Variant report

Variant	nsv872583
Chromosome Location	chr1:183955574-184015663
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1115)
CpG islands
(count:1344)
Chromatin interactive
region (count:82)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1115 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:183957742-183957900	K562	blood:	n/a	n/a
2	ARID3A	chr1:183971371-183971801	K562	blood:	n/a	n/a
3	ARID3A	chr1:184004352-184005170	K562	blood:	n/a	n/a
4	ARID3A	chr1:184001503-184001984	K562	blood:	n/a	n/a
5	ARID3A	chr1:183955919-183955978	K562	blood:	n/a	n/a
6	ARID3A	chr1:183956621-183957492	K562	blood:	n/a	n/a
7	ARID3A	chr1:183958111-183958609	K562	blood:	n/a	n/a
8	ARID3A	chr1:183971363-183971604	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:183994355-183994614	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:183962322-183962735	HepG2	liver:	n/a	n/a
11	ARID3A	chr1:183962152-183962728	K562	blood:	n/a	n/a
12	ARID3A	chr1:183993804-183994356	K562	blood:	n/a	n/a
13	ARID3A	chr1:183967005-183967909	K562	blood:	n/a	n/a
14	ARID3A	chr1:183965060-183965483	K562	blood:	n/a	n/a
15	ARID3A	chr1:183998318-183998767	K562	blood:	n/a	n/a
16	ARID3A	chr1:184002236-184002945	K562	blood:	n/a	n/a
17	ARID3A	chr1:183999711-184001097	K562	blood:	n/a	n/a
18	ATF1	chr1:183966994-183967440	K562	blood:	n/a	n/a
19	ATF1	chr1:183980811-183980885	K562	blood:	n/a	n/a
20	ATF1	chr1:183961099-183961925	K562	blood:	n/a	n/a
21	ATF1	chr1:183999569-183999986	K562	blood:	n/a	n/a
22	ATF1	chr1:183958227-183958682	K562	blood:	n/a	n/a
23	ATF1	chr1:183965583-183965918	K562	blood:	n/a	n/a
24	ATF1	chr1:183962210-183962682	K562	blood:	n/a	n/a
25	ATF1	chr1:183993826-183994242	K562	blood:	n/a	n/a
26	ATF1	chr1:184002787-184003252	K562	blood:	n/a	n/a
27	ATF1	chr1:184001475-184001621	K562	blood:	n/a	n/a
28	ATF1	chr1:184006761-184007125	K562	blood:	n/a	n/a
29	ATF1	chr1:184002230-184002580	K562	blood:	n/a	n/a
30	ATF1	chr1:184000325-184001006	K562	blood:	n/a	n/a
31	ATF1	chr1:183956804-183957043	K562	blood:	n/a	n/a
32	ATF2	chr1:183958029-183958808	GM12878	blood:	n/a	n/a
33	ATF2	chr1:183958147-183958715	GM12878	blood:	n/a	n/a
34	ATF3	chr1:184002176-184002573	K562	blood:	n/a	n/a
35	ATF3	chr1:183965646-183965840	K562	blood:	n/a	n/a
36	ATF3	chr1:184006796-184007231	K562	blood:	n/a	n/a
37	ATF3	chr1:184000281-184000946	K562	blood:	n/a	n/a
38	BACH1	chr1:183971280-183971862	H1-hESC	embryonic stem cell:	n/a	chr1:183971486-183971500
39	BACH1	chr1:183971217-183971645	K562	blood:	n/a	chr1:183971486-183971500
40	BACH1	chr1:183998449-183998572	K562	blood:	n/a	n/a
41	BATF	chr1:183958226-183958546	GM12878	blood:	n/a	n/a
42	BATF	chr1:183958239-183958672	GM12878	blood:	n/a	n/a
43	BCL11A	chr1:183958258-183958598	GM12878	blood:	n/a	chr1:183958364-183958373
44	BCL11A	chr1:183958123-183958684	GM12878	blood:	n/a	chr1:183958364-183958373
