Variant report

Variant	esv1807546
Chromosome Location	chr6:26378681-26387546
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:320)
CpG islands
(count:429)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:320 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:26383245-26383472	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:26379721-26379968	K562	blood:	n/a	n/a
3	ATF1	chr6:26379681-26379920	K562	blood:	n/a	n/a
4	ATF1	chr6:26383091-26383465	K562	blood:	n/a	n/a
5	ATF1	chr6:26384288-26384605	K562	blood:	n/a	n/a
6	ATF3	chr6:26384220-26384567	K562	blood:	n/a	n/a
7	BHLHE40	chr6:26385594-26385771	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:26383051-26383475	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:26383196-26383520	HepG2	liver:	n/a	n/a
10	BHLHE40	chr6:26383124-26383727	K562	blood:	n/a	n/a
11	BRCA1	chr6:26383338-26383539	GM12878	blood:	n/a	n/a
12	BRCA1	chr6:26383156-26383464	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr6:26383245-26383595	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr6:26383197-26383433	HepG2	liver:	n/a	n/a
15	CBX3	chr6:26383574-26384637	K562	blood:	n/a	chr6:26384271-26384282
16	CCNT2	chr6:26384407-26384584	K562	blood:	n/a	n/a
17	CCNT2	chr6:26379819-26379837	K562	blood:	n/a	n/a
18	CHD2	chr6:26383224-26383527	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr6:26383162-26383580	K562	blood:	n/a	n/a
20	CHD2	chr6:26383160-26383790	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr6:26383141-26383567	GM12878	blood:	n/a	n/a
22	CHD2	chr6:26383203-26383751	HepG2	liver:	n/a	n/a
23	CREB1	chr6:26383016-26383672	GM12878	blood:	n/a	n/a
24	CREB1	chr6:26382960-26383680	HepG2	liver:	n/a	n/a
25	CREB1	chr6:26383166-26383441	A549	lung:	n/a	n/a
26	CREB1	chr6:26383014-26383637	GM12878	blood:	n/a	n/a
27	CREB1	chr6:26383064-26383626	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr6:26383168-26383457	A549	lung:	n/a	n/a
29	CREB1	chr6:26383026-26383504	ECC-1	luminal epithelium:	n/a	n/a
30	CREB1	chr6:26382847-26383718	K562	blood:	n/a	n/a
31	CREB1	chr6:26383137-26383493	ECC-1	luminal epithelium:	n/a	n/a
32	CREB1	chr6:26383016-26383600	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr6:26382961-26383624	HepG2	liver:	n/a	n/a
34	CTCF	chr6:26383460-26383610	AG04449	skin:	n/a	n/a
35	CTCF	chr6:26383640-26383790	GM12864	blood:	n/a	n/a
36	CTCF	chr6:26383540-26383690	HMEC	breast:	n/a	n/a
37	CTCF	chr6:26383500-26383650	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr6:26383520-26383670	GM12872	blood:	n/a	n/a
39	CTCF	chr6:26383520-26383670	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr6:26383508-26383720	GM12878	blood:	n/a	n/a
41	CTCF	chr6:26383540-26383690	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr6:26383560-26383710	AG10803	skin:	n/a	n/a
43	CTCF	chr6:26383489-26383634	GM19240	blood:	n/a	n/a
44	CTCF	chr6:26383900-26384050	GM12873	blood:	n/a	n/a
45	CTCF	chr6:26383580-26383730	RPTEC	kidney:	n/a	n/a
46	CTCF	chr6:26383520-26383670	GM12875	blood:	n/a	n/a
47	CTCF	chr6:26383540-26383690	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr6:26383360-26383510	Caco-2	colon:	n/a	n/a
49	CTCF	chr6:26383500-26383650	AG09319	gingival:	n/a	n/a
50	CTCF	chr6:26383600-26383750	NHEK	skin:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26383673-26383723	PFSK-1	brain:	n/a
2	chr6:26383673-26383723	Jurkat	blood:	n/a
3	chr6:26383673-26383723	PFSK-1	brain:	n/a
4	chr6:26383673-26383723	Jurkat	blood:	n/a
5	chr6:26383374-26383424	HNPCEpiC	eye:	n/a
6	chr6:26383297-26383347	Caco-2	colon:	n/a
7	chr6:26382695-26382745	NB4	blood:	n/a
8	chr6:26383297-26383347	HNPCEpiC	eye:	n/a
9	chr6:26383297-26383347	NH-A	brain:	n/a
10	chr6:26383004-26383054	AG09319	gingival:	n/a
11	chr6:26383004-26383054	HUVEC	blood vessel:	n/a
12	chr6:26383297-26383347	BJ	skin:	n/a
13	chr6:26383297-26383347	LNCaP	prostate:	n/a
14	chr6:26386191-26386241	HUVEC	blood vessel:	n/a
15	chr6:26383374-26383424	NHBE	bronchial:	n/a
16	chr6:26383004-26383054	HCT-116	colon:	n/a
17	chr6:26382695-26382745	GM12878	blood:	n/a
18	chr6:26383297-26383347	RPTEC	kidney:	n/a
19	chr6:26386191-26386241	HRE	kidney:	n/a
20	chr6:26383374-26383424	NB4	blood:	n/a
