Variant report

Variant	nsv548055
Chromosome Location	chr1:159918418-159940000
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:159)
CpG islands
(count:489)
Chromatin interactive
region (count:26)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:159 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:159934747-159934786	K562	blood:	n/a	n/a
2	ARID3A	chr1:159927422-159927876	K562	blood:	n/a	n/a
3	ATF1	chr1:159923940-159924205	K562	blood:	n/a	n/a
4	ATF1	chr1:159930887-159931113	K562	blood:	n/a	n/a
5	ATF1	chr1:159927611-159928120	K562	blood:	n/a	n/a
6	ATF2	chr1:159928474-159928886	GM12878	blood:	n/a	n/a
7	BATF	chr1:159928452-159929056	GM12878	blood:	n/a	n/a
8	BATF	chr1:159928491-159928876	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:159923808-159923890	K562	blood:	n/a	n/a
10	BHLHE40	chr1:159918876-159918999	K562	blood:	n/a	n/a
11	BHLHE40	chr1:159927651-159928083	K562	blood:	n/a	n/a
12	CCNT2	chr1:159927634-159928259	K562	blood:	n/a	n/a
13	CEBPB	chr1:159930867-159931186	K562	blood:	n/a	chr1:159930982-159930990
14	CEBPB	chr1:159930576-159931175	IMR90	lung:	n/a	chr1:159930982-159930990
15	CEBPB	chr1:159930842-159931171	Hela-S3	cervix:	n/a	chr1:159930982-159930990
16	CEBPD	chr1:159927467-159927887	K562	blood:	n/a	n/a
17	CEBPD	chr1:159927455-159927975	K562	blood:	n/a	n/a
18	CTCF	chr1:159923044-159923074	GM20000	blood:	n/a	n/a
19	CTCF	chr1:159927662-159927731	K562	blood:	n/a	n/a
20	CTCF	chr1:159927880-159928030	SAEC	small airway:	n/a	n/a
21	CTCF	chr1:159928012-159928081	Pancreas_OC	pancreas:	n/a	n/a
22	CTCF	chr1:159927982-159928062	LNCaP	prostate:	n/a	n/a
23	CTCF	chr1:159927940-159928090	NHEK	skin:	n/a	n/a
24	CUX1	chr1:159930716-159930845	K562	blood:	n/a	n/a
25	ELF1	chr1:159927672-159927830	K562	blood:	n/a	n/a
26	EP300	chr1:159927750-159928248	T-47D	breast:	n/a	n/a
27	EP300	chr1:159927675-159928282	ECC-1	luminal epithelium:	n/a	n/a
28	EP300	chr1:159927770-159928185	T-47D	breast:	n/a	n/a
29	EP300	chr1:159924189-159924556	K562	blood:	n/a	chr1:159924404-159924418
30	EP300	chr1:159927514-159928183	K562	blood:	n/a	chr1:159927607-159927621
31	EP300	chr1:159918906-159918950	K562	blood:	n/a	n/a
32	EP300	chr1:159918746-159919505	ECC-1	luminal epithelium:	n/a	chr1:159918863-159918872 chr1:159919435-159919445
33	FAM48A	chr1:159930891-159931046	GM12878	blood:	n/a	n/a
34	FOS	chr1:159929360-159929540	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr1:159930369-159931123	MCF10A-Er-Src	breast:	n/a	chr1:159930983-159930992
36	FOS	chr1:159930386-159931090	MCF10A-Er-Src	breast:	n/a	chr1:159930983-159930992
37	FOS	chr1:159932941-159933093	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr1:159930362-159931187	MCF10A-Er-Src	breast:	n/a	chr1:159930983-159930992
39	FOS	chr1:159923994-159924234	MCF10A-Er-Src	breast:	n/a	chr1:159924165-159924173 chr1:159924163-159924174
40	FOS	chr1:159925447-159925494	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr1:159932923-159933009	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr1:159923923-159924324	MCF10A-Er-Src	breast:	n/a	chr1:159924165-159924173 chr1:159924163-159924174
43	FOS	chr1:159930399-159931180	MCF10A-Er-Src	breast:	n/a	chr1:159930983-159930992
44	FOS	chr1:159919062-159919210	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr1:159924026-159924146	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr1:159923925-159924350	MCF10A-Er-Src	breast:	n/a	chr1:159924165-159924173 chr1:159924163-159924174
47	FOXA1	chr1:159927828-159928147	T-47D	breast:	n/a	chr1:159928020-159928035
48	FOXA1	chr1:159927777-159928165	T-47D	breast:	n/a	chr1:159928020-159928035
49	FOXA1	chr1:159927852-159928150	ECC-1	luminal epithelium:	n/a	chr1:159928020-159928035
50	FOXA1	chr1:159927824-159928092	ECC-1	luminal epithelium:	n/a	chr1:159928020-159928035

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:159923861-159923911	LNCaP	prostate:	n/a
2	chr1:159923861-159923911	LNCaP	prostate:	n/a
3	chr1:159925416-159925466	ovcar-3	ovarian:	n/a
4	chr1:159924541-159924591	MCF10A-Er-Src	breast:	n/a
5	chr1:159924541-159924591	ovcar-3	ovarian:	n/a
6	chr1:159924541-159924591	HCF	heart:	n/a
7	chr1:159921548-159921598	SKMC	muscle:	n/a
8	chr1:159923525-159923575	HUVEC	blood vessel:	n/a
