Variant report

Variant	esv1801907
Chromosome Location	chr6:34492567-34545860
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1724)
CpG islands
(count:2200)
Chromatin interactive
region (count:155)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1724 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34528420-34528567	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:34528321-34529035	K562	blood:	n/a	n/a
3	ARID3A	chr6:34530717-34531006	K562	blood:	n/a	n/a
4	ARID3A	chr6:34494652-34494762	K562	blood:	n/a	n/a
5	ARID3A	chr6:34495041-34495171	K562	blood:	n/a	n/a
6	ARID3A	chr6:34535143-34535361	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:34537168-34537342	K562	blood:	n/a	n/a
8	ARID3A	chr6:34494959-34495288	HepG2	liver:	n/a	n/a
9	ATF1	chr6:34530640-34531020	K562	blood:	n/a	n/a
10	ATF1	chr6:34528256-34528770	K562	blood:	n/a	n/a
11	ATF1	chr6:34498693-34498808	K562	blood:	n/a	n/a
12	ATF2	chr6:34494984-34495307	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr6:34525098-34525122	K562	blood:	n/a	n/a
14	BACH1	chr6:34494673-34494811	K562	blood:	n/a	n/a
15	BACH1	chr6:34528081-34528565	K562	blood:	n/a	n/a
16	BCL3	chr6:34541372-34541610	GM12878	blood:	n/a	n/a
17	BCL3	chr6:34543140-34543668	K562	blood:	n/a	chr6:34543350-34543359
18	BCL3	chr6:34522693-34523062	GM12878	blood:	n/a	n/a
19	BCL3	chr6:34522720-34523036	GM12878	blood:	n/a	n/a
20	BCLAF1	chr6:34494974-34495328	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:34528358-34529016	HepG2	liver:	n/a	n/a
22	BHLHE40	chr6:34527683-34529135	K562	blood:	n/a	n/a
23	BHLHE40	chr6:34494998-34495331	K562	blood:	n/a	n/a
24	BHLHE40	chr6:34498559-34498914	K562	blood:	n/a	n/a
25	BHLHE40	chr6:34495040-34495240	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:34526077-34526348	K562	blood:	n/a	n/a
27	BHLHE40	chr6:34531305-34531454	K562	blood:	n/a	n/a
28	BHLHE40	chr6:34535821-34536274	HepG2	liver:	n/a	n/a
29	BHLHE40	chr6:34512632-34512964	K562	blood:	n/a	n/a
30	BHLHE40	chr6:34525097-34525230	K562	blood:	n/a	n/a
31	BHLHE40	chr6:34535812-34536294	K562	blood:	n/a	n/a
32	BHLHE40	chr6:34530292-34531071	K562	blood:	n/a	n/a
33	BRCA1	chr6:34528383-34528433	HepG2	liver:	n/a	n/a
34	BRCA1	chr6:34539475-34539630	HepG2	liver:	n/a	n/a
35	BRCA1	chr6:34534813-34534889	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr6:34495142-34495167	HepG2	liver:	n/a	n/a
37	BRCA1	chr6:34495129-34495249	GM12878	blood:	n/a	n/a
38	BRCA1	chr6:34528656-34528787	HepG2	liver:	n/a	n/a
39	CBX3	chr6:34536960-34537774	K562	blood:	n/a	n/a
40	CBX3	chr6:34525771-34526610	K562	blood:	n/a	n/a
41	CBX3	chr6:34504652-34505107	K562	blood:	n/a	n/a
42	CBX3	chr6:34498382-34499182	K562	blood:	n/a	n/a
43	CBX3	chr6:34528147-34529296	K562	blood:	n/a	n/a
44	CBX3	chr6:34504717-34505022	K562	blood:	n/a	n/a
45	CBX3	chr6:34494717-34495375	K562	blood:	n/a	n/a
46	CBX3	chr6:34540358-34540680	K562	blood:	n/a	n/a
47	CBX3	chr6:34525886-34526725	K562	blood:	n/a	n/a
48	CBX3	chr6:34499300-34499739	K562	blood:	n/a	n/a
49	CBX3	chr6:34530537-34531593	K562	blood:	n/a	n/a
50	CBX3	chr6:34528238-34529132	K562	blood:	n/a	n/a