21	chr6:26383374-26383424	SK-N-SH_RA	brain:	n/a
22	chr6:26383374-26383424	GM12892	blood:	n/a
23	chr6:26383297-26383347	SK-N-SH	brain:	n/a
24	chr6:26383673-26383723	NB4	blood:	n/a
25	chr6:26383374-26383424	HUVEC	blood vessel:	n/a
26	chr6:26383004-26383054	NB4	blood:	n/a
27	chr6:26386191-26386241	HMEC	breast:	n/a
28	chr6:26382695-26382745	HCM	heart:	n/a
29	chr6:26383004-26383054	RPTEC	kidney:	n/a
30	chr6:26383673-26383723	HIPEpiC	eye:	n/a
31	chr6:26383297-26383347	AG09319	gingival:	n/a
32	chr6:26386191-26386241	GM12878	blood:	n/a
33	chr6:26382817-26382867	HL-60	blood:	n/a
34	chr6:26383004-26383054	SK-N-MC	brain:	n/a
35	chr6:26382695-26382745	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:26383004-26383054	K562	blood:	n/a
37	chr6:26383673-26383723	HCM	heart:	n/a
38	chr6:26383297-26383347	NHBE	bronchial:	n/a
39	chr6:26383297-26383347	HCF	heart:	n/a
40	chr6:26383374-26383424	PANC-1	pancreas:	n/a
41	chr6:26383297-26383347	AG09309	skin:	n/a
42	chr6:26383673-26383723	K562	blood:	n/a
43	chr6:26382817-26382867	HRCEpiC	kidney:	n/a
44	chr6:26382817-26382867	ovcar-3	ovarian:	n/a
45	chr6:26383297-26383347	HAEpiC	amniotic membrane:	n/a
46	chr6:26383297-26383347	HL-60	blood:	n/a
47	chr6:26383673-26383723	U87	brain:	n/a
48	chr6:26383297-26383347	ProgFib	skin:	n/a
49	chr6:26383297-26383347	HRPEpiC	eye:	n/a
50	chr6:26383297-26383347	CMK	blood:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26378930..26384775-chr6:26385231..26390850,8	MCF-7	breast:
2	chr6:26376258..26380187-chr6:26381333..26383262,3	K562	blood:
3	chr6:26188276..26190980-chr6:26381179..26383865,2	K562	blood:
4	chr6:26384661..26390027-chr6:26390440..26394308,9	K562	blood:
5	chr6:26373111..26374832-chr6:26379026..26381530,2	MCF-7	breast:
6	chr6:26376258..26380187-chr6:26381333..26383262,3	K562	blood:
7	chr6:26363140..26366680-chr6:26382117..26385194,3	MCF-7	breast:
8	chr6:26370389..26374393-chr6:26375542..26380304,5	K562	blood:
9	chr6:26378930..26384775-chr6:26385231..26390850,8	MCF-7	breast:
10	chr6:26056232..26057928-chr6:26382432..26384674,2	K562	blood:
11	chr6:26365252..26366783-chr6:26384022..26386049,2	K562	blood:
12	chr6:26197076..26199216-chr6:26383709..26386156,2	K562	blood:
13	chr6:26381514..26383162-chr6:26388270..26390930,2	K562	blood:
14	chr6:26384982..26386521-chr6:26418535..26421413,2	K562	blood:
15	chr6:26385648..26389626-chr6:26390686..26394827,7	K562	blood:
16	chr6:26386609..26388143-chr6:26388160..26389725,2	K562	blood:
17	chr6:26373307..26375855-chr6:26376435..26379484,4	K562	blood:
18	chr6:26380688..26382359-chr6:26523846..26526048,2	K562	blood:
19	chr6:26385663..26388143-chr6:26388160..26389788,2	K562	blood:
20	chr6:26373194..26374949-chr6:26387423..26389905,2	K562	blood:
21	chr6:26231864..26233958-chr6:26385034..26386589,2	K562	blood:
22	chr6:26374643..26376462-chr6:26381050..26382858,2	K562	blood:
23	chr6:26365183..26366783-chr6:26383299..26386049,2	K562	blood:
24	chr6:26384219..26387977-chr6:26401180..26404441,3	K562	blood:
25	chr6:26378690..26380275-chr6:26532676..26534577,2	K562	blood:
26	chr6:26350980..26353776-chr6:26378882..26380453,2	K562	blood:
27	chr6:26386249..26387977-chr6:26410768..26413470,2	K562	blood:
28	chr6:26386746..26389506-chr6:27100599..27103516,2	K562	blood:
29	chr6:26383587..26385903-chr6:26419597..26421640,2	MCF-7	breast:
30	chr6:26381677..26383433-chr6:26537712..26539518,2	K562	blood:
31	chr6:26384869..26386538-chr6:26388093..26389767,2	MCF-7	breast:
32	chr6:26383299..26384986-chr6:26520070..26522600,2	K562	blood:
33	chr6:26382632..26385246-chr6:26444412..26446084,2	K562	blood:

No data

Variant related genes	Relation type
BTN2A2	TF binding region
BTN2A2	CpG island
ENSG00000228223	chromatin interactions
ENSG00000186470	chromatin interactions
ENSG00000218281	chromatin interactions
ENSG00000026950	chromatin interactions
ENSG00000215979	chromatin interactions
ENSG00000124508	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000188987	chromatin interactions
ENSG00000197409	chromatin interactions
ENSG00000182952	chromatin interactions
ENSG00000187837	chromatin interactions
ENSG00000111801	chromatin interactions
ENSG00000124549	chromatin interactions
