Variant report

Variant	nsv602903
Chromosome Location	chr6:34416388-34493012
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:948)
CpG islands
(count:1528)
Chromatin interactive
region (count:88)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:948 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34427137-34427322	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:34452906-34453066	K562	blood:	n/a	n/a
3	ARID3A	chr6:34485472-34485719	K562	blood:	n/a	n/a
4	ATF2	chr6:34427622-34428047	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr6:34458829-34459117	K562	blood:	n/a	n/a
6	ATF3	chr6:34433631-34433864	K562	blood:	n/a	n/a
7	ATF3	chr6:34452733-34453033	K562	blood:	n/a	n/a
8	ATF3	chr6:34485205-34485489	K562	blood:	n/a	n/a
9	BACH1	chr6:34458837-34459209	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr6:34418905-34419038	K562	blood:	n/a	n/a
11	BACH1	chr6:34458877-34459076	K562	blood:	n/a	n/a
12	BATF	chr6:34452746-34452975	GM12878	blood:	n/a	chr6:34452867-34452878
13	BCL3	chr6:34463889-34464156	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:34430406-34430445	K562	blood:	n/a	n/a
15	BHLHE40	chr6:34433443-34433930	K562	blood:	n/a	chr6:34433735-34433751
16	BHLHE40	chr6:34436208-34436550	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:34452706-34452850	K562	blood:	n/a	n/a
18	BHLHE40	chr6:34427751-34427973	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:34440239-34440572	K562	blood:	n/a	n/a
20	BHLHE40	chr6:34481627-34482576	K562	blood:	n/a	n/a
21	BHLHE40	chr6:34452753-34452980	GM12878	blood:	n/a	n/a
22	BHLHE40	chr6:34458903-34459141	K562	blood:	n/a	n/a
23	BRCA1	chr6:34458193-34458291	HepG2	liver:	n/a	n/a
24	BRCA1	chr6:34459183-34459214	HepG2	liver:	n/a	n/a
25	BRCA1	chr6:34434550-34434551	H1-hESC	embryonic stem cell:	n/a	n/a
26	CBX3	chr6:34485139-34485727	K562	blood:	n/a	n/a
27	CBX3	chr6:34427627-34428080	K562	blood:	n/a	n/a
28	CBX3	chr6:34486407-34486830	K562	blood:	n/a	n/a
29	CBX3	chr6:34425935-34426514	K562	blood:	n/a	n/a
30	CBX3	chr6:34458777-34459370	K562	blood:	n/a	n/a
31	CBX3	chr6:34441811-34442070	K562	blood:	n/a	n/a
32	CBX3	chr6:34461153-34461508	K562	blood:	n/a	n/a
33	CBX3	chr6:34467995-34468500	K562	blood:	n/a	n/a
34	CBX3	chr6:34441735-34442148	K562	blood:	n/a	n/a
35	CBX3	chr6:34433691-34434001	K562	blood:	n/a	n/a
36	CBX3	chr6:34486503-34486792	K562	blood:	n/a	n/a
37	CCNT2	chr6:34486987-34486989	K562	blood:	n/a	n/a
38	CCNT2	chr6:34433776-34434092	K562	blood:	n/a	n/a
39	CCNT2	chr6:34482363-34482613	K562	blood:	n/a	n/a
40	CEBPB	chr6:34457118-34457271	A549	lung:	n/a	chr6:34457182-34457193
41	CEBPB	chr6:34426323-34426556	IMR90	lung:	n/a	n/a
42	CEBPB	chr6:34426296-34426477	HepG2	liver:	n/a	n/a
43	CEBPB	chr6:34426242-34426591	HepG2	liver:	n/a	n/a
44	CEBPB	chr6:34426226-34426594	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:34441494-34441633	A549	lung:	n/a	n/a
46	CEBPB	chr6:34457122-34457295	Hela-S3	cervix:	n/a	chr6:34457182-34457193
47	CEBPB	chr6:34426275-34426523	K562	blood:	n/a	n/a
48	CEBPB	chr6:34419264-34419490	K562	blood:	n/a	n/a
49	CEBPB	chr6:34457041-34457338	K562	blood:	n/a	chr6:34457182-34457193
50	CEBPB	chr6:34457045-34457273	IMR90	lung:	n/a	chr6:34457182-34457193

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34433392-34433442	NH-A	brain:	n/a
2	chr6:34443983-34444033	HCF	heart:	n/a
3	chr6:34482411-34482461	BJ	skin:	n/a
4	chr6:34433392-34433442	NH-A	brain:	n/a
5	chr6:34443983-34444033	HCF	heart:	n/a
6	chr6:34482411-34482461	BJ	skin:	n/a
7	chr6:34433392-34433442	Jurkat	blood:	n/a
8	chr6:34434842-34434892	AoSMC	blood vessel:	n/a
9	chr6:34482479-34482529	NHBE	bronchial:	n/a
10	chr6:34433713-34433763	SAEC	small airway:	n/a
11	chr6:34464251-34464301	HRPEpiC	eye:	n/a
12	chr6:34434017-34434067	HRE	kidney:	n/a
13	chr6:34430625-34430675	NHDF-neo	bronchial:	n/a
14	chr6:34434076-34434126	BJ	skin:	n/a
15	chr6:34443983-34444033	GM19239	blood:	n/a
16	chr6:34433754-34433804	GM19239	blood:	n/a
17	chr6:34433392-34433442	A549	lung:	n/a
18	chr6:34482479-34482529	SK-N-SH_RA	brain:	n/a
19	chr6:34433392-34433442	AG09309	skin:	n/a
20	chr6:34433754-34433804	HepG2	liver:	n/a
21	chr6:34433320-34433370	GM12878	blood:	n/a
22	chr6:34486129-34486179	K562	blood:	n/a
23	chr6:34433676-34433726	SAEC	small airway:	n/a
24	chr6:34464251-34464301	AG04450	lung:	fetal
25	chr6:34434842-34434892	SAEC	small airway:	n/a
