Variant report

Variant	nsv872529
Chromosome Location	chr1:168343349-168384168
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:767)
CpG islands
(count:489)
Chromatin interactive
region (count:35)
LncRNA
region (count:7)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:767 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:168368098-168368571	K562	blood:	n/a	n/a
2	ARID3A	chr1:168368284-168368533	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:168378059-168378372	K562	blood:	n/a	chr1:168378107-168378123
4	ARID3A	chr1:168343229-168343407	K562	blood:	n/a	n/a
5	ARID3A	chr1:168378183-168378313	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:168371924-168371935	K562	blood:	n/a	n/a
7	ATF1	chr1:168378142-168378410	K562	blood:	n/a	n/a
8	ATF1	chr1:168373187-168373436	K562	blood:	n/a	n/a
9	ATF1	chr1:168343203-168343424	K562	blood:	n/a	n/a
10	ATF1	chr1:168377170-168377200	K562	blood:	n/a	n/a
11	ATF2	chr1:168356434-168356843	H1-hESC	embryonic stem cell:	n/a	chr1:168356575-168356589 chr1:168356577-168356588
12	ATF2	chr1:168356361-168357102	H1-hESC	embryonic stem cell:	n/a	chr1:168356575-168356589 chr1:168356577-168356588
13	ATF3	chr1:168368138-168368658	K562	blood:	n/a	n/a
14	ATF3	chr1:168377592-168378665	HCT-116	colon:	n/a	chr1:168378273-168378287
15	ATF3	chr1:168368315-168368701	K562	blood:	n/a	n/a
16	ATF3	chr1:168343126-168343426	K562	blood:	n/a	n/a
17	ATF3	chr1:168355801-168356057	K562	blood:	n/a	n/a
18	ATF3	chr1:168378036-168378503	K562	blood:	n/a	chr1:168378273-168378287
19	BACH1	chr1:168368283-168368645	H1-hESC	embryonic stem cell:	n/a	chr1:168368437-168368451
20	BACH1	chr1:168361870-168362573	K562	blood:	n/a	chr1:168362330-168362344
21	BACH1	chr1:168356174-168356821	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr1:168362166-168362509	H1-hESC	embryonic stem cell:	n/a	chr1:168362330-168362344
23	BACH1	chr1:168368271-168368612	K562	blood:	n/a	chr1:168368437-168368451
24	BACH1	chr1:168361902-168361929	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr1:168357056-168357360	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr1:168376500-168376541	K562	blood:	n/a	n/a
27	BATF	chr1:168378115-168378443	GM12878	blood:	n/a	chr1:168378273-168378284 chr1:168378253-168378263 chr1:168378274-168378284 chr1:168378252-168378263
28	BATF	chr1:168378152-168378447	GM12878	blood:	n/a	chr1:168378273-168378284 chr1:168378253-168378263 chr1:168378274-168378284 chr1:168378252-168378263
29	BCL11A	chr1:168379657-168379970	GM12878	blood:	n/a	n/a
30	BCL3	chr1:168348281-168348839	A549	lung:	n/a	chr1:168348563-168348572 chr1:168348562-168348571
31	BHLHE40	chr1:168379683-168380026	GM12878	blood:	n/a	n/a
32	BHLHE40	chr1:168367875-168367885	K562	blood:	n/a	n/a
33	BHLHE40	chr1:168347732-168348156	K562	blood:	n/a	n/a
34	BHLHE40	chr1:168343187-168343406	K562	blood:	n/a	n/a
35	BHLHE40	chr1:168362300-168362316	K562	blood:	n/a	n/a
36	BHLHE40	chr1:168371828-168371933	K562	blood:	n/a	n/a
37	BHLHE40	chr1:168368298-168368602	K562	blood:	n/a	n/a
38	BRCA1	chr1:168366205-168366816	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr1:168377700-168378424	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr1:168379159-168379169	GM12878	blood:	n/a	n/a
41	BRCA1	chr1:168375019-168375412	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr1:168361083-168361740	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr1:168359647-168359700	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr1:168356568-168356732	Hela-S3	cervix:	n/a	n/a
45	CBX3	chr1:168368139-168368604	K562	blood:	n/a	n/a
46	CBX3	chr1:168374736-168375745	HCT-116	colon:	n/a	n/a
47	CBX3	chr1:168377468-168378689	HCT-116	colon:	n/a	n/a
48	CBX3	chr1:168377435-168379361	HCT-116	colon:	n/a	n/a
49	CCNT2	chr1:168343207-168343407	K562	blood:	n/a	n/a
50	CCNT2	chr1:168356471-168356697	K562	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:168356537-168356587	BE2_C	brain:	n/a
2	chr1:168356537-168356587	BE2_C	brain:	n/a
3	chr1:168356673-168356723	MCF-7	breast:	n/a
4	chr1:168344184-168344234	HL-60	blood:	n/a
5	chr1:168343339-168343389	HMEC	breast:	n/a
6	chr1:168356591-168356641	HCF	heart:	n/a
7	chr1:168356591-168356641	NT2-D1	testis:	n/a
8	chr1:168343339-168343389	LNCaP	prostate:	n/a
9	chr1:168344264-168344314	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:168344264-168344314	A549	lung:	n/a
11	chr1:168356606-168356656	HCM	heart:	n/a
12	chr1:168344264-168344314	K562	blood:	n/a
13	chr1:168344264-168344314	Hela-S3	cervix:	n/a
14	chr1:168356537-168356587	SK-N-SH	brain:	n/a
