Variant report

Variant	nsv1020910
Chromosome Location	chr5:42929799-43000021
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2530)
CpG islands
(count:3299)
Chromatin interactive
region (count:108)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2530 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:42992168-42992548	K562	blood:	n/a	n/a
2	ARID3A	chr5:42985717-42985775	K562	blood:	n/a	n/a
3	ARID3A	chr5:42986836-42987079	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:42985487-42986024	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:42986750-42987157	K562	blood:	n/a	n/a
6	ARID3A	chr5:42982241-42982769	K562	blood:	n/a	n/a
7	ATF1	chr5:42982124-42982317	K562	blood:	n/a	n/a
8	ATF1	chr5:42986728-42987158	K562	blood:	n/a	n/a
9	ATF2	chr5:42994547-42995455	GM12878	blood:	n/a	n/a
10	ATF2	chr5:42951212-42951966	GM12878	blood:	n/a	n/a
11	ATF2	chr5:42991792-42992458	GM12878	blood:	n/a	n/a
12	ATF2	chr5:42993779-42994544	GM12878	blood:	n/a	n/a
13	ATF2	chr5:42992858-42993694	GM12878	blood:	n/a	n/a
14	ATF2	chr5:42993914-42994627	GM12878	blood:	n/a	n/a
15	ATF2	chr5:42993159-42993736	GM12878	blood:	n/a	n/a
16	ATF2	chr5:42991454-42992732	GM12878	blood:	n/a	n/a
17	ATF2	chr5:42950606-42951226	GM12878	blood:	n/a	n/a
18	ATF2	chr5:42994704-42995377	GM12878	blood:	n/a	n/a
19	ATF2	chr5:42992072-42992367	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr5:42949154-42949925	GM12878	blood:	n/a	n/a
21	ATF3	chr5:42950771-42951048	K562	blood:	n/a	n/a
22	ATF3	chr5:42950670-42951165	A549	lung:	n/a	n/a
23	ATF3	chr5:42994544-42995361	A549	lung:	n/a	n/a
24	ATF3	chr5:42950560-42951133	K562	blood:	n/a	n/a
25	ATF3	chr5:42985277-42985965	HCT-116	colon:	n/a	n/a
26	ATF3	chr5:42950578-42951218	A549	lung:	n/a	n/a
27	ATF3	chr5:42993249-42993693	K562	blood:	n/a	chr5:42993483-42993497
28	BACH1	chr5:42950556-42951123	H1-hESC	embryonic stem cell:	n/a	chr5:42950925-42950939
29	BACH1	chr5:42992078-42992427	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr5:42991476-42991672	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr5:42993295-42993491	K562	blood:	n/a	n/a
32	BACH1	chr5:42991675-42991967	K562	blood:	n/a	n/a
33	BACH1	chr5:42992251-42992407	K562	blood:	n/a	n/a
34	BACH1	chr5:42987886-42988025	K562	blood:	n/a	n/a
35	BACH1	chr5:42993932-42994615	K562	blood:	n/a	n/a
36	BATF	chr5:42991822-42992534	GM12878	blood:	n/a	n/a
37	BATF	chr5:42950689-42951086	GM12878	blood:	n/a	chr5:42950913-42950923
38	BATF	chr5:42993219-42993670	GM12878	blood:	n/a	chr5:42993484-42993494 chr5:42993483-42993494
39	BATF	chr5:42993300-42993567	GM12878	blood:	n/a	chr5:42993484-42993494 chr5:42993483-42993494
40	BATF	chr5:42951293-42951654	GM12878	blood:	n/a	n/a
41	BCL11A	chr5:42993279-42993608	GM12878	blood:	n/a	chr5:42993483-42993492
42	BCL11A	chr5:42991887-42992687	GM12878	blood:	n/a	n/a
43	BCL3	chr5:42994623-42995512	A549	lung:	n/a	n/a
44	BCL3	chr5:42950428-42951167	A549	lung:	n/a	n/a
45	BCL3	chr5:42993088-42993571	A549	lung:	n/a	chr5:42993483-42993492
46	BCL3	chr5:42992091-42992746	A549	lung:	n/a	n/a
47	BCL3	chr5:42950586-42951217	A549	lung:	n/a	chr5:42951207-42951216
48	BCL3	chr5:42994743-42995447	A549	lung:	n/a	n/a
49	BCLAF1	chr5:42951939-42952479	GM12878	blood:	n/a	n/a
50	BCLAF1	chr5:42950842-42952328	GM12878	blood:	n/a	chr5:42951473-42951486 chr5:42951473-42951486 chr5:42951233-42951246 chr5:42951286-42951295 chr5:42951207-42951216 chr5:42951287-42951300 chr5:42951289-42951298

(count:3299 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:42950062-42950112	PANC-1	pancreas:	n/a
2	chr5:42992998-42993048	IMR90	lung:	fetal
3	chr5:42950785-42950835	GM06990	blood:	n/a
4	chr5:42951346-42951396	K562	blood:	n/a
5	chr5:42991862-42991912	HEK293	kidney:	embryo
6	chr5:42950062-42950112	PANC-1	pancreas:	n/a
7	chr5:42992998-42993048	IMR90	lung:	fetal
8	chr5:42950785-42950835	GM06990	blood:	n/a