9	chr1:159923861-159923911	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:159924541-159924591	HRPEpiC	eye:	n/a
11	chr1:159923861-159923911	HCF	heart:	n/a
12	chr1:159925272-159925322	Hela-S3	cervix:	n/a
13	chr1:159919350-159919400	K562	blood:	n/a
14	chr1:159923725-159923775	HNPCEpiC	eye:	n/a
15	chr1:159925272-159925322	SK-N-SH	brain:	n/a
16	chr1:159923725-159923775	HRPEpiC	eye:	n/a
17	chr1:159919350-159919400	A549	lung:	n/a
18	chr1:159919350-159919400	AoSMC	blood vessel:	n/a
19	chr1:159923525-159923575	Hela-S3	cervix:	n/a
20	chr1:159923861-159923911	SK-N-SH_RA	brain:	n/a
21	chr1:159923525-159923575	Caco-2	colon:	n/a
22	chr1:159925416-159925466	Hepatocyte	liver:	n/a
23	chr1:159919350-159919400	HCF	heart:	n/a
24	chr1:159923525-159923575	HEEpiC	esophagus:	n/a
25	chr1:159925416-159925466	HCF	heart:	n/a
26	chr1:159924541-159924591	HCPEpiC	choroid plexus:	n/a
27	chr1:159923725-159923775	GM06990	blood:	n/a
28	chr1:159919350-159919400	RPTEC	kidney:	n/a
29	chr1:159925272-159925322	GM12878	blood:	n/a
30	chr1:159924541-159924591	Hela-S3	cervix:	n/a
31	chr1:159923525-159923575	ProgFib	skin:	n/a
32	chr1:159923525-159923575	NH-A	brain:	n/a
33	chr1:159923861-159923911	SK-N-MC	brain:	n/a
34	chr1:159925272-159925322	AG04449	skin:	fetal
35	chr1:159921548-159921598	NHBE	bronchial:	n/a
36	chr1:159923525-159923575	ECC-1	luminal epithelium:	n/a
37	chr1:159925416-159925466	AG09319	gingival:	n/a
38	chr1:159923725-159923775	SK-N-MC	brain:	n/a
39	chr1:159925416-159925466	BE2_C	brain:	n/a
40	chr1:159919350-159919400	HAEpiC	amniotic membrane:	n/a
41	chr1:159919350-159919400	SKMC	muscle:	n/a
42	chr1:159923725-159923775	HMEC	breast:	n/a
43	chr1:159925272-159925322	HCF	heart:	n/a
44	chr1:159923725-159923775	BJ	skin:	n/a
45	chr1:159921548-159921598	HEK293	kidney:	embryo
46	chr1:159925416-159925466	MCF-7	breast:	n/a
47	chr1:159919350-159919400	HMEC	breast:	n/a
48	chr1:159924541-159924591	AG04449	skin:	fetal
49	chr1:159925272-159925322	BE2_C	brain:	n/a
50	chr1:159923525-159923575	AG10803	skin:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:159913231..159916078-chr1:159934626..159937390,2	MCF-7	breast:
2	chr1:159893768..159896638-chr1:159931610..159934083,3	K562	blood:
3	chr1:159922806..159924393-chr1:159927902..159929423,2	MCF-7	breast:
4	chr1:159926244..159929298-chr1:159931208..159934136,4	K562	blood:
5	chr1:159889594..159891125-chr1:159920151..159921764,2	K562	blood:
6	chr1:159915177..159916048-chr1:159924751..159925565,2	K562	blood:
7	chr1:159914809..159917137-chr1:159930388..159932667,2	K562	blood:
8	chr1:159892760..159896965-chr1:159922291..159925141,4	K562	blood:
9	chr1:159894586..159896290-chr1:159926599..159929253,2	K562	blood:
10	chr1:159914406..159916851-chr1:159926521..159929440,2	MCF-7	breast:
11	chr1:159915479..159916369-chr1:159939426..159941106,4	MCF-7	breast:
12	chr1:159906196..159907844-chr1:159918689..159920496,2	K562	blood:
13	chr1:159893947..159895991-chr1:159928260..159930233,2	MCF-7	breast:
14	chr1:159914087..159917108-chr1:159918737..159921842,4	K562	blood:
15	chr1:159914087..159917406-chr1:159919502..159922854,5	K562	blood:
16	chr1:159925103..159927154-chr1:159928753..159930871,2	MCF-7	breast:
17	chr1:159914982..159917172-chr1:159939218..159941939,2	K562	blood:
18	chr1:159905137..159907886-chr1:159939775..159941971,2	MCF-7	breast:
19	chr1:159925103..159927154-chr1:159928753..159930871,2	MCF-7	breast:
20	chr1:159913973..159917644-chr1:159927852..159934070,11	MCF-7	breast:
21	chr1:159907782..159910427-chr1:159933319..159935593,2	MCF-7	breast:
22	chr1:159907235..159909524-chr1:159933511..159935771,2	MCF-7	breast:
23	chr1:159921624..159923917-chr1:159925948..159927812,2	K562	blood:
24	chr1:159912050..159914185-chr1:159918859..159921422,2	MCF-7	breast:
25	chr1:159926244..159929298-chr1:159931208..159934136,4	K562	blood:
26	chr1:159934579..159937237-chr1:159944112..159946274,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNJ9-2	chr1:159930965-159931195	NONHSAT007031
2	lnc-KCNJ9-2	chr1:159935289-159935435	NONHSAT007031
3	lnc-KCNJ9-2	chr1:159931014-159931195	NONHSAT007033
4	lnc-KCNJ9-2	chr1:159931008-159931195	ENSG00000224259
5	lnc-KCNJ9-2	chr1:159935289-159935435	ENSG00000224259
6	lnc-KCNJ9-2	chr1:159931014-159931195	ENSG00000224259

No data

Variant related genes	Relation type
