Variant report

Variant	esv16596
Chromosome Location	chr6:119251007-119272087
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:552)
CpG islands
(count:552)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:119255836-119256036	HepG2	liver:	n/a	n/a
2	ATF2	chr6:119255596-119256233	GM12878	blood:	n/a	n/a
3	BCLAF1	chr6:119255934-119256470	GM12878	blood:	n/a	chr6:119256194-119256207
4	BHLHE40	chr6:119255367-119256535	HepG2	liver:	n/a	n/a
5	BHLHE40	chr6:119255476-119256552	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:119255711-119256619	K562	blood:	n/a	n/a
7	BRCA1	chr6:119255930-119256141	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr6:119256054-119256142	GM12878	blood:	n/a	n/a
9	CBX3	chr6:119257336-119257795	K562	blood:	n/a	n/a
10	CBX3	chr6:119266342-119266747	K562	blood:	n/a	n/a
11	CBX3	chr6:119255605-119256632	K562	blood:	n/a	n/a
12	CBX3	chr6:119257135-119257978	K562	blood:	n/a	n/a
13	CCNT2	chr6:119255564-119256544	K562	blood:	n/a	n/a
14	CEBPB	chr6:119254904-119254907	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr6:119255994-119256184	HepG2	liver:	n/a	n/a
16	CEBPB	chr6:119254797-119255085	HepG2	liver:	n/a	chr6:119255048-119255061
17	CEBPB	chr6:119255911-119256551	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:119254836-119255047	A549	lung:	n/a	n/a
19	CEBPB	chr6:119254752-119255061	Hela-S3	cervix:	n/a	chr6:119255048-119255061
20	CEBPD	chr6:119255588-119256470	HepG2	liver:	n/a	n/a
21	CEBPD	chr6:119255608-119256631	K562	blood:	n/a	n/a
22	CHD1	chr6:119255863-119256021	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr6:119255821-119256107	GM12878	blood:	n/a	n/a
24	CHD1	chr6:119256534-119256568	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr6:119255778-119256487	HepG2	liver:	n/a	chr6:119256389-119256399
26	CHD2	chr6:119255503-119256138	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr6:119256364-119256559	H1-hESC	embryonic stem cell:	n/a	chr6:119256389-119256399
28	CHD2	chr6:119255512-119256455	GM12878	blood:	n/a	chr6:119256389-119256399
29	CHD2	chr6:119255757-119256202	K562	blood:	n/a	n/a
30	CHD2	chr6:119255663-119256583	Hela-S3	cervix:	n/a	chr6:119256389-119256399
31	CREB1	chr6:119255995-119256467	A549	lung:	n/a	n/a
32	CREB1	chr6:119255500-119256594	K562	blood:	n/a	n/a
33	CREB1	chr6:119255445-119256645	HepG2	liver:	n/a	n/a
34	CTCF	chr6:119251920-119252070	BJ	skin:	n/a	n/a
35	CTCF	chr6:119251960-119252110	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr6:119251920-119252070	HAc	cerebellar:	n/a	n/a
37	CTCF	chr6:119256060-119256210	GM12874	blood:	n/a	n/a
38	CTCF	chr6:119251940-119252090	HCT-116	colon:	n/a	n/a
39	CTCF	chr6:119251880-119252030	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr6:119252000-119252150	HVMF	connective:	n/a	n/a
41	CTCF	chr6:119251980-119252130	AG09319	gingival:	n/a	n/a
42	CTCF	chr6:119252080-119252230	AG04450	lung:	n/a	n/a
43	CTCF	chr6:119251980-119252130	HPF	lung:	n/a	n/a
44	CTCF	chr6:119251955-119252131	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr6:119256120-119256270	GM12871	blood:	n/a	n/a
46	CTCF	chr6:119251960-119252110	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr6:119252013-119252173	K562	blood:	n/a	n/a
48	CTCF	chr6:119251980-119252130	HMEC	breast:	n/a	n/a
49	CTCF	chr6:119252020-119252170	HepG2	liver:	n/a	n/a
50	CTCF	chr6:119251960-119252110	HBMEC	blood vessel:	n/a	n/a

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:119252835-119252885	H1-hESC	embryonic stem cell:	embryo
2	chr6:119256162-119256212	AG09319	gingival:	n/a
3	chr6:119255874-119255924	T-47D	breast:	n/a
4	chr6:119252835-119252885	H1-hESC	embryonic stem cell:	embryo
5	chr6:119256162-119256212	AG09319	gingival:	n/a
6	chr6:119255874-119255924	T-47D	breast:	n/a
7	chr6:119256162-119256212	NHDF-neo	bronchial:	n/a
8	chr6:119256453-119256503	ECC-1	luminal epithelium:	n/a
9	chr6:119255801-119255851	AoSMC	blood vessel:	n/a
10	chr6:119255801-119255851	CMK	blood:	n/a
11	chr6:119256092-119256142	HIPEpiC	eye:	n/a
12	chr6:119256284-119256334	HL-60	blood:	n/a
13	chr6:119255874-119255924	HNPCEpiC	eye:	n/a
14	chr6:119255801-119255851	ovcar-3	ovarian:	n/a
15	chr6:119256466-119256516	NH-A	brain:	n/a
16	chr6:119255874-119255924	MCF-7	breast:	n/a
17	chr6:119255874-119255924	GM12891	blood:	n/a
18	chr6:119252835-119252885	BJ	skin:	n/a
19	chr6:119256453-119256503	SAEC	small airway:	n/a
20	chr6:119255801-119255851	HPAEpiC	pulmonary alveolar:	n/a
21	chr6:119255812-119255862	AG09319	gingival:	n/a
