Variant report

Variant	nsv599565
Chromosome Location	chr5:118661882-118691888
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1443)
CpG islands
(count:1098)
Chromatin interactive
region (count:41)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1443 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:118670705-118671029	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:118667440-118667954	K562	blood:	n/a	n/a
3	ARID3A	chr5:118664564-118664861	K562	blood:	n/a	n/a
4	ARID3A	chr5:118673259-118673296	K562	blood:	n/a	n/a
5	ARID3A	chr5:118665689-118666797	K562	blood:	n/a	n/a
6	ARID3A	chr5:118663927-118664031	K562	blood:	n/a	n/a
7	ARID3A	chr5:118675431-118676059	K562	blood:	n/a	n/a
8	ATF1	chr5:118670279-118670327	K562	blood:	n/a	n/a
9	ATF1	chr5:118667517-118667956	K562	blood:	n/a	n/a
10	ATF1	chr5:118677891-118678079	K562	blood:	n/a	n/a
11	ATF1	chr5:118679408-118679544	K562	blood:	n/a	n/a
12	ATF1	chr5:118676333-118677014	K562	blood:	n/a	n/a
13	ATF1	chr5:118665638-118666756	K562	blood:	n/a	n/a
14	ATF2	chr5:118689827-118690698	GM12878	blood:	n/a	n/a
15	ATF2	chr5:118670480-118670949	GM12878	blood:	n/a	n/a
16	ATF2	chr5:118691304-118692503	GM12878	blood:	n/a	n/a
17	ATF2	chr5:118689343-118690645	GM12878	blood:	n/a	n/a
18	ATF2	chr5:118662713-118663170	GM12878	blood:	n/a	n/a
19	ATF2	chr5:118679215-118679910	GM12878	blood:	n/a	n/a
20	ATF2	chr5:118667855-118669525	GM12878	blood:	n/a	n/a
21	ATF2	chr5:118675651-118678448	GM12878	blood:	n/a	n/a
22	ATF2	chr5:118679296-118679918	GM12878	blood:	n/a	n/a
23	ATF2	chr5:118675485-118677940	GM12878	blood:	n/a	n/a
24	ATF2	chr5:118691369-118691917	GM12878	blood:	n/a	n/a
25	ATF3	chr5:118665949-118666593	K562	blood:	n/a	n/a
26	BACH1	chr5:118682477-118682568	K562	blood:	n/a	n/a
27	BACH1	chr5:118662831-118663022	K562	blood:	n/a	n/a
28	BACH1	chr5:118668614-118668738	K562	blood:	n/a	n/a
29	BACH1	chr5:118690953-118691153	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr5:118685198-118685225	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr5:118679359-118679844	GM12878	blood:	n/a	n/a
32	BATF	chr5:118691509-118691818	GM12878	blood:	n/a	n/a
33	BATF	chr5:118676180-118676561	GM12878	blood:	n/a	n/a
34	BATF	chr5:118677370-118677893	GM12878	blood:	n/a	n/a
35	BATF	chr5:118668825-118669139	GM12878	blood:	n/a	n/a
36	BATF	chr5:118691377-118691933	GM12878	blood:	n/a	n/a
37	BCL11A	chr5:118677312-118677762	GM12878	blood:	n/a	chr5:118677543-118677552
38	BCL11A	chr5:118691327-118691910	GM12878	blood:	n/a	chr5:118691526-118691539 chr5:118691546-118691559 chr5:118691527-118691540
39	BCL11A	chr5:118677374-118677698	GM12878	blood:	n/a	chr5:118677543-118677552
40	BCL11A	chr5:118676114-118676728	GM12878	blood:	n/a	chr5:118676341-118676350
41	BCL11A	chr5:118676243-118676633	GM12878	blood:	n/a	chr5:118676341-118676350
42	BCL11A	chr5:118679324-118679822	GM12878	blood:	n/a	n/a
43	BCL3	chr5:118676124-118676678	GM12878	blood:	n/a	chr5:118676341-118676350
44	BCL3	chr5:118691275-118691906	GM12878	blood:	n/a	chr5:118691526-118691539 chr5:118691546-118691559 chr5:118691527-118691540
45	BCL3	chr5:118670601-118671129	A549	lung:	n/a	n/a
46	BCLAF1	chr5:118690659-118691201	GM12878	blood:	n/a	n/a
47	BCLAF1	chr5:118676780-118678155	GM12878	blood:	n/a	chr5:118677543-118677552
48	BCLAF1	chr5:118689518-118690235	GM12878	blood:	n/a	n/a
49	BCLAF1	chr5:118677006-118678110	GM12878	blood:	n/a	chr5:118677543-118677552
50	BCLAF1	chr5:118679311-118679762	GM12878	blood:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:118689961-118690011	SK-N-MC	brain:	n/a
2	chr5:118691561-118691611	SKMC	muscle:	n/a
3	chr5:118691126-118691176	SK-N-MC	brain:	n/a
4	chr5:118691033-118691083	AG04450	lung:	fetal
5	chr5:118691425-118691475	Jurkat	blood:	n/a
6	chr5:118691794-118691844	GM19239	blood:	n/a
7	chr5:118691794-118691844	LNCaP	prostate:	n/a
8	chr5:118689293-118689343	MCF10A-Er-Src	breast:	n/a
9	chr5:118677172-118677222	SK-N-SH	brain:	n/a
10	chr5:118690955-118691005	ProgFib	skin:	n/a
11	chr5:118691126-118691176	ECC-1	luminal epithelium:	n/a
12	chr5:118689961-118690011	BJ	skin:	n/a
13	chr5:118691126-118691176	AG09309	skin:	n/a
14	chr5:118691415-118691465	GM12891	blood:	n/a
15	chr5:118691425-118691475	GM06990	blood:	n/a
16	chr5:118691066-118691116	AG10803	skin:	n/a
17	chr5:118691007-118691057	NH-A	brain:	n/a
18	chr5:118691066-118691116	SK-N-SH	brain:	n/a
19	chr5:118683890-118683940	NB4	blood:	n/a