ENSG00000252399	chromatin interactions

Extended variants
information (count: 374 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:374 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1624064	chr6:26378681-26378682	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
2	rs556140058	chr6:26378782-26378783	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs138082540	chr6:26378800-26378801	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs117310425	chr6:26378833-26378834	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs555578580	chr6:26378838-26378839	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs72841540	chr6:26378857-26378858	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs191422267	chr6:26378879-26378880	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs530846346	chr6:26378896-26378897	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs560355729	chr6:26378907-26378908	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs184602283	chr6:26378925-26378926	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs546074349	chr6:26378992-26378993	Enhancers Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs570840385	chr6:26379075-26379076	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs145631793	chr6:26379076-26379077	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs562477766	chr6:26379091-26379092	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs531204698	chr6:26379116-26379117	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs190314099	chr6:26379131-26379132	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs114731331	chr6:26379146-26379147	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs182444334	chr6:26379151-26379152	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs9467728	chr6:26379196-26379197	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs535692102	chr6:26379244-26379245	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs570661964	chr6:26379295-26379296	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs9467729	chr6:26379298-26379299	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs550053712	chr6:26379302-26379303	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs9467730	chr6:26379309-26379310	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs113435302	chr6:26379346-26379347	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs555868063	chr6:26379350-26379351	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs9467731	chr6:26379358-26379359	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs535093307	chr6:26379404-26379405	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs113260247	chr6:26379413-26379414	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs374012097	chr6:26379414-26379415	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs185047797	chr6:26379438-26379439	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs9467732	chr6:26379440-26379441	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs367581340	chr6:26379463-26379464	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs546164161	chr6:26379480-26379481	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs556162052	chr6:26379517-26379518	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs188939043	chr6:26379523-26379524	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs541476773	chr6:26379532-26379533	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs386698233	chr6:26379537-26379538	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs569442616	chr6:26379538-26379539	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs181053936	chr6:26379539-26379540	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs185432928	chr6:26379540-26379541	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs527395790	chr6:26379545-26379546	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs375548145	chr6:26379546-26379547	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs190285731	chr6:26379552-26379553	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs180781058	chr6:26379583-26379584	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs116855140	chr6:26379606-26379607	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs534560738	chr6:26379637-26379638	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs186150011	chr6:26379638-26379639	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs145897527	chr6:26379640-26379641	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs9467733	chr6:26379675-26379676	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Williams-beuren syndrome	16971481	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Autism	22495309	CNVD