22	chr6:119256284-119256334	HRPEpiC	eye:	n/a
23	chr6:119256284-119256334	BE2_C	brain:	n/a
24	chr6:119256092-119256142	NT2-D1	testis:	n/a
25	chr6:119255801-119255851	T-47D	breast:	n/a
26	chr6:119256466-119256516	ECC-1	luminal epithelium:	n/a
27	chr6:119255801-119255851	HEK293	kidney:	embryo
28	chr6:119252835-119252885	HMEC	breast:	n/a
29	chr6:119252835-119252885	GM12878	blood:	n/a
30	chr6:119255801-119255851	AG04450	lung:	fetal
31	chr6:119255874-119255924	IMR90	lung:	fetal
32	chr6:119256162-119256212	BE2_C	brain:	n/a
33	chr6:119255874-119255924	SK-N-MC	brain:	n/a
34	chr6:119256466-119256516	Caco-2	colon:	n/a
35	chr6:119256453-119256503	Hepatocyte	liver:	n/a
36	chr6:119256284-119256334	AG09319	gingival:	n/a
37	chr6:119255812-119255862	HAEpiC	amniotic membrane:	n/a
38	chr6:119252835-119252885	A549	lung:	n/a
39	chr6:119255812-119255862	HL-60	blood:	n/a
40	chr6:119255812-119255862	CMK	blood:	n/a
41	chr6:119255812-119255862	H1-hESC	embryonic stem cell:	embryo
42	chr6:119256162-119256212	PFSK-1	brain:	n/a
43	chr6:119256453-119256503	HL-60	blood:	n/a
44	chr6:119256162-119256212	NB4	blood:	n/a
45	chr6:119255812-119255862	PrEC	prostate:	n/a
46	chr6:119256162-119256212	NT2-D1	testis:	n/a
47	chr6:119256453-119256503	HRCEpiC	kidney:	n/a
48	chr6:119256162-119256212	SAEC	small airway:	n/a
49	chr6:119256162-119256212	CMK	blood:	n/a
50	chr6:119256092-119256142	NHDF-neo	bronchial:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:119220702..119224795-chr6:119249246..119252141,5	K562	blood:
2	chr6:119235128..119240237-chr6:119246100..119252076,6	K562	blood:
3	chr6:119264941..119267288-chr6:119996972..119999552,2	K562	blood:
4	chr6:119225449..119227305-chr6:119252060..119254076,2	K562	blood:
5	chr6:119213694..119219544-chr6:119251621..119258172,21	K562	blood:
6	chr6:119230305..119231903-chr6:119251881..119253560,2	K562	blood:
7	chr6:119255727..119258203-chr6:119400226..119402388,2	K562	blood:
8	chr6:119257082..119259694-chr6:119259960..119261722,2	K562	blood:
9	chr6:119256106..119257947-chr6:119468580..119471034,2	K562	blood:
10	chr4:79472622..79473237-chr6:119256049..119256758,2	HCT-116	colon:
11	chr6:119256349..119258481-chr6:119264695..119266812,2	K562	blood:
12	chr15:90708735..90709594-chr6:119255785..119256642,2	HCT-116	colon:
13	chr6:119246982..119248806-chr6:119249429..119252283,2	K562	blood:
14	chr6:119214552..119219906-chr6:119253918..119257622,8	MCF-7	breast:
15	chr6:119255269..119257410-chr6:119258085..119262508,5	MCF-7	breast:
16	chr6:119256349..119258481-chr6:119264695..119266812,2	K562	blood:
17	chr6:119213036..119217484-chr6:119254311..119257675,9	MCF-7	breast:
18	chr3:155571664..155572210-chr6:119255210..119256056,2	Hela-S3	cervix:
19	chr6:119216722..119218492-chr6:119251658..119253168,2	K562	blood:
20	chr6:119253238..119258280-chr6:119398045..119402661,8	K562	blood:
21	chr6:119242613..119249110-chr6:119251513..119257145,6	MCF-7	breast:
22	chr10:74927354..74928318-chr6:119255751..119256642,2	NB4	blood:
23	chr6:119256205..119257932-chr6:119293855..119296677,2	K562	blood:
24	chr6:119235730..119238725-chr6:119250576..119253329,2	K562	blood:
25	chr6:119213105..119220728-chr6:119253299..119257962,22	K562	blood:
26	chr5:56205869..56206380-chr6:119255621..119256581,2	Hela-S3	cervix:
27	chr1:149223435..149224292-chr6:119255876..119256729,2	HCT-116	colon:
28	chr6:119255888..119257460-chr6:119263231..119265937,2	MCF-7	breast:
29	chr6:119250858..119252631-chr6:119254027..119256960,4	MCF-7	breast:
30	chr6:119256460..119259122-chr6:119259921..119263121,4	K562	blood:
31	chr6:119257082..119259694-chr6:119259960..119261722,2	K562	blood:
32	chr6:119252974..119255408-chr6:119376994..119379902,2	K562	blood:
33	chr6:119256460..119259122-chr6:119259921..119263121,4	K562	blood:
34	chr6:119251278..119254603-chr6:119254723..119256647,5	MCF-7	breast:
35	chr6:119253156..119256806-chr6:119394976..119399977,7	K562	blood:
36	chr6:119230403..119232175-chr6:119251881..119254660,2	K562	blood:
37	chr1:28907889..28908475-chr6:119255713..119256233,2	Hela-S3	cervix:
38	chr6:119148024..119150788-chr6:119254470..119256543,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000253194	TF binding region
MCM9	TF binding region
ENSG00000253194	CpG island
MCM9	CpG island
ENSG00000206737	chromatin interactions
ENSG00000111877	chromatin interactions
ENSG00000222649	chromatin interactions
ENSG00000122882	chromatin interactions
ENSG00000111875	chromatin interactions