(count:2200 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34528827-34528877	Hela-S3	cervix:	n/a
2	chr6:34543055-34543105	HRPEpiC	eye:	n/a
3	chr6:34524097-34524147	BE2_C	brain:	n/a
4	chr6:34502119-34502169	HRE	kidney:	n/a
5	chr6:34528827-34528877	Hela-S3	cervix:	n/a
6	chr6:34543055-34543105	HRPEpiC	eye:	n/a
7	chr6:34524097-34524147	BE2_C	brain:	n/a
8	chr6:34502119-34502169	HRE	kidney:	n/a
9	chr6:34499488-34499538	AoSMC	blood vessel:	n/a
10	chr6:34513187-34513237	GM12892	blood:	n/a
11	chr6:34524766-34524816	AG04449	skin:	fetal
12	chr6:34494976-34495026	HAEpiC	amniotic membrane:	n/a
13	chr6:34499504-34499554	HCM	heart:	n/a
14	chr6:34501193-34501243	BE2_C	brain:	n/a
15	chr6:34499488-34499538	SAEC	small airway:	n/a
16	chr6:34505610-34505660	Hela-S3	cervix:	n/a
17	chr6:34524290-34524340	SK-N-SH	brain:	n/a
18	chr6:34524290-34524340	GM12878	blood:	n/a
19	chr6:34493129-34493179	A549	lung:	n/a
20	chr6:34535602-34535652	T-47D	breast:	n/a
21	chr6:34513187-34513237	ECC-1	luminal epithelium:	n/a
22	chr6:34524095-34524145	H1-hESC	embryonic stem cell:	embryo
23	chr6:34499314-34499364	GM12878	blood:	n/a
24	chr6:34511514-34511564	LNCaP	prostate:	n/a
25	chr6:34508820-34508870	AG04450	lung:	fetal
26	chr6:34511514-34511564	AG09309	skin:	n/a
27	chr6:34524278-34524328	GM12891	blood:	n/a
28	chr6:34511514-34511564	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:34543055-34543105	HL-60	blood:	n/a
30	chr6:34495393-34495443	K562	blood:	n/a
31	chr6:34495124-34495174	NHDF-neo	bronchial:	n/a
32	chr6:34512083-34512133	GM06990	blood:	n/a
33	chr6:34528827-34528877	MCF-7	breast:	n/a
34	chr6:34524097-34524147	AG09319	gingival:	n/a
35	chr6:34498918-34498968	ProgFib	skin:	n/a
36	chr6:34525026-34525076	HCF	heart:	n/a
37	chr6:34493129-34493179	Hela-S3	cervix:	n/a
38	chr6:34501193-34501243	AG04450	lung:	fetal
39	chr6:34524097-34524147	NH-A	brain:	n/a
40	chr6:34524597-34524647	HEK293	kidney:	embryo
41	chr6:34495292-34495342	SK-N-MC	brain:	n/a
42	chr6:34494976-34495026	A549	lung:	n/a
43	chr6:34504890-34504940	A549	lung:	n/a
44	chr6:34493129-34493179	RPTEC	kidney:	n/a
45	chr6:34495292-34495342	HEK293	kidney:	embryo
46	chr6:34511514-34511564	U87	brain:	n/a
47	chr6:34524097-34524147	SK-N-SH	brain:	n/a
48	chr6:34524097-34524147	SAEC	small airway:	n/a
49	chr6:34513187-34513237	HEEpiC	esophagus:	n/a
50	chr6:34512253-34512303	Jurkat	blood:	n/a