SLAMF9	TF binding region
LINC01133	TF binding region
IGSF9	TF binding region
SLAMF9	CpG island
LINC01133	CpG island
IGSF9	CpG island
ENSG00000085552	chromatin interactions
ENSG00000162723	chromatin interactions
ENSG00000158710	chromatin interactions

Extended variants
information (count: 839 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:839 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4656248	chr1:159918418-159918419	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554100668	chr1:159918420-159918421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149978774	chr1:159918564-159918565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541765777	chr1:159918602-159918603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141286445	chr1:159918623-159918624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112151044	chr1:159918661-159918662	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs144253613	chr1:159918701-159918702	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs141016344	chr1:159918743-159918744	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs550705543	chr1:159918750-159918751	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs543171001	chr1:159918775-159918776	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs374836906	chr1:159918783-159918784	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs561634747	chr1:159918825-159918826	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs528956894	chr1:159918833-159918834	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs34128710	chr1:159918871-159918872	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs112384015	chr1:159919005-159919006	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs565705778	chr1:159919090-159919091	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs183405648	chr1:159919110-159919111	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs547302667	chr1:159919119-159919120	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs552952300	chr1:159919126-159919127	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs564289547	chr1:159919216-159919217	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs571152184	chr1:159919243-159919244	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs532014570	chr1:159919273-159919274	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs538451034	chr1:159919307-159919308	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs556765312	chr1:159919311-159919312	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs189159179	chr1:159919347-159919348	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs371676545	chr1:159919350-159919351	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs553952193	chr1:159919362-159919363	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs144926819	chr1:159919366-159919367	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs147921600	chr1:159919408-159919409	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs71628158	chr1:159919448-159919449	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs34508581	chr1:159919625-159919626	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs375328746	chr1:159919664-159919665	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs141776518	chr1:159919682-159919683	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs561888836	chr1:159919718-159919719	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529065408	chr1:159919757-159919758	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs541151883	chr1:159919768-159919769	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs35494843	chr1:159919781-159919782	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs142939336	chr1:159919794-159919795	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs532999605	chr1:159919835-159919836	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs533473189	chr1:159919842-159919843	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs551357029	chr1:159919852-159919853	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs549860163	chr1:159919957-159919958	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs192465777	chr1:159919960-159919961	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532006812	