45	BCL3	chr1:183958140-183958695	GM12878	blood:	n/a	chr1:183958364-183958373
46	BCLAF1	chr1:183958141-183958662	GM12878	blood:	n/a	chr1:183958364-183958373
47	BCLAF1	chr1:183958162-183958671	GM12878	blood:	n/a	chr1:183958364-183958373
48	BCLAF1	chr1:184000133-184000983	K562	blood:	n/a	n/a
49	BHLHE40	chr1:183958240-183958699	K562	blood:	n/a	n/a
50	BHLHE40	chr1:183991048-183991060	K562	blood:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:184006496-184006546	BJ	skin:	n/a
2	chr1:184005360-184005410	HMEC	breast:	n/a
3	chr1:184006496-184006546	BJ	skin:	n/a
4	chr1:184005360-184005410	HMEC	breast:	n/a
5	chr1:184005360-184005410	PrEC	prostate:	n/a
6	chr1:184006496-184006546	HL-60	blood:	n/a
7	chr1:184005063-184005113	HCT-116	colon:	n/a
8	chr1:184007803-184007853	SK-N-SH_RA	brain:	n/a
9	chr1:184007803-184007853	NHDF-neo	bronchial:	n/a
10	chr1:184006496-184006546	SKMC	muscle:	n/a
11	chr1:184006496-184006546	HCT-116	colon:	n/a
12	chr1:183971636-183971686	MCF-7	breast:	n/a
13	chr1:183971636-183971686	A549	lung:	n/a
14	chr1:184005990-184006040	Hela-S3	cervix:	n/a
15	chr1:184006816-184006866	HCT-116	colon:	n/a
16	chr1:184005360-184005410	NHDF-neo	bronchial:	n/a
17	chr1:183971636-183971686	NH-A	brain:	n/a
18	chr1:183957982-183958032	GM12878	blood:	n/a
19	chr1:184005063-184005113	AG09319	gingival:	n/a
20	chr1:184005534-184005584	NHDF-neo	bronchial:	n/a
21	chr1:184007101-184007151	H1-hESC	embryonic stem cell:	embryo
22	chr1:184006765-184006815	HNPCEpiC	eye:	n/a
23	chr1:184009497-184009547	U87	brain:	n/a
24	chr1:184006285-184006335	HRE	kidney:	n/a
25	chr1:184009497-184009547	PFSK-1	brain:	n/a
26	chr1:184006765-184006815	Hela-S3	cervix:	n/a
27	chr1:184006285-184006335	AG04450	lung:	fetal
28	chr1:184005534-184005584	HRCEpiC	kidney:	n/a
29	chr1:184006765-184006815	ProgFib	skin:	n/a
30	chr1:184009497-184009547	GM12892	blood:	n/a
31	chr1:184005896-184005946	Hepatocyte	liver:	n/a
32	chr1:184008235-184008285	SAEC	small airway:	n/a
33	chr1:184006285-184006335	Hela-S3	cervix:	n/a
34	chr1:184006216-184006266	RPTEC	kidney:	n/a
35	chr1:184007101-184007151	K562	blood:	n/a
36	chr1:184009497-184009547	SK-N-SH	brain:	n/a
37	chr1:183971636-183971686	U87	brain:	n/a
38	chr1:184006816-184006866	HNPCEpiC	eye:	n/a
39	chr1:183957982-183958032	NB4	blood:	n/a
40	chr1:184006933-184006983	PrEC	prostate:	n/a
41	chr1:184006765-184006815	HEEpiC	esophagus:	n/a
42	chr1:184009497-184009547	SK-N-MC	brain:	n/a
43	chr1:184005360-184005410	HCM	heart:	n/a
44	chr1:183965312-183965362	HUVEC	blood vessel:	n/a
45	chr1:184006216-184006266	LNCaP	prostate:	n/a
46	chr1:184008235-184008285	Hepatocyte	liver:	n/a
47	chr1:184007101-184007151	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:184005360-184005410	GM06990	blood:	n/a
49	chr1:184008235-184008285	A549	lung:	n/a
50	chr1:184006496-184006546	H1-hESC	embryonic stem cell:	embryo