26	chr6:34492115-34492165	HUVEC	blood vessel:	n/a
27	chr6:34434017-34434067	GM06990	blood:	n/a
28	chr6:34434842-34434892	SK-N-SH	brain:	n/a
29	chr6:34482479-34482529	HCT-116	colon:	n/a
30	chr6:34433754-34433804	ovcar-3	ovarian:	n/a
31	chr6:34433676-34433726	HEEpiC	esophagus:	n/a
32	chr6:34492115-34492165	LNCaP	prostate:	n/a
33	chr6:34434017-34434067	A549	lung:	n/a
34	chr6:34464251-34464301	HepG2	liver:	n/a
35	chr6:34434325-34434375	AG09319	gingival:	n/a
36	chr6:34434017-34434067	HMEC	breast:	n/a
37	chr6:34434017-34434067	HNPCEpiC	eye:	n/a
38	chr6:34437227-34437277	MCF-7	breast:	n/a
39	chr6:34464251-34464301	K562	blood:	n/a
40	chr6:34434842-34434892	ECC-1	luminal epithelium:	n/a
41	chr6:34434325-34434375	HNPCEpiC	eye:	n/a
42	chr6:34437227-34437277	HNPCEpiC	eye:	n/a
43	chr6:34434017-34434067	K562	blood:	n/a
44	chr6:34433320-34433370	NT2-D1	testis:	n/a
45	chr6:34434842-34434892	HNPCEpiC	eye:	n/a
46	chr6:34489785-34489835	HNPCEpiC	eye:	n/a
47	chr6:34430625-34430675	AoSMC	blood vessel:	n/a
48	chr6:34430625-34430675	NHBE	bronchial:	n/a
49	chr6:34482411-34482461	SK-N-SH	brain:	n/a
50	chr6:34489785-34489835	PANC-1	pancreas:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:34454834..34457480-chr6:34459014..34462062,4	K562	blood:
2	chr6:34426062..34427951-chr6:34462962..34464594,2	K562	blood:
3	chr6:34430319..34432535-chr6:34490428..34492193,2	MCF-7	breast:
4	chr6:34419095..34420720-chr6:34421365..34423060,2	K562	blood:
5	chr6:34475212..34479816-chr6:34480006..34482829,5	K562	blood:
6	chr6:34435923..34437938-chr6:34439681..34442007,2	K562	blood:
7	chr6:34473007..34475169-chr6:34486448..34488656,2	K562	blood:
8	chr6:34430065..34432112-chr6:34462905..34465390,2	MCF-7	breast:
9	chr6:34431997..34433907-chr6:34759343..34761315,2	MCF-7	breast:
10	chr6:34441851..34443719-chr6:34445470..34448449,2	K562	blood:
11	chr6:34491195..34497458-chr6:34528901..34533837,5	K562	blood:
12	chr6:34439344..34441190-chr6:34462039..34464180,2	K562	blood:
13	chr6:34439690..34441668-chr6:34462680..34464330,2	K562	blood:
14	chr6:34479843..34482340-chr6:34557175..34560153,2	K562	blood:
15	chr6:34485669..34487625-chr6:34579770..34581445,2	K562	blood:
16	chr6:34454834..34457480-chr6:34459014..34462062,4	K562	blood:
17	chr6:34426062..34427951-chr6:34462962..34464594,2	K562	blood:
18	chr6:34484087..34487534-chr6:34488647..34495126,10	K562	blood:
19	chr6:34193853..34195785-chr6:34492922..34495154,2	K562	blood:
20	chr6:34441851..34443719-chr6:34445470..34448449,2	K562	blood:
21	chr6:34435923..34437938-chr6:34439681..34442007,2	K562	blood:
22	chr6:34490944..34493717-chr6:34499736..34502529,2	K562	blood:
23	chr6:34471689..34473248-chr6:34481488..34483012,2	K562	blood:
24	chr6:34430065..34432112-chr6:34462905..34465390,2	MCF-7	breast:
25	chr6:34419095..34420720-chr6:34421365..34423060,2	K562	blood:
26	chr6:34419123..34421664-chr6:34426882..34428491,2	K562	blood:
27	chr6:34390709..34393281-chr6:34426024..34429452,3	K562	blood:
28	chr6:34483206..34485571-chr6:34540552..34542756,2	K562	blood:
29	chr6:34450444..34452541-chr6:34453847..34456328,2	K562	blood:
30	chr6:34459450..34460981-chr6:34494263..34495839,2	K562	blood:
31	chr6:34450820..34454475-chr6:34457385..34459321,3	K562	blood:
32	chr6:34440695..34443428-chr6:34457495..34459339,2	MCF-7	breast:
33	chr6:34439344..34441190-chr6:34462039..34464180,2	K562	blood:
34	chr6:34491359..34493717-chr6:34499044..34502529,3	K562	blood:
35	chr6:34427418..34428084-chr6:34497140..34498209,3	MCF-7	breast:
36	chr6:34393131..34395376-chr6:34415836..34419033,3	K562	blood:
37	chr6:34467900..34469881-chr6:34479800..34481611,2	K562	blood:
38	chr6:34467900..34469881-chr6:34479800..34481611,2	K562	blood:
39	chr6:34427357..34428310-chr6:34577023..34577948,4	K562	blood:
40	chr6:34392344..34394131-chr6:34485515..34488152,2	MCF-7	breast:
41	chr6:34478801..34480566-chr6:34489552..34491373,2	K562	blood:
42	chr6:34473007..34475169-chr6:34486448..34488656,2	K562	blood:
43	chr6:34440695..34443428-chr6:34457495..34459339,2	MCF-7	breast:
44	chr6:34478801..34480566-chr6:34489552..34491373,2	K562	blood:
45	chr6:34486477..34488245-chr6:34492452..34495163,2	MCF-7	breast:
46	chr6:34421599..34423667-chr6:34425310..34428142,2	K562	blood:
47	chr6:34458604..34460671-chr6:34480867..34482983,2	K562	blood:
48	chr6:34432576..34434100-chr6:34439486..34441522,2	MCF-7	breast:
49	chr6:34427141..34428479-chr6:34576718..34577474,3	MCF-7	breast:
50	chr17:73388202..73390562-chr6:34449273..34451327,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000221635	TF binding region
PACSIN1	TF binding region
ENSG00000221635	CpG island
PACSIN1	CpG island
ENSG00000177885	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000272288	chromatin interactions
ENSG00000124507	chromatin interactions
ENSG00000065060	chromatin interactions
ENSG00000196821	chromatin interactions
ENSG00000186577	chromatin interactions
ENSG00000124614	chromatin interactions
ENSG00000265342	chromatin interactions

Extended variants
information (count: 3005 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:3005 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9394220	chr6:34416388-34416389	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536836394	chr6:34416395-34416396	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs555242719	chr6:34416416-34416417	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs148967314	chr6:34416429-34416430	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs116275391	chr6:34416432-34416433	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs182826252	chr6:34416434-34416435	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs34307089	chr6:34416441-34416442	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs67516707	chr6:34416454-34416455	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs56834165	chr6:34416473-34416474	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs565400407	chr6:34416479-34416480	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs185644420	chr6:34416490-34416491	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs11759152	chr6:34416504-34416505	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs113158702	chr6:34416517-34416518	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs376958218	chr6:34416519-34416520	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs183322374	chr6:34416582-34416583	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs531800684	chr6:34416613-34416614	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs550020147	chr6:34416676-34416677	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs565240630	chr6:34416690-34416691	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs35366933	chr6:34416714-34416715	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs532552088	chr6:34416734-34416735	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs547858371	chr6:34416746-34416747	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs370075666	chr6:34416750-34416751	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs528870681	chr6:34416751-34416752	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs566366739	chr6:34416760-34416761	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs374351935	chr6:34416847-34416848	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs536981082	chr6:34416873-34416874	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs548741884	chr6:34416877-34416878	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs4713791	chr6:34416893-34416894	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs57737848	chr6:34416907-34416908	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs111772372	chr6:34416939-34416940	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs375098528	chr6:34417000-34417001	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs148523971	chr6:34417021-34417022	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs372117278	chr6:34417045-34417046	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs193017832	chr6:34417178-34417179	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs534317994	chr6:34417221-34417222	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs552593253	chr6:34417233-34417234	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs574366025	chr6:34417242-34417243	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs112615810	chr6:34417257-34417258	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs111459735	chr6:34417297-34417298	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs186817277	chr6:34417304-34417305	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs78328123	chr6:34417333-34417334	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs570126427	