9	chr5:42951346-42951396	K562	blood:	n/a
10	chr5:42991862-42991912	HEK293	kidney:	embryo
11	chr5:42949882-42949932	K562	blood:	n/a
12	chr5:42991657-42991707	BE2_C	brain:	n/a
13	chr5:42944457-42944507	HPAEpiC	pulmonary alveolar:	n/a
14	chr5:42970699-42970749	AG04449	skin:	fetal
15	chr5:42993450-42993500	NH-A	brain:	n/a
16	chr5:42972820-42972870	GM06990	blood:	n/a
17	chr5:42949799-42949849	HRPEpiC	eye:	n/a
18	chr5:42944030-42944080	HPAEpiC	pulmonary alveolar:	n/a
19	chr5:42998521-42998571	PFSK-1	brain:	n/a
20	chr5:42995203-42995253	BE2_C	brain:	n/a
21	chr5:42944030-42944080	NT2-D1	testis:	n/a
22	chr5:42971223-42971273	NB4	blood:	n/a
23	chr5:42993440-42993490	GM12891	blood:	n/a
24	chr5:42941518-42941568	HCPEpiC	choroid plexus:	n/a
25	chr5:42951192-42951242	HCT-116	colon:	n/a
26	chr5:42949799-42949849	U87	brain:	n/a
27	chr5:42993450-42993500	HMEC	breast:	n/a
28	chr5:42995527-42995577	A549	lung:	n/a
29	chr5:42945163-42945213	Hepatocyte	liver:	n/a
30	chr5:42993978-42994028	PANC-1	pancreas:	n/a
31	chr5:42949542-42949592	HNPCEpiC	eye:	n/a
32	chr5:42951346-42951396	NT2-D1	testis:	n/a
33	chr5:42993450-42993500	GM12892	blood:	n/a
34	chr5:42995369-42995419	K562	blood:	n/a
35	chr5:42998521-42998571	SK-N-SH	brain:	n/a
36	chr5:42992128-42992178	NB4	blood:	n/a
37	chr5:42995123-42995173	ECC-1	luminal epithelium:	n/a
38	chr5:42992555-42992605	GM12892	blood:	n/a
39	chr5:42943857-42943907	LNCaP	prostate:	n/a
40	chr5:42944457-42944507	PANC-1	pancreas:	n/a
41	chr5:42995203-42995253	ECC-1	luminal epithelium:	n/a
42	chr5:42952369-42952419	AG09309	skin:	n/a
43	chr5:42993450-42993500	GM06990	blood:	n/a
44	chr5:42945163-42945213	SK-N-SH_RA	brain:	n/a
45	chr5:42994776-42994826	GM19239	blood:	n/a
46	chr5:42949542-42949592	HRE	kidney:	n/a
47	chr5:42951192-42951242	AoSMC	blood vessel:	n/a
48	chr5:42953624-42953674	K562	blood:	n/a
49	chr5:42950152-42950202	ECC-1	luminal epithelium:	n/a
50	chr5:42944494-42944544	HCF	heart:	n/a

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:42969037..42971723-chr5:42975649..42977780,2	K562	blood:
2	chr5:42958938..42960616-chr5:42961964..42963478,2	MCF-7	breast:
3	chr5:42939089..42940720-chr5:42941023..42943265,2	MCF-7	breast:
4	chr15:65587975..65588974-chr5:42950581..42951338,2	Hela-S3	cervix:
5	chr17:56708499..56709346-chr5:42992938..42993491,2	Hela-S3	cervix:
6	chr5:42991975..42992808-chr5:43007900..43008580,2	NB4	blood:
7	chr5:42990973..42999044-chr5:43062393..43068169,17	K562	blood:
8	chr1:202926733..202927516-chr5:42992240..42992746,2	Hela-S3	cervix:
9	chr1:153962914..153963746-chr5:42992072..42992592,2	NB4	blood:
10	chr5:42948996..42951624-chr5:43068211..43070769,2	MCF-7	breast:
11	chr5:6632723..6633278-chr5:42991235..42991736,2	Hela-S3	cervix:
12	chr5:42949769..42951285-chr5:42989512..42991530,2	K562	blood:
13	chr5:42992332..42993325-chr7:140396349..140397168,2	Hela-S3	cervix:
14	chr5:42992079..42993049-chr5:43041048..43041754,2	Hela-S3	cervix:
15	chr5:42974190..42975842-chr5:42991638..42994075,2	MCF-7	breast:
16	chr5:42946321..42948335-chr5:43066573..43068455,2	K562	blood:
17	chr5:42976709..42980767-chr5:43006838..43010381,4	K562	blood:
18	chr1:249167058..249167599-chr5:42950376..42951299,2	Hela-S3	cervix:
19	chr15:41047428..41048122-chr5:42992753..42993556,2	Hela-S3	cervix:
20	chr5:42993139..42993641-chr5:43040150..43041114,2	K562	blood:
21	chr5:42989588..43001279-chr5:43004636..43014428,32	K562	blood:
22	chr5:42930977..42933954-chr5:42950606..42953206,2	MCF-7	breast:
23	chr17:8023704..8024472-chr5:42950367..42950876,2	Hela-S3	cervix:
24	chr5:41924886..41927114-chr5:42991951..42994899,2	K562	blood:
25	chr5:42939089..42940720-chr5:42941023..42943265,2	MCF-7	breast:
26	chr5:42986506..42989376-chr5:43041459..43043434,3	K562	blood:
27	chr5:42941021..42945683-chr5:42991872..42995259,5	K562	blood:
28	chr5:42949769..42951285-chr5:42989512..42991530,2	K562	blood:
29	chr5:42996039..42998077-chr5:43007869..43010510,2	MCF-7	breast:
30	chr1:149815015..149815766-chr5:42992813..42993512,2	Hela-S3	cervix:
31	chr5:42994652..42996871-chr5:43105565..43107104,2	K562	blood:
32	chr5:42975954..42977649-chr5:43041510..43043322,2	K562	blood:
33	chr5:42950507..42951264-chr5:134475534..134476311,2	Hela-S3	cervix:
34	chr18:44676633..44677401-chr5:42950458..42951078,2	Hela-S3	cervix:
35	chr5:42992357..42992951-chr6:26158187..26158692,2	Hela-S3	cervix:
36	chr5:42991772..42994897-chr5:42997978..43001031,3	MCF-7	breast:
37	chr5:42992046..42992772-chr5:43041551..43042168,2	NB4	blood:
38	chr5:42992038..42994724-chr5:43120190..43122287,2	K562	blood:
39	chr18:45663149..45664043-chr5:42992293..42992947,2	Hela-S3	cervix:
40	chr5:42904231..42907156-chr5:42940925..42943861,2	K562	blood:
41	chr10:60027527..60028389-chr5:42994884..42995400,2	Hela-S3	cervix:
42	chr5:42928813..42931600-chr5:43007922..43010335,2	MCF-7	breast:
43	chr5:42998105..43003044-chr5:43016342..43020590,4	MCF-7	breast:
44	chr1:156022915..156023691-chr5:42992111..42993091,2	NB4	blood:
45	chr5:42994273..42995054-chr5:43018174..43018755,2	Hela-S3	cervix:
46	chr11:66056545..66057202-chr5:42950293..42951110,2	Hela-S3	cervix:
47	chr5:42909564..42912541-chr5:42988182..42990519,2	K562	blood:
48	chr5:42984356..42986139-chr5:43039157..43041117,2	K562	blood:
49	chr5:42958938..42960616-chr5:42961964..42963478,2	MCF-7	breast:
50	chr5:42961475..42963380-chr5:42978584..42980242,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf39-7	chr5:42971231-42971776	NONHSAT101239
2	lnc-C5orf39-2	chr5:42985555-42985625	XLOC_004803
3	lnc-C5orf39-2	chr5:42990941-42991008	XLOC_004803
4	lnc-C5orf39-2	chr5:42985140-42985764	XLOC_004803
5	lnc-C5orf39-2	chr5:42991255-42992726	XLOC_004803
6	lnc-C5orf39-2	chr5:42990941-42991348	XLOC_004803
7	lnc-ZNF131-4	chr5:42950963-42959174	XLOC_004362
8	lnc-ZNF131-4	chr5:42960426-42960649	XLOC_004362
9	lnc-C5orf39-2	chr5:42985708-42985764	XLOC_004803

No data

Variant related genes	Relation type
ENSG00000250711	TF binding region
ENSG00000250711	CpG island
ENSG00000212195	chromatin interactions
ENSG00000152147	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000215068	chromatin interactions
ENSG00000037474	chromatin interactions
ENSG00000148950	chromatin interactions
ENSG00000167220	chromatin interactions
ENSG00000151151	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000177426	chromatin interactions
ENSG00000177721	chromatin interactions
ENSG00000160803	chromatin interactions
ENSG00000128989	chromatin interactions
ENSG00000240889	chromatin interactions
ENSG00000162676	chromatin interactions
ENSG00000130164	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000131508	chromatin interactions
ENSG00000177738	chromatin interactions
ENSG00000184828	chromatin interactions
ENSG00000271788	chromatin interactions
ENSG00000090266	chromatin interactions
ENSG00000109911	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000151876	chromatin interactions
ENSG00000251131	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000163584	chromatin interactions
ENSG00000172262	chromatin interactions
ENSG00000272144	chromatin interactions
ENSG00000137824	chromatin interactions
ENSG00000159346	chromatin interactions
ENSG00000177954	chromatin interactions
ENSG00000105321	chromatin interactions
E2F6	miRNA target sites

Extended variants