ENSG00000253194	chromatin interactions
ENSG00000240470	chromatin interactions
ENSG00000155542	chromatin interactions
ENSG00000197989	chromatin interactions
ENSG00000169359	chromatin interactions
ENSG00000138286	chromatin interactions
ENSG00000138772	chromatin interactions
ENSG00000111879	chromatin interactions

Extended variants
information (count: 750 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:750 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190950428	chr6:119251008-119251009	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs75379834	chr6:119251029-119251030	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs183135351	chr6:119251042-119251043	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs532592133	chr6:119251078-119251079	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs531030138	chr6:119251199-119251200	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs186659404	chr6:119251213-119251214	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs554931394	chr6:119251251-119251252	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs141869584	chr6:119251267-119251268	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs149465777	chr6:119251268-119251269	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs35247641	chr6:119251269-119251270	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs4027511	chr6:119251271-119251272	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs560338536	chr6:119251299-119251300	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs527468958	chr6:119251301-119251302	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs547195703	chr6:119251306-119251307	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs62422262	chr6:119251307-119251308	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs191111326	chr6:119251314-119251315	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs554318368	chr6:119251327-119251328	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs567531214	chr6:119251332-119251333	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs11153781	chr6:119251338-119251339	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs542131134	chr6:119251339-119251340	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs141311693	chr6:119251345-119251346	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs562216255	chr6:119251368-119251369	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs527712534	chr6:119251377-119251378	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs576506212	chr6:119251417-119251418	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs188172677	chr6:119251420-119251421	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs112036562	chr6:119251421-119251422	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs185313551	chr6:119251425-119251426	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs62422263	chr6:119251431-119251432	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs62422264	chr6:119251432-119251433	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs539799635	chr6:119251442-119251443	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs561948539	chr6:119251464-119251465	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs553570010	chr6:119251467-119251468	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs190115065	chr6:119251479-119251480	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs572627168	chr6:119251488-119251489	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs12234152	chr6:119251502-119251503	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs12234153	chr6:119251512-119251513	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs9489547	chr6:119251523-119251524	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs533452134	chr6:119251525-119251526	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs192589921	chr6:119251528-119251529	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs12234134	chr6:119251529-119251530	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs567054124	chr6:119251557-119251558	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs200813303	chr6:119251559-119251560	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs148309190	chr6:119251567-119251568	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs549615846	chr6:119251573-119251574	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs567737438	chr6:119251604-119251605	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs550555079	chr6:119251699-119251700	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs1022709	chr6:119251706-119251707	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs570253217	chr6:119251806-119251807	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs539144075	chr6:119251842-119251843	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs184738373	chr6:119251880-119251881	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	18698023	CNVD