chr6:34417342-34417343	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs532693178	chr6:34417348-34417349	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs541420522	chr6:34417349-34417350	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs566743585	chr6:34417380-34417381	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs577230580	chr6:34417417-34417418	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs530389987	chr6:34417419-34417420	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs12530115	chr6:34417441-34417442	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs570192981	chr6:34417467-34417468	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs531016547	chr6:34417477-34417478	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1108 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34394400-34433200	Weak transcription	Right Atrium	heart
2	chr6:34415000-34417800	Enhancers	Fetal Brain Male	brain
3	chr6:34415400-34417200	Enhancers	Fetal Brain Female	brain
4	chr6:34415400-34417800	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr6:34415600-34416400	Enhancers	H1 Cell Line	embryonic stem cell
6	chr6:34415600-34424600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:34415800-34416800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:34415800-34417000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr6:34416000-34416400	Flanking Active TSS	Placenta	Placenta
10	chr6:34416000-34416800	Weak transcription	K562	blood
11	chr6:34416200-34416600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr6:34416200-34416600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:34416200-34416600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:34416400-34418000	Enhancers	Placenta	Placenta
15	chr6:34416600-34417200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr6:34416600-34417400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr6:34416600-34417400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:34416800-34417000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr6:34416800-34417200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:34416800-34417200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr6:34416800-34417400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:34417000-34417600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr6:34417600-34428000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr6:34418600-34418800	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr6:34418600-34418800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr6:34419200-34419600	Active TSS	Fetal Heart	heart
27	chr6:34422800-34423000	Enhancers	H1 Cell Line	embryonic stem cell
28	chr6:34423800-34425400	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr6:34424200-34425600	Enhancers	Fetal Thymus	thymus
30	chr6:34424600-34424800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr6:34424600-34424800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr6:34424600-34424800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr6:34424600-34425200	Bivalent Enhancer	HepG2	liver
34	chr6:34424600-34426400	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr6:34424600-34426600	Enhancers	K562	blood
36	chr6:34424800-34425000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:34424800-34425000	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr6:34424800-34425200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr6:34424800-34425200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr6:34424800-34425600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr6:34425000-34425200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr6:34425000-34425600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr6:34425000-34425800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr6:34425000-34429000	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr6:34425200-34425400	Flanking Bivalent TSS/Enh	HepG2	liver
46	chr6:34425200-34425600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:34425200-34426000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:34425200-34426000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr6:34425200-34426600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr6:34425400-34425600	Flanking Active TSS	HepG2	liver

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