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:183943940..183946448-chr1:183997966..184000814,2	K562	blood:
2	chr1:183960151..183962880-chr14:24605342..24606992,2	MCF-7	breast:
3	chr1:183958400..183961976-chr1:183962381..183964595,3	MCF-7	breast:
4	chr1:184012895..184017292-chr1:184018283..184022966,11	MCF-7	breast:
5	chr1:183966449..183970742-chr1:183981274..183983933,4	K562	blood:
6	chr1:183978007..183980977-chr1:183981076..183984748,5	K562	blood:
7	chr1:183971472..183974918-chr1:183978540..183982820,5	K562	blood:
8	chr1:182807885..182810341-chr1:184000416..184002288,2	K562	blood:
9	chr1:183955994..183963438-chr1:184018687..184025701,10	K562	blood:
10	chr1:183890561..183893441-chr1:183998766..184002920,3	K562	blood:
11	chr1:183948339..183950247-chr1:183954738..183957083,2	K562	blood:
12	chr1:183975497..183978349-chr1:183979373..183981183,2	MCF-7	breast:
13	chr1:183958400..183961976-chr1:183962381..183964595,3	MCF-7	breast:
14	chr1:183978007..183979662-chr1:183981076..183984344,3	K562	blood:
15	chr1:183960708..183962804-chr1:183986708..183988733,2	K562	blood:
16	chr1:183887976..183889983-chr1:184001023..184003868,2	K562	blood:
17	chr1:183966025..183968649-chr1:183970110..183972411,2	MCF-7	breast:
18	chr1:183961368..183963694-chr1:183965617..183967704,2	MCF-7	breast:
19	chr1:183968128..183970872-chr1:183981037..183985172,5	K562	blood:
20	chr1:183967387..183970821-chr1:183971307..183974997,4	K562	blood:
21	chr1:184001838..184006265-chr1:184019674..184022960,4	MCF-7	breast:
22	chr1:183961286..183963982-chr1:183968217..183971104,2	K562	blood:
23	chr1:184004028..184006606-chr1:184019483..184022973,3	MCF-7	breast:
24	chr1:183938366..183941227-chr1:183976476..183978460,2	K562	blood:
25	chr1:183603690..183605238-chr1:184005001..184007460,2	K562	blood:
26	chr1:184004909..184006450-chr1:184057405..184059621,2	K562	blood:
27	chr1:183971721..183974918-chr1:183978540..183981272,3	K562	blood:
28	chr1:183900176..183902454-chr1:184003070..184005621,2	K562	blood:
29	chr1:183907178..183909194-chr1:183997885..184000695,2	K562	blood:
30	chr1:183966449..183970742-chr1:183981274..183983933,4	K562	blood:
31	chr1:183884586..183886090-chr1:184008037..184009879,2	K562	blood:
32	chr1:183996561..183999436-chr1:184003506..184005504,2	MCF-7	breast:
33	chr1:184002927..184005437-chr1:184006941..184009793,2	MCF-7	breast:
34	chr1:183971472..183974918-chr1:183978540..183982820,5	K562	blood:
35	chr1:183961368..183963694-chr1:183965617..183967704,2	MCF-7	breast:
36	chr1:183954395..183958643-chr1:183998431..184003306,4	K562	blood:
37	chr1:183993100..183996094-chr1:184020312..184022117,2	MCF-7	breast:
38	chr1:183958819..183961502-chr1:183969906..183972201,2	K562	blood:
39	chr1:183921738..183924385-chr1:183994852..183996803,2	K562	blood:
40	chr1:183950977..183955895-chr1:183999343..184002420,4	K562	blood:
41	chr1:183961286..183963982-chr1:183968217..183971104,2	K562	blood:
42	chr1:183902079..183905067-chr1:183998607..184000685,2	K562	blood:
43	chr1:183964839..183967146-chr1:183970545..183972322,3	K562	blood:
44	chr1:183947733..183950013-chr1:183997386..184000802,4	K562	blood:
45	chr1:183958599..183960225-chr1:183979032..183981133,2	K562	blood:
46	chr1:183951094..183952829-chr1:183954460..183956370,2	K562	blood:
47	chr1:183968067..183969745-chr1:183975165..183977990,2	K562	blood:
48	chr1:183952222..183954901-chr1:183961001..183962966,2	K562	blood:
49	chr1:183901365..183904331-chr1:184007121..184010101,2	K562	blood:
50	chr1:183960708..183962804-chr1:183986708..183988733,2	K562	blood:

No data

Variant related genes	Relation type
COLGALT2	TF binding region
COLGALT2	CpG island
ENSG00000135829	chromatin interactions
ENSG00000198860	chromatin interactions
ENSG00000198756	chromatin interactions
ENSG00000233223	chromatin interactions
ENSG00000143344	chromatin interactions
ENSG00000129255	chromatin interactions
ENSG00000162704	chromatin interactions
ENSG00000092010	chromatin interactions

Extended variants
information (count: 2168 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2168 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1926868	chr1:183955574-183955575	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564657935	chr1:183955575-183955576	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs187243158	chr1:183955620-183955621	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs550204798	chr1:183955622-183955623	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs142510931	chr1:183955679-183955680	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs540130180	chr1:183955706-183955707	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs1926867	chr1:183955742-183955743	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs146872877	chr1:183955770-183955771	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs1926866	chr1:183955791-183955792	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs144806088	chr1:183955804-183955805	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs559173536	chr1:183955805-183955806	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs114436550	chr1:183955852-183955853	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs538332430	chr1:183955862-183955863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534096516	chr1:183955903-183955904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs74130497	chr1:183955911-183955912	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs191601596	chr1:183955917-183955918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542164264	chr1:183955920-183955921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554580201	chr1:183956009-183956010	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs573061042	chr1:183956074-183956075	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs540074631	chr1:183956078-183956079	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs59990920	chr1:183956184-183956185	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs376476302	chr1:183956190-183956191	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs574425436	chr1:183956206-183956207	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs147598913	chr1:183956213-183956214	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs543907417	chr1:183956262-183956263	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs183170095	chr1:183956275-183956276	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188055628	chr1:183956279-183956280	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs10797928	chr1:183956344-183956345	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs192963066	chr1:183956350-183956351	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs527970378	chr1:183956362-183956363	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs552844155	chr1:183956363-183956364	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs571053173	chr1:183956398-183956399	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs6696539	chr1:183956410-183956411	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs556701937	chr1:183956441-183956442	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs568504917	chr1:183956447-183956448	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs142058420	chr1:183956451-183956452	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs150087965	chr1:183956460-183956461	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs375056290	chr1:183956481-183956482	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs183762422	chr1:183956482-183956483	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs371965609	chr1:183956504-183956505	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs186940432	chr1:183956509-183956510	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs576638492	chr1:183956522-183956523	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs138359393	chr1:183956593-183956594	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs562467795	chr1:183956616-183956617	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs148907011	chr1:183956633-183956634	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs143588360	chr1:183956639-183956640	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs192376221	chr1:183956665-183956666	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs34373454	chr1:183956688-183956689	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs80263077	chr1:183956732-183956733	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs2182624	chr1:183956758-183956759	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Renal cell carcinoma	18765545	CNVD
Nephroblastoma	17189400	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD

Chromatin state (count:1362 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:183902600-183965200	Weak transcription	Left Ventricle	heart
2	chr1:183923200-183961000	Weak transcription	Pancreas	Pancrea
3	chr1:183952000-183958800	Enhancers	NHDF-Ad	bronchial
4	chr1:183953000-183959000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr1:183953000-183965200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:183953200-183957400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:183953600-183957600	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr1:183953800-183956600	Weak transcription	Brain Anterior Caudate	brain
9	chr1:183953800-183965200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr1:183954000-183956000	Weak transcription	Fetal Heart	heart
11	chr1:183954000-183956400	Weak transcription	Brain Angular Gyrus	brain
12	chr1:183954000-183958400	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr1:183954000-183965600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr1:183954200-183956000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr1:183954200-183956000	Weak transcription	Brain Cingulate Gyrus	brain
16	chr1:183954200-183956000	Weak transcription	NHLF	lung
17	chr1:183954200-183956400	Weak transcription	Brain Hippocampus Middle	brain
18	chr1:183954400-183956800	Weak transcription	Brain Substantia Nigra	brain
19	chr1:183954800-183956800	Enhancers	K562	blood
20	chr1:183955000-183956800	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr1:183955000-183959000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:183955000-183971200	Weak transcription	Right Atrium	heart
23	chr1:183955200-183955600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr1:183955200-183958800	Weak transcription	HepG2	liver
25	chr1:183955400-183955800	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr1:183955600-183958800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr1:183955800-183958800	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr1:183955800-183959000	Enhancers	HSMM	muscle
29	chr1:183956000-183956200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr1:183956000-183956600	Enhancers	NH-A	brain
31	chr1:183956000-183956800	Enhancers	Fetal Heart	heart
32	chr1:183956000-183956800	Enhancers	HSMMtube	muscle
33	chr1:183956000-183958800	Enhancers	Brain Cingulate Gyrus	brain
34	chr1:183956000-183958800	Enhancers	NHLF	lung
35	chr1:183956000-183959600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr1:183956200-183958600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr1:183956200-183958800	Enhancers	Muscle Satellite Cultured Cells	--
38	chr1:183956400-183958400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr1:183956400-183958600	Enhancers	Brain Hippocampus Middle	brain
40	chr1:183956400-183958800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr1:183956400-183958800	Enhancers	Brain Angular Gyrus	brain
42	chr1:183956400-183958800	Enhancers	Osteobl	bone
43	chr1:183956600-183958400	Weak transcription	NH-A	brain
44	chr1:183956600-183958600	Enhancers	Brain Anterior Caudate	brain
45	chr1:183956800-183957000	Flanking Active TSS	Fetal Heart	heart
46	chr1:183956800-183957000	Enhancers	Psoas Muscle	Psoas
47	chr1:183956800-183957000	Enhancers	Stomach Mucosa	stomach
48	chr1:183956800-183957200	Flanking Active TSS	K562	blood
49	chr1:183956800-183957600	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr1:183956800-183958800	Enhancers	Brain Substantia Nigra	brain

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