20	chr5:118683890-118683940	AG04449	skin:	fetal
21	chr5:118691697-118691747	T-47D	breast:	n/a
22	chr5:118683890-118683940	HMEC	breast:	n/a
23	chr5:118691415-118691465	HUVEC	blood vessel:	n/a
24	chr5:118691751-118691801	SK-N-MC	brain:	n/a
25	chr5:118691415-118691465	Jurkat	blood:	n/a
26	chr5:118691033-118691083	CMK	blood:	n/a
27	chr5:118691033-118691083	Jurkat	blood:	n/a
28	chr5:118691126-118691176	GM12892	blood:	n/a
29	chr5:118676053-118676103	RPTEC	kidney:	n/a
30	chr5:118683890-118683940	HepG2	liver:	n/a
31	chr5:118676053-118676103	SK-N-MC	brain:	n/a
32	chr5:118690955-118691005	Hela-S3	cervix:	n/a
33	chr5:118691794-118691844	AG09309	skin:	n/a
34	chr5:118689293-118689343	AG04449	skin:	fetal
35	chr5:118691033-118691083	HUVEC	blood vessel:	n/a
36	chr5:118676053-118676103	AG04450	lung:	fetal
37	chr5:118689961-118690011	NHDF-neo	bronchial:	n/a
38	chr5:118683890-118683940	PrEC	prostate:	n/a
39	chr5:118665275-118665325	HL-60	blood:	n/a
40	chr5:118691561-118691611	SAEC	small airway:	n/a
41	chr5:118689293-118689343	PFSK-1	brain:	n/a
42	chr5:118691415-118691465	HRE	kidney:	n/a
43	chr5:118691694-118691744	RPTEC	kidney:	n/a
44	chr5:118691425-118691475	NT2-D1	testis:	n/a
45	chr5:118691751-118691801	HCM	heart:	n/a
46	chr5:118691751-118691801	BE2_C	brain:	n/a
47	chr5:118691694-118691744	HEEpiC	esophagus:	n/a
48	chr5:118691697-118691747	BE2_C	brain:	n/a
49	chr5:118691751-118691801	CMK	blood:	n/a
50	chr5:118689293-118689343	MCF-7	breast:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:118667237..118669895-chr5:118670074..118672597,2	K562	blood:
2	chr5:118672680..118674679-chr5:118676635..118678463,2	K562	blood:
3	chr5:118650756..118653747-chr5:118669086..118671011,2	MCF-7	breast:
4	chr5:118668038..118668652-chr5:118747446..118748001,2	MCF-7	breast:
5	chr5:118623648..118626074-chr5:118666762..118668589,2	MCF-7	breast:
6	chr5:118657545..118660417-chr5:118661567..118663865,2	MCF-7	breast:
7	chr5:118665150..118667137-chr5:118667473..118670063,2	K562	blood:
8	chr5:118665304..118666908-chr5:118684151..118685664,2	K562	blood:
9	chr5:118662612..118665528-chr5:118665801..118667898,2	MCF-7	breast:
10	chr5:118405258..118407734-chr5:118663807..118667698,3	K562	blood:
11	chr5:118626131..118628093-chr5:118660275..118662389,2	K562	blood:
12	chr5:118672680..118674679-chr5:118676635..118678463,2	K562	blood:
13	chr5:118643237..118645769-chr5:118664741..118667190,3	K562	blood:
14	chr5:118636247..118638488-chr5:118660209..118662344,2	K562	blood:
15	chr5:118669449..118670965-chr5:118681990..118684958,2	K562	blood:
16	chr5:118671639..118673344-chr5:118704484..118706218,2	MCF-7	breast:
17	chr5:118547322..118548106-chr5:118670433..118671294,2	MCF-7	breast:
18	chr5:118651451..118652140-chr5:118670433..118670936,2	MCF-7	breast:
19	chr5:118686914..118688782-chr5:118689065..118691768,2	MCF-7	breast:
20	chr5:118623079..118625774-chr5:118657977..118661910,3	MCF-7	breast:
21	chr5:118662612..118665528-chr5:118665801..118667898,2	MCF-7	breast:
22	chr5:118666728..118668661-chr5:118669320..118670898,2	MCF-7	breast:
23	chr5:118669449..118670965-chr5:118681990..118684958,2	K562	blood:
24	chr5:118675434..118678874-chr5:118679948..118684456,6	K562	blood:
25	chr5:118602762..118604388-chr5:118664246..118665991,2	MCF-7	breast:
26	chr5:118626131..118628093-chr5:118660275..118663630,3	K562	blood:
27	chr5:118602801..118604637-chr5:118670249..118672077,2	MCF-7	breast:
28	chr5:118322596..118324427-chr5:118669439..118671541,2	MCF-7	breast:
29	chr5:118603982..118606097-chr5:118661262..118663563,2	MCF-7	breast:
30	chr5:118666448..118669414-chr5:118669488..118671183,2	MCF-7	breast:
31	chr5:118654543..118656491-chr5:118674624..118677344,2	K562	blood:
32	chr5:118666728..118668661-chr5:118669320..118670898,2	MCF-7	breast:
33	chr5:118604157..118605993-chr5:118671344..118674136,2	MCF-7	breast:
34	chr5:118658870..118659716-chr5:118670433..118671147,2	MCF-7	breast:
35	chr5:118660112..118661671-chr5:118661964..118664780,2	MCF-7	breast:
36	chr5:118657976..118659657-chr5:118675627..118677194,2	MCF-7	breast:
37	chr5:118405258..118407472-chr5:118664950..118669105,3	K562	blood:
38	chr5:118675434..118678874-chr5:118679948..118684456,6	K562	blood:
39	chr5:118665304..118666908-chr5:118684151..118685664,2	K562	blood:
40	chr5:118670103..118672210-chr5:118744741..118746294,2	MCF-7	breast:
41	chr5:118666908..118671699-chr5:118672968..118679055,7	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMXL1-8	chr5:118677271-118680524	NONHSAT103433

No data

Variant related genes	Relation type
TNFAIP8	TF binding region
TNFAIP8	CpG island
ENSG00000249494	chromatin interactions
ENSG00000145779	chromatin interactions
ENSG00000169570	chromatin interactions
ENSG00000172869	chromatin interactions

Extended variants
information (count: 1173 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1173 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2052473	chr5:118661882-118661883	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562975306	chr5:118661885-118661886	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs547648897	chr5:118661887-118661888	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs11747473	chr5:118661902-118661903	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs567537079	chr5:118661912-118661913	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs530267140	chr5:118661936-118661937	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550041627	chr5:118661948-118661949	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs35420099	chr5:118662001-118662002	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs531755999	chr5:118662002-118662003	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs115720812	chr5:118662035-118662036	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs558911005	chr5:118662052-118662053	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs149340853	chr5:118662058-118662059	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs535132999	chr5:118662076-118662077	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs34533125	chr5:118662087-118662088	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs554798313	chr5:118662090-118662091	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559753067	chr5:118662096-118662097	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs371327158	chr5:118662101-118662102	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs186281130	chr5:118662113-118662114	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs144668515	chr5:118662133-118662134	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs10073635	chr5:118662178-118662179	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs190798776	chr5:118662225-118662226	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs569061985	chr5:118662253-118662254	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs377586966	chr5:118662256-118662257	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs545441236	chr5:118662299-118662300	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs370840822	chr5:118662303-118662304	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs548591139	chr5:118662310-118662311	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs568423488	chr5:118662345-118662346	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs539691157	chr5:118662375-118662376	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs551433927	chr5:118662390-118662391	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs376926606	chr5:118662397-118662398	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs55928915	chr5:118662432-118662433	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs183893197	chr5:118662502-118662503	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs148516086	chr5:118662503-118662504	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs561478228	chr5:118662575-118662576	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs530219342	chr5:118662596-118662597	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs566477502	chr5:118662619-118662620	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550004765	chr5:118662637-118662638	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs141892390	chr5:118662665-118662666	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs531615543	chr5:118662668-118662669	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs34783586	chr5:118662684-118662685	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs397883797	chr5:118662687-118662688	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs532857688	chr5:118662714-118662715	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs147283846	chr5:118662719-118662720	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs566044094	