information (count: 2878 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2878 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576228509	chr5:42929869-42929870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs182779823	chr5:42929883-42929884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536685175	chr5:42929951-42929952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561849004	chr5:42930028-42930029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529000727	chr5:42930055-42930056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs77379234	chr5:42930070-42930071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs559399076	chr5:42930128-42930129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532905759	chr5:42930143-42930144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72759102	chr5:42930149-42930150	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs150984017	chr5:42930165-42930166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531964081	chr5:42930176-42930177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142213860	chr5:42930189-42930190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568607166	chr5:42930203-42930204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376514967	chr5:42930218-42930219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2603630	chr5:42930258-42930259	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs554410226	chr5:42930259-42930260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565782874	chr5:42930285-42930286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2603629	chr5:42930289-42930290	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs528202023	chr5:42930302-42930303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188433852	chr5:42930315-42930316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555378922	chr5:42930364-42930365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548639275	chr5:42930366-42930367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs370005830	chr5:42930381-42930382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146395609	chr5:42930382-42930383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs6881470	chr5:42930385-42930386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs75196275	chr5:42930387-42930388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs73751298	chr5:42930417-42930418	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs193237552	chr5:42930418-42930419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572749856	chr5:42930438-42930439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573737966	chr5:42930444-42930445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541129063	chr5:42930445-42930446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544151298	chr5:42930478-42930479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568004542	chr5:42930489-42930490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs145284047	chr5:42930490-42930491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147858288	chr5:42930510-42930511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563718195	chr5:42930533-42930534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532995067	chr5:42930552-42930553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545001047	chr5:42930576-42930577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2603628	chr5:42930664-42930665	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs531929895	chr5:42930667-42930668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550410972	chr5:42930670-42930671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563222484	chr5:42930682-42930683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530407311	chr5:42930736-42930737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141411591	chr5:42930745-42930746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79122555	chr5:42930774-42930775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185664056	chr5:42930776-42930777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539855297	chr5:42930787-42930788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373329362	chr5:42930851-42930852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551506787	chr5:42930871-42930872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569998028	chr5:42930912-42930913	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	21364760	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelofibrosis	22110671	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Lung cancer	21569311	CNVD