15	chr1:168356673-168356723	PFSK-1	brain:	n/a
16	chr1:168356591-168356641	AG09309	skin:	n/a
17	chr1:168356591-168356641	HUVEC	blood vessel:	n/a
18	chr1:168343945-168343995	A549	lung:	n/a
19	chr1:168343339-168343389	AG10803	skin:	n/a
20	chr1:168356673-168356723	NHDF-neo	bronchial:	n/a
21	chr1:168356537-168356587	K562	blood:	n/a
22	chr1:168356673-168356723	HL-60	blood:	n/a
23	chr1:168356606-168356656	MCF10A-Er-Src	breast:	n/a
24	chr1:168343945-168343995	U87	brain:	n/a
25	chr1:168356537-168356587	BJ	skin:	n/a
26	chr1:168343339-168343389	PANC-1	pancreas:	n/a
27	chr1:168344184-168344234	SK-N-SH	brain:	n/a
28	chr1:168344264-168344314	AG10803	skin:	n/a
29	chr1:168356591-168356641	HCT-116	colon:	n/a
30	chr1:168356673-168356723	GM06990	blood:	n/a
31	chr1:168343945-168343995	AoSMC	blood vessel:	n/a
32	chr1:168344184-168344234	AG04449	skin:	fetal
33	chr1:168343339-168343389	HCM	heart:	n/a
34	chr1:168343339-168343389	GM19239	blood:	n/a
35	chr1:168356537-168356587	HCM	heart:	n/a
36	chr1:168343339-168343389	MCF10A-Er-Src	breast:	n/a
37	chr1:168356606-168356656	HRE	kidney:	n/a
38	chr1:168356673-168356723	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:168343945-168343995	HRCEpiC	kidney:	n/a
40	chr1:168343339-168343389	HUVEC	blood vessel:	n/a
41	chr1:168344264-168344314	HMEC	breast:	n/a
42	chr1:168343339-168343389	BJ	skin:	n/a
43	chr1:168356606-168356656	HUVEC	blood vessel:	n/a
44	chr1:168344264-168344314	ProgFib	skin:	n/a
45	chr1:168343945-168343995	SK-N-MC	brain:	n/a
46	chr1:168356537-168356587	SK-N-MC	brain:	n/a
47	chr1:168343945-168343995	MCF10A-Er-Src	breast:	n/a
48	chr1:168356537-168356587	HIPEpiC	eye:	n/a
49	chr1:168344264-168344314	HL-60	blood:	n/a
50	chr1:168356537-168356587	MCF-7	breast:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:168360896..168362544-chr1:168366659..168368237,2	K562	blood:
2	chr1:168360896..168362544-chr1:168366659..168368237,2	K562	blood:
3	chr1:168335359..168337795-chr1:168345574..168348326,2	K562	blood:
4	chr1:168349449..168351805-chr1:168370757..168373468,2	K562	blood:
5	chr1:168349449..168351805-chr1:168370757..168373468,2	K562	blood:
6	chr1:168348118..168353414-chr1:168355151..168359007,7	MCF-7	breast:
7	chr1:168366951..168368452-chr1:168372047..168373905,2	K562	blood:
8	chr1:168368481..168370115-chr1:168372441..168374527,2	K562	blood:
9	chr1:168344082..168345767-chr1:168346742..168349715,2	K562	blood:
10	chr1:168372698..168375484-chr1:168376700..168379733,3	K562	blood:
11	chr1:168346129..168348064-chr1:168353010..168355199,2	K562	blood:
12	chr1:168341145..168343864-chr1:168357058..168358969,2	K562	blood:
13	chr1:168355026..168356826-chr1:168398882..168401309,2	K562	blood:
14	chr1:168357609..168359334-chr1:168366941..168369901,2	K562	blood:
15	chr1:168338940..168340901-chr1:168341151..168343365,2	MCF-7	breast:
16	chr1:168342866..168344756-chr1:168372914..168374516,2	K562	blood:
17	chr1:168357609..168359334-chr1:168366941..168369901,2	K562	blood:
18	chr1:168380376..168383489-chr1:168385353..168387780,3	K562	blood:
19	chr1:168343623..168346188-chr1:168350297..168353036,3	K562	blood:
20	chr1:168348118..168353414-chr1:168355151..168359007,7	MCF-7	breast:
21	chr1:168380061..168382502-chr1:168391417..168394284,2	K562	blood:
22	chr1:168356981..168360579-chr1:168363528..168366891,3	MCF-7	breast:
23	chr1:168334562..168336538-chr1:168357801..168359534,2	K562	blood:
24	chr1:168368481..168370115-chr1:168372441..168374527,2	K562	blood:
25	chr1:168366951..168368452-chr1:168372047..168373905,2	K562	blood:
26	chr1:168356981..168360579-chr1:168363528..168366891,3	MCF-7	breast:
27	chr1:168187433..168189118-chr1:168341371..168344286,2	K562	blood:
28	chr1:168372698..168375484-chr1:168376700..168379733,3	K562	blood:
29	chr1:168342866..168344756-chr1:168372914..168374516,2	K562	blood:
30	chr1:168376462..168378908-chr20:55839505..55841906,2	MCF-7	breast:
31	chr1:168311615..168313900-chr1:168348090..168350975,2	MCF-7	breast:
32	chr1:168366951..168368657-chr1:168370802..168373547,2	K562	blood:
33	chr1:168366951..168368657-chr1:168370802..168373547,2	K562	blood:
34	chr1:168341145..168343864-chr1:168357058..168358969,2	K562	blood:
35	chr1:168346129..168348064-chr1:168353010..168355199,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XCL2-2	chr1:168382031-168382174	XLOC_001083
2	lnc-XCL2-2	chr1:168371277-168371581	XLOC_001083
3	lnc-XCL2-2	chr1:168370067-168371581	XLOC_001083
4	lnc-XCL2-2	chr1:168369427-168371581	NONHSAT007437
5	lnc-XCL2-2	chr1:168376477-168376512	XLOC_001083
6	lnc-XCL2-2	chr1:168370721-168370768	XLOC_001083