chr5:118662740-118662741	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs373159084	chr5:118662743-118662744	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs201005953	chr5:118662768-118662769	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs116583883	chr5:118662821-118662822	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs186482973	chr5:118662835-118662836	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs140464544	chr5:118662883-118662884	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs190523943	chr5:118662884-118662885	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Prostate cancer	22341455	CNVD
Gastric cancer	17229543	CNVD

Chromatin state (count:1570 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118645200-118664000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
2	chr5:118648000-118664600	Enhancers	Primary B cells from peripheral blood	blood
3	chr5:118650000-118664000	Weak transcription	Rectal Smooth Muscle	rectum
4	chr5:118651400-118662000	Weak transcription	Fetal Stomach	stomach
5	chr5:118653800-118663000	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr5:118654400-118663400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr5:118655000-118664600	Enhancers	Thymus	Thymus
8	chr5:118655600-118662600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr5:118655600-118663200	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr5:118656400-118663000	Enhancers	Placenta	Placenta
11	chr5:118656600-118664400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr5:118657200-118663200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr5:118657200-118665200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr5:118657200-118665400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr5:118657400-118663200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr5:118657400-118664000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:118657600-118664200	Weak transcription	Stomach Smooth Muscle	stomach
18	chr5:118657600-118665200	Enhancers	NH-A	brain
19	chr5:118657800-118664800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr5:118658200-118670400	Weak transcription	Lung	lung
21	chr5:118658400-118663800	Weak transcription	Fetal Lung	lung
22	chr5:118658800-118665600	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr5:118659200-118664600	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr5:118659600-118662400	Weak transcription	Small Intestine	intestine
25	chr5:118659600-118663800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr5:118659600-118664000	Weak transcription	HSMM	muscle
27	chr5:118659600-118664200	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr5:118659600-118664200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr5:118659600-118664600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:118659600-118677800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr5:118660000-118664600	Weak transcription	Colonic Mucosa	Colon
32	chr5:118660200-118663800	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr5:118660200-118664000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr5:118660200-118664200	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr5:118660200-118666600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr5:118660200-118675600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr5:118660200-118678600	Weak transcription	HepG2	liver
38	chr5:118660400-118662200	Enhancers	K562	blood
39	chr5:118660400-118662400	Enhancers	Primary T cells from cord blood	blood
40	chr5:118660400-118662600	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr5:118660400-118662600	Enhancers	Fetal Thymus	thymus
42	chr5:118660400-118662600	Weak transcription	Stomach Mucosa	stomach
43	chr5:118660400-118663800	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr5:118660400-118663800	Enhancers	Dnd41	blood
45	chr5:118660400-118664000	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr5:118660400-118664200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr5:118660400-118664600	Enhancers	GM12878-XiMat	blood
48	chr5:118660400-118666000	Enhancers	Adipose Nuclei	Adipose
49	chr5:118660400-118668600	Enhancers	Primary hematopoietic stem cells	blood
50	chr5:118660400-118670400	Weak transcription	Right Atrium	heart

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