(count:155 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:34535124..34537027-chr6:34540257..34543237,2	K562	blood:
2	chr6:34490944..34493717-chr6:34499736..34502529,2	K562	blood:
3	chr6:33686485..33689308-chr6:34514444..34516167,2	MCF-7	breast:
4	chr6:34529337..34532289-chr6:34533729..34536883,4	K562	blood:
5	chr6:34514887..34517520-chr6:34540730..34542846,2	MCF-7	breast:
6	chr6:34483206..34485571-chr6:34540552..34542756,2	K562	blood:
7	chr6:34535124..34537027-chr6:34540257..34543237,2	K562	blood:
8	chr6:34491359..34493717-chr6:34499044..34502529,3	K562	blood:
9	chr6:34503783..34506203-chr6:34577530..34580135,3	MCF-7	breast:
10	chr6:34506980..34511719-chr6:34518115..34520438,4	K562	blood:
11	chr6:34494680..34495634-chr6:34577124..34578035,2	MCF-7	breast:
12	chr6:34496034..34498791-chr6:34510835..34512433,2	K562	blood:
13	chr6:34502860..34505153-chr6:34574324..34576111,2	MCF-7	breast:
14	chr6:34491195..34497458-chr6:34528901..34533837,5	K562	blood:
15	chr6:34486477..34488245-chr6:34492452..34495163,2	MCF-7	breast:
16	chr6:34509583..34511363-chr6:34518250..34520010,2	K562	blood:
17	chr6:34508361..34510823-chr6:34510978..34513076,2	MCF-7	breast:
18	chr6:34480102..34483166-chr6:34493351..34495807,3	MCF-7	breast:
19	chr6:34524749..34526335-chr6:34530684..34532317,2	K562	blood:
20	chr6:34511760..34514306-chr6:34515453..34517552,2	K562	blood:
21	chr6:34502047..34504010-chr6:34512836..34514494,2	K562	blood:
22	chr6:34494049..34496847-chr6:34497897..34503319,6	K562	blood:
23	chr6:34529351..34531637-chr6:34540105..34542943,4	K562	blood:
24	chr6:34501585..34503222-chr6:34504276..34506644,2	K562	blood:
25	chr6:34502047..34504010-chr6:34512836..34514494,2	K562	blood:
26	chr6:34495305..34497309-chr6:34500179..34501973,2	K562	blood:
27	chr6:34205000..34207351-chr6:34521778..34524214,3	MCF-7	breast:
28	chr6:34382272..34384689-chr6:34494911..34496600,2	K562	blood:
29	chr6:34525385..34526922-chr6:34526989..34528671,2	K562	blood:
30	chr6:34535124..34538612-chr6:34540257..34541806,3	K562	blood:
31	chr6:34528981..34530580-chr6:34530582..34532257,2	MCF-7	breast:
32	chr6:34491359..34493717-chr6:34499044..34502529,3	K562	blood:
33	chr6:34531920..34532420-chr9:133836898..133837416,2	Hela-S3	cervix:
34	chr6:34514736..34516500-chr6:34519380..34521095,2	K562	blood:
35	chr6:34507633..34511172-chr6:34512304..34515175,5	K562	blood:
36	chr6:34490255..34493000-chr6:34512065..34514942,2	K562	blood:
37	chr6:34529351..34531637-chr6:34540105..34542943,4	K562	blood:
38	chr6:34494545..34497462-chr6:34498275..34503019,6	MCF-7	breast:
39	chr6:34514095..34516338-chr6:34543578..34545622,2	MCF-7	breast:
40	chr6:34501160..34503078-chr6:34510332..34511859,2	K562	blood:
41	chr6:34503239..34505474-chr6:34519140..34521426,2	MCF-7	breast:
42	chr6:34527129..34529225-chr6:34531595..34533511,2	K562	blood:
43	chr6:34484087..34487534-chr6:34488647..34495126,10	K562	blood:
44	chr6:34514809..34519137-chr6:34522826..34525341,4	K562	blood:
45	chr6:34496932..34498060-chr6:34528153..34529212,4	MCF-7	breast:
46	chr6:34497242..34499881-chr6:34564591..34566557,2	MCF-7	breast:
47	chr6:34528717..34530463-chr6:34574776..34577421,2	K562	blood:
48	chr6:34521648..34524118-chr6:34538318..34540666,2	MCF-7	breast:
49	chr6:34216948..34217455-chr6:34494244..34495154,2	K562	blood:
50	chr6:34481304..34483971-chr6:34501598..34503855,2	K562	blood:

No data

Variant related genes	Relation type
SPDEF	TF binding region
ENSG00000196114	TF binding region
SPDEF	CpG island
ENSG00000196114	CpG island
ENSG00000186577	chromatin interactions
ENSG00000196114	chromatin interactions
ENSG00000124664	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000223837	chromatin interactions
ENSG00000124614	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000204257	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000124507	chromatin interactions
ENSG00000221635	chromatin interactions