7	lnc-XCL2-2	chr1:168382031-168382174	NONHSAT007437

miRNA name	Chromosome Location	mirBase accession
hsa-miR-557	chr1:168344822-168344844	MIMAT0003221

No data

Variant related genes	Relation type
MIR557	TF binding region
ENSG00000228697	TF binding region
MIR557	CpG island
ENSG00000228697	CpG island
ENSG00000228697	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000226308	chromatin interactions
ENSG00000207974	chromatin interactions

Extended variants
information (count: 1481 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1481 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10753773	chr1:168343349-168343350	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs571792604	chr1:168343401-168343402	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs540024891	chr1:168343404-168343405	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs7549939	chr1:168343435-168343436	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs78732886	chr1:168343436-168343437	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs531539250	chr1:168343497-168343498	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs147956895	chr1:168343506-168343507	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs184931226	chr1:168343536-168343537	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs532352661	chr1:168343621-168343622	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs5778574	chr1:168343623-168343624	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs188818657	chr1:168343660-168343661	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs577251159	chr1:168343707-168343708	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs141574310	chr1:168343759-168343760	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs576408070	chr1:168343782-168343783	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs530216841	chr1:168343823-168343824	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs115615063	chr1:168343840-168343841	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs145341955	chr1:168343864-168343865	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs181452537	chr1:168343882-168343883	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs374251176	chr1:168343908-168343909	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs56086337	chr1:168343946-168343947	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs372785528	chr1:168343977-168343978	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs571019660	chr1:168344037-168344038	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs117600451	chr1:168344058-168344059	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs185994848	chr1:168344090-168344091	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs571855128	chr1:168344097-168344098	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs542303980	chr1:168344132-168344133	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs370119531	chr1:168344146-168344147	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs189279024	chr1:168344184-168344185	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs575656086	chr1:168344210-168344211	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs182027503	chr1:168344270-168344271	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs565218802	chr1:168344281-168344282	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs532286651	chr1:168344335-168344336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376619009	chr1:168344380-168344381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541269217	chr1:168344434-168344435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559581021	chr1:168344518-168344519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74123929	chr1:168344560-168344561	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs548703388	chr1:168344608-168344609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373381430	chr1:168344621-168344622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570134892	chr1:168344662-168344663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530947422	chr1:168344665-168344666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185760604	chr1:168344672-168344673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571151277	chr1:168344744-168344745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370414755	chr1:168344751-168344752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535003152	chr1:168344754-168344755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546829402	chr1:168344761-168344762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568324323	chr1:168344770-168344771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374126458	chr1:168344776-168344777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368301801	chr1:168344805-168344806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78825966	chr1:168344829-168344830	Enhancers Weak transcription	miRNA	n/a	Overlapped CNVs	n/a
