138800-120139000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived

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