Extended variants
information (count: 2306 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:2306 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186607518	chr6:34492573-34492574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs572698392	chr6:34492587-34492588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536586691	chr6:34492602-34492603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555107437	chr6:34492603-34492604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs74836873	chr6:34492639-34492640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs9380443	chr6:34492642-34492643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543474166	chr6:34492650-34492651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs72898495	chr6:34492668-34492669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556370922	chr6:34492674-34492675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569990440	chr6:34492703-34492704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541004381	chr6:34492726-34492727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs199700121	chr6:34492779-34492780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368095692	chr6:34492780-34492781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556195718	chr6:34492829-34492830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559437936	chr6:34492882-34492883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529992652	chr6:34492956-34492957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191005402	chr6:34492957-34492958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565053129	chr6:34492970-34492971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577571858	chr6:34493010-34493011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs3800466	chr6:34493012-34493013	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs553806130	chr6:34493013-34493014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377003566	chr6:34493030-34493031	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183253485	chr6:34493058-34493059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553849871	chr6:34493129-34493130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571388197	chr6:34493142-34493143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573689459	chr6:34493155-34493156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532518290	chr6:34493185-34493186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547380950	chr6:34493364-34493365	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs116325800	chr6:34493456-34493457	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs141484794	chr6:34493472-34493473	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs112796008	chr6:34493475-34493476	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs146273091	chr6:34493508-34493509	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs374294282	chr6:34493509-34493510	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559221147	chr6:34493515-34493516	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs577009189	chr6:34493543-34493544	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs187643303	chr6:34493557-34493558	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs138115040	chr6:34493644-34493645	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs574371509	chr6:34493651-34493652	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs368241079	chr6:34493675-34493676	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs111501271	chr6:34493708-34493709	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs149534862	chr6:34493748-34493749	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs530864382	chr6:34493904-34493905	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs545592494	chr6:34493906-34493907	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs563982015	chr6:34493964-34493965	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs530982553	chr6:34494025-34494026	Enhancers Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs545786362	chr6:34494033-34494034	Enhancers Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs532431440	chr6:34494051-34494052	Enhancers Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs370901580	chr6:34494054-34494055	Enhancers Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs375420554	chr6:34494057-34494058	Enhancers Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs547491188	chr6:34494062-34494063	Enhancers Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1193 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34441400-34494000	Weak transcription	Right Atrium	heart
2	chr6:34483400-34494200	Weak transcription	Spleen	Spleen
3	chr6:34486400-34493200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:34486600-34493000	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr6:34486800-34494200	Weak transcription	Brain Angular Gyrus	brain
6	chr6:34487800-34494000	Weak transcription	Brain Anterior Caudate	brain
7	chr6:34489000-34495600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr6:34490000-34494000	Weak transcription	Primary B cells from cord blood	blood
9	chr6:34490000-34494000	Weak transcription	Primary B cells from peripheral blood	blood
10	chr6:34490200-34494200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr6:34490200-34494200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:34490400-34494400	Weak transcription	Primary hematopoietic stem cells	blood
13	chr6:34490800-34494200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr6:34491200-34494200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr6:34491600-34495200	Enhancers	Fetal Stomach	stomach
16	chr6:34492000-34493000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr6:34492000-34494200	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr6:34492200-34494200	Enhancers	K562	blood
19	chr6:34492400-34492600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:34492600-34492800	Enhancers	Fetal Kidney	kidney
21	chr6:34492600-34493200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr6:34492600-34494800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr6:34492800-34494600	Weak transcription	Fetal Kidney	kidney
24	chr6:34493000-34493200	Enhancers	Fetal Lung	lung
25	chr6:34493000-34494200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr6:34493000-34494600	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr6:34493200-34493400	Enhancers	H1 Cell Line	embryonic stem cell
28	chr6:34493200-34493800	Weak transcription	Fetal Lung	lung
29	chr6:34493200-34494400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr6:34493200-34494600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr6:34493200-34495200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr6:34493200-34495200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr6:34493400-34493800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr6:34493400-34494200	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr6:34493600-34494400	Enhancers	Brain Cingulate Gyrus	brain
36	chr6:34493600-34495200	Enhancers	Fetal Heart	heart
37	chr6:34493800-34494200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr6:34493800-34494600	Enhancers	Fetal Lung	lung
39	chr6:34494000-34494200	Enhancers	Adipose Nuclei	Adipose
40	chr6:34494000-34494200	Active TSS	Colon Smooth Muscle	Colon
41	chr6:34494000-34494200	Enhancers	Right Atrium	heart
42	chr6:34494000-34494200	Bivalent Enhancer	HepG2	liver
43	chr6:34494000-34494400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr6:34494000-34494400	Enhancers	Brain Anterior Caudate	brain
45	chr6:34494000-34494400	Enhancers	Stomach Smooth Muscle	stomach
46	chr6:34494000-34494800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr6:34494000-34495000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr6:34494000-34495200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr6:34494000-34495200	Enhancers	Colonic Mucosa	Colon
50	chr6:34494000-34495400	Active TSS	Rectal Smooth Muscle	rectum

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