50	rs374318773	chr1:168344830-168344831	Enhancers Weak transcription	miRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	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
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
Retinoblastoma	19183342	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
Chordoma	18071362	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
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	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
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:477 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168338200-168343400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:168338400-168348200	Weak transcription	HepG2	liver
3	chr1:168341800-168343400	Enhancers	Placenta Amnion	Placenta Amnion
4	chr1:168342000-168343400	Enhancers	Primary hematopoietic stem cells	blood
5	chr1:168342200-168343800	Weak transcription	Right Ventricle	heart
6	chr1:168342600-168343600	Weak transcription	Placenta	Placenta
7	chr1:168342600-168347400	Weak transcription	Right Atrium	heart
8	chr1:168342800-168345600	Enhancers	K562	blood
9	chr1:168343200-168343800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:168343600-168344800	Enhancers	Placenta	Placenta
11	chr1:168344400-168345600	Enhancers	Fetal Intestine Large	intestine
12	chr1:168344400-168345600	Enhancers	Fetal Intestine Small	intestine
13	chr1:168345600-168348000	Weak transcription	K562	blood
14	chr1:168346800-168347800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:168347000-168347800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:168348000-168349000	Enhancers	K562	blood
17	chr1:168348200-168348600	Enhancers	HepG2	liver
18	chr1:168348200-168349000	Enhancers	A549	lung
19	chr1:168348400-168348600	Enhancers	H9 Cell Line	embryonic stem cell
20	chr1:168348600-168354200	Weak transcription	HepG2	liver
21	chr1:168348600-168356600	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr1:168349400-168350800	Weak transcription	Aorta	Aorta
23	chr1:168350000-168356200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr1:168354200-168354800	Strong transcription	HepG2	liver
25	chr1:168354800-168367600	Weak transcription	HepG2	liver
26	chr1:168355200-168358800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr1:168355800-168356200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
28	chr1:168355800-168356400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr1:168355800-168357800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr1:168356000-168356200	Enhancers	Gastric	stomach
31	chr1:168356000-168356400	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr1:168356000-168356400	Enhancers	NHEK	skin
33	chr1:168356000-168356600	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr1:168356000-168357400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr1:168356000-168357400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr1:168356200-168356400	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr1:168356200-168356400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
38	chr1:168356200-168356400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr1:168356200-168356400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
40	chr1:168356200-168356400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr1:168356200-168356400	Enhancers	Ovary	ovary
42	chr1:168356200-168356600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr1:168356200-168356600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
44	chr1:168356200-168356600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr1:168356200-168356600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr1:168356200-168356600	Enhancers	Duodenum Mucosa	Duodenum
47	chr1:168356200-168356600	Enhancers	HMEC	breast
48	chr1:168356200-168356800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr1:168356200-168356800	Enhancers	Primary hematopoietic stem cells	blood
50	chr1:168356200-168356800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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