chr1:159919970-159919971	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs2820579	chr1:159919986-159919987	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs568665792	chr1:159920063-159920064	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs150954106	chr1:159920076-159920077	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs542805695	chr1:159920122-159920123	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs376575702	chr1:159920123-159920124	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs554278746	chr1:159920187-159920188	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	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
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	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
Bladder cancer	21909424	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	19602461	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:159915800-159919600	Weak transcription	Lung	lung
2	chr1:159916000-159918800	Weak transcription	Colon Smooth Muscle	Colon
3	chr1:159916200-159918800	Weak transcription	K562	blood
4	chr1:159916200-159919000	Weak transcription	A549	lung
5	chr1:159916200-159919800	Enhancers	Fetal Intestine Small	intestine
6	chr1:159916200-159920000	Enhancers	Stomach Mucosa	stomach
7	chr1:159916200-159930600	Weak transcription	Right Atrium	heart
8	chr1:159916600-159918600	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr1:159916600-159918800	Weak transcription	Placenta	Placenta
10	chr1:159916600-159919600	Weak transcription	Colonic Mucosa	Colon
11	chr1:159916600-159920800	Weak transcription	Fetal Lung	lung
12	chr1:159916800-159918600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr1:159916800-159918800	Weak transcription	Esophagus	oesophagus
14	chr1:159916800-159918800	Weak transcription	Fetal Kidney	kidney
15	chr1:159916800-159918800	Weak transcription	Pancreas	Pancrea
16	chr1:159916800-159919000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr1:159916800-159919000	Weak transcription	Gastric	stomach
18	chr1:159916800-159919200	Weak transcription	HMEC	breast
19	chr1:159916800-159923600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:159917000-159918600	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr1:159917000-159918800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr1:159917000-159919800	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr1:159917000-159923400	Weak transcription	NHEK	skin
24	chr1:159917600-159919800	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr1:159918000-159919800	Enhancers	Duodenum Mucosa	Duodenum
26	chr1:159918200-159919800	Enhancers	Fetal Intestine Large	intestine
27	chr1:159918400-159918600	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr1:159918600-159920000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr1:159918600-159920000	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr1:159918600-159920400	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr1:159918600-159921400	Enhancers	Placenta Amnion	Placenta Amnion
32	chr1:159918800-159919000	Enhancers	Rectal Smooth Muscle	rectum
33	chr1:159918800-159919200	Enhancers	Fetal Kidney	kidney
34	chr1:159918800-159919400	Enhancers	Placenta	Placenta
35	chr1:159918800-159919400	Enhancers	K562	blood
36	chr1:159918800-159919600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr1:159918800-159919600	Enhancers	Colon Smooth Muscle	Colon
38	chr1:159918800-159919600	Enhancers	Pancreas	Pancrea
39	chr1:159918800-159919800	Enhancers	Esophagus	oesophagus
40	chr1:159919000-159919200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr1:159919000-159919200	Enhancers	Gastric	stomach
42	chr1:159919000-159919600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr1:159919000-159920000	Enhancers	Fetal Stomach	stomach
44	chr1:159919200-159919400	Enhancers	A549	lung
45	chr1:159919200-159919400	Enhancers	HMEC	breast
46	chr1:159919200-159919800	Weak transcription	Gastric	stomach
47	chr1:159919200-159920200	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr1:159919400-159923600	Weak transcription	K562	blood
49	chr1:159919600-159919800	Enhancers	Lung	lung
50	chr1:159919600-159920400	Enhancers	Colonic Mucosa	Colon

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