Mental retardation	18854857	CNVD
Leukemia	18688285	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Liver carcinoma	19366792	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:706 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119219200-119254000	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr6:119219200-119254400	Strong transcription	Placenta	Placenta
3	chr6:119219600-119253000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr6:119219600-119253800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr6:119221200-119255800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:119222000-119254000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:119222000-119254400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:119222000-119255200	Weak transcription	Fetal Heart	heart
9	chr6:119222200-119253400	Strong transcription	Fetal Intestine Large	intestine
10	chr6:119222600-119251400	Strong transcription	Dnd41	blood
11	chr6:119222600-119253800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr6:119222600-119253800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr6:119224000-119254000	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr6:119224200-119252800	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr6:119224600-119254000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr6:119224800-119254800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr6:119226000-119255200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr6:119227000-119254800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr6:119227400-119252000	Weak transcription	Small Intestine	intestine
20	chr6:119227400-119253800	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr6:119227800-119254800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr6:119228000-119253000	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr6:119228200-119253400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr6:119235600-119255200	Weak transcription	Fetal Brain Male	brain
25	chr6:119235600-119255400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr6:119236000-119253400	Strong transcription	Liver	Liver
27	chr6:119236600-119254000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:119236600-119255200	Weak transcription	Right Ventricle	heart
29	chr6:119237000-119255200	Weak transcription	Brain Germinal Matrix	brain
30	chr6:119237000-119255200	Weak transcription	Gastric	stomach
31	chr6:119237200-119255200	Weak transcription	Brain Angular Gyrus	brain
32	chr6:119239600-119253800	Strong transcription	Primary B cells from cord blood	blood
33	chr6:119239800-119255200	Weak transcription	NHLF	lung
34	chr6:119240000-119255200	Weak transcription	Fetal Brain Female	brain
35	chr6:119240400-119252800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr6:119241000-119254800	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr6:119242600-119255200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr6:119242600-119255200	Weak transcription	Colonic Mucosa	Colon
39	chr6:119242800-119252600	Weak transcription	NHDF-Ad	bronchial
40	chr6:119242800-119255800	Weak transcription	Spleen	Spleen
41	chr6:119243000-119251800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr6:119243000-119255200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr6:119243400-119253600	Weak transcription	Stomach Mucosa	stomach
44	chr6:119243400-119255200	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr6:119243600-119254000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr6:119243800-119254800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr6:119243800-119254800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr6:119244000-119252000	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr6:119244000-119255200	Weak transcription	Brain Cingulate Gyrus	brain
50	chr6:119244000-119255400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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