Lung cancer	21569311	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26366000-26382600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr6:26366000-26383000	Weak transcription	Brain Hippocampus Middle	brain
3	chr6:26366000-26383200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr6:26366000-26383200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr6:26366000-26383200	Weak transcription	Pancreas	Pancrea
6	chr6:26366000-26383200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr6:26366000-26383200	Weak transcription	HSMMtube	muscle
8	chr6:26366000-26383400	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr6:26366200-26382400	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr6:26366200-26383200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr6:26366200-26383200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr6:26367000-26383000	Weak transcription	NHEK	skin
13	chr6:26367000-26383200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr6:26369800-26383000	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr6:26370400-26383000	Weak transcription	Brain Cingulate Gyrus	brain
16	chr6:26370800-26379000	Strong transcription	Primary T cells from cord blood	blood
17	chr6:26370800-26383200	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr6:26371000-26383200	Weak transcription	Right Ventricle	heart
19	chr6:26374000-26382400	Weak transcription	Dnd41	blood
20	chr6:26375200-26383200	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr6:26375200-26383200	Weak transcription	Colon Smooth Muscle	Colon
22	chr6:26375200-26383200	Weak transcription	Fetal Lung	lung
23	chr6:26375200-26383200	Weak transcription	Osteobl	bone
24	chr6:26375400-26383000	Weak transcription	Rectal Smooth Muscle	rectum
25	chr6:26375600-26383200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr6:26375600-26383200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr6:26375800-26381400	Weak transcription	HepG2	liver
28	chr6:26375800-26382800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr6:26375800-26383000	Weak transcription	Brain Anterior Caudate	brain
30	chr6:26375800-26383000	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr6:26375800-26383000	Weak transcription	Stomach Mucosa	stomach
32	chr6:26375800-26383200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr6:26375800-26383200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr6:26375800-26383200	Weak transcription	Placenta	Placenta
35	chr6:26375800-26383200	Weak transcription	Hela-S3	cervix
36	chr6:26376000-26381200	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr6:26376000-26383000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr6:26376000-26383200	Weak transcription	Esophagus	oesophagus
39	chr6:26376000-26383200	Weak transcription	Ovary	ovary
40	chr6:26376000-26383400	Weak transcription	Gastric	stomach
41	chr6:26376200-26381200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr6:26376200-26382400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr6:26376200-26383000	Weak transcription	Stomach Smooth Muscle	stomach
44	chr6:26376200-26383200	Weak transcription	Fetal Muscle Trunk	muscle
45	chr6:26376200-26383200	Weak transcription	Left Ventricle	heart
46	chr6:26377000-26383000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr6:26377000-26383000	Weak transcription	Adipose Nuclei	Adipose
48	chr6:26377000-26383200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr6:26377000-26383200	Weak transcription	Aorta	Aorta
50	chr6:26377000-26383200	Weak transcription	Colonic Mucosa	Colon

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