Chromatin state (count:1731 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:42929800-42930200	Enhancers	HUVEC	blood vessel
2	chr5:42930000-42931200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr5:42930000-42931200	Enhancers	NHEK	skin
4	chr5:42930000-42931600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:42930600-42931000	Enhancers	HMEC	breast
6	chr5:42932000-42932800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:42940200-42940400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr5:42940200-42940800	Enhancers	A549	lung
9	chr5:42940400-42941600	Enhancers	HepG2	liver
10	chr5:42940400-42948800	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr5:42940600-42940800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr5:42940800-42941400	Flanking Active TSS	A549	lung
13	chr5:42940800-42944000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr5:42941400-42941800	Enhancers	A549	lung
15	chr5:42941400-42942200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr5:42941800-42942800	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr5:42941800-42945200	Weak transcription	A549	lung
18	chr5:42943400-42943600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr5:42943400-42944200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
20	chr5:42943600-42943800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr5:42943600-42943800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr5:42943600-42943800	Active TSS	NH-A	brain
23	chr5:42943600-42943800	Enhancers	NHDF-Ad	bronchial
24	chr5:42943600-42943800	Enhancers	NHLF	lung
25	chr5:42943600-42943800	Enhancers	Osteobl	bone
26	chr5:42943600-42944000	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr5:42943600-42944600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:42943600-42944800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr5:42943800-42944000	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr5:42943800-42944000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr5:42943800-42944000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
32	chr5:42943800-42944000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
33	chr5:42943800-42944000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr5:42943800-42944000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr5:42943800-42944000	Enhancers	Muscle Satellite Cultured Cells	--
36	chr5:42943800-42944000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
37	chr5:42943800-42944000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr5:42943800-42944000	Enhancers	Adipose Nuclei	Adipose
39	chr5:42943800-42944000	Bivalent Enhancer	Brain Anterior Caudate	brain
40	chr5:42943800-42944000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
41	chr5:42943800-42944000	Flanking Active TSS	NH-A	brain
42	chr5:42943800-42944000	Flanking Active TSS	NHDF-Ad	bronchial
43	chr5:42943800-42944200	Bivalent Enhancer	Brain Angular Gyrus	brain
44	chr5:42943800-42944200	Bivalent Enhancer	Colon Smooth Muscle	Colon
45	chr5:42943800-42944400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
46	chr5:42943800-42944400	Bivalent Enhancer	Brain Cingulate Gyrus	brain
47	chr5:42943800-42944400	Bivalent Enhancer	Brain Substantia Nigra	brain
48	chr5:42943800-42944600	Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr5:42943800-42944600	Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr5:42943800-42944600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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