Variant report

Variant	esv990390
Chromosome Location	chr15:75179300-75187945
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:624)
CpG islands
(count:734)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:624 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:75182204-75182592	K562	blood:	n/a	n/a
2	ARID3A	chr15:75182199-75182490	HepG2	liver:	n/a	n/a
3	ATF1	chr15:75182194-75182566	K562	blood:	n/a	n/a
4	ATF2	chr15:75181955-75182592	GM12878	blood:	n/a	n/a
5	BACH1	chr15:75183272-75183467	K562	blood:	n/a	n/a
6	BACH1	chr15:75182333-75182672	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr15:75181191-75181196	K562	blood:	n/a	n/a
8	BCL3	chr15:75181547-75181895	GM12878	blood:	n/a	n/a
9	BCL3	chr15:75182041-75182916	A549	lung:	n/a	chr15:75182358-75182371
10	BCL3	chr15:75181839-75182906	A549	lung:	n/a	chr15:75182358-75182371
11	BCLAF1	chr15:75181951-75182652	GM12878	blood:	n/a	chr15:75182358-75182371
12	BHLHE40	chr15:75181882-75182634	K562	blood:	n/a	chr15:75182358-75182374
13	BHLHE40	chr15:75181960-75182564	HepG2	liver:	n/a	chr15:75182358-75182374
14	BHLHE40	chr15:75182070-75182511	GM12878	blood:	n/a	chr15:75182358-75182374
15	BRCA1	chr15:75182513-75182537	HepG2	liver:	n/a	n/a
16	BRCA1	chr15:75182216-75182492	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr15:75183155-75183248	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr15:75181646-75182637	K562	blood:	n/a	n/a
19	CCNT2	chr15:75182222-75182602	K562	blood:	n/a	chr15:75182592-75182601
20	CEBPB	chr15:75182142-75182450	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr15:75184731-75185011	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr15:75181928-75182068	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr15:75183066-75183255	K562	blood:	n/a	n/a
24	CEBPB	chr15:75184596-75185017	MCF-7	breast:	n/a	n/a
25	CEBPD	chr15:75182249-75182572	HepG2	liver:	n/a	n/a
26	CHD1	chr15:75182179-75182585	GM12878	blood:	n/a	n/a
27	CHD2	chr15:75182297-75182562	HepG2	liver:	n/a	n/a
28	CHD2	chr15:75182043-75182493	K562	blood:	n/a	n/a
29	CHD2	chr15:75182175-75182599	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr15:75182181-75182570	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr15:75184898-75184932	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr15:75182184-75182583	GM12878	blood:	n/a	n/a
33	CREB1	chr15:75181650-75182900	HepG2	liver:	n/a	n/a
34	CREB1	chr15:75182161-75182681	A549	lung:	n/a	n/a
35	CREB1	chr15:75182011-75182758	HepG2	liver:	n/a	n/a
36	CREB1	chr15:75182067-75182930	GM12878	blood:	n/a	n/a
37	CREB1	chr15:75182104-75183027	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr15:75182153-75182517	A549	lung:	n/a	n/a
39	CREB1	chr15:75182106-75182881	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr15:75182409-75182441	GM12891	blood:	n/a	n/a
41	CTCF	chr15:75184900-75185050	HMEC	breast:	n/a	n/a
42	CTCF	chr15:75182300-75182450	AG04449	skin:	n/a	n/a
43	CTCF	chr15:75184940-75185090	NHEK	skin:	n/a	n/a
44	CTCF	chr15:75182180-75182330	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr15:75182320-75182470	HMEC	breast:	n/a	n/a
46	CTCF	chr15:75182260-75182410	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr15:75184831-75185026	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:75182340-75182490	GM12865	blood:	n/a	n/a
49	CTCF	chr15:75184847-75185015	MCF-7	breast:	n/a	n/a
50	CTCF	chr15:75182600-75182750	HAc	cerebellar:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75182130-75182180	AG09309	skin:	n/a
2	chr15:75182886-75182936	U87	brain:	n/a
3	chr15:75182130-75182180	AG09309	skin:	n/a
4	chr15:75182886-75182936	U87	brain:	n/a
5	chr15:75182455-75182505	LNCaP	prostate:	n/a
6	chr15:75181202-75181252	SK-N-SH	brain:	n/a
7	chr15:75182351-75182401	HMEC	breast:	n/a
8	chr15:75182516-75182566	LNCaP	prostate:	n/a
9	chr15:75182231-75182281	BE2_C	brain:	n/a
10	chr15:75182590-75182640	LNCaP	prostate:	n/a
11	chr15:75182455-75182505	BE2_C	brain:	n/a
12	chr15:75182231-75182281	T-47D	breast:	n/a
13	chr15:75182516-75182566	MCF10A-Er-Src	breast:	n/a
14	chr15:75182590-75182640	NHBE	bronchial:	n/a
15	chr15:75182292-75182342	NHBE	bronchial:	n/a
16	chr15:75181202-75181252	HIPEpiC	eye:	n/a
17	chr15:75182410-75182460	SAEC	small airway:	n/a
18	chr15:75182292-75182342	AG04449	skin:	fetal
19	chr15:75182373-75182423	MCF-7	breast:	n/a
20	chr15:75182886-75182936	AG09319	gingival:	n/a
21	chr15:75182886-75182936	AG10803	skin:	n/a
22	chr15:75181202-75181252	LNCaP	prostate:	n/a
23	chr15:75181202-75181252	Caco-2	colon:	n/a
24	chr15:75181202-75181252	GM12892	blood:	n/a
25	chr15:75182455-75182505	HepG2	liver:	n/a
26	chr15:75181202-75181252	SK-N-MC	brain:	n/a
27	chr15:75182373-75182423	SK-N-SH	brain:	n/a
28	chr15:75182351-75182401	NB4	blood:	n/a
29	chr15:75182455-75182505	H1-hESC	embryonic stem cell:	embryo
30	chr15:75182590-75182640	HepG2	liver:	n/a
31	chr15:75182516-75182566	SKMC	muscle:	n/a
32	chr15:75182351-75182401	SK-N-SH	brain:	n/a
33	chr15:75182455-75182505	ProgFib	skin:	n/a
34	chr15:75182231-75182281	RPTEC	kidney:	n/a
35	chr15:75182292-75182342	HepG2	liver:	n/a
36	chr15:75182231-75182281	HL-60	blood:	n/a
37	chr15:75182231-75182281	GM12891	blood:	n/a
38	chr15:75182410-75182460	PrEC	prostate:	n/a
39	chr15:75182516-75182566	SK-N-MC	brain:	n/a
40	chr15:75182455-75182505	HRE	kidney:	n/a
41	chr15:75182351-75182401	BE2_C	brain:	n/a
42	chr15:75182886-75182936	HMEC	breast:	n/a
43	chr15:75185989-75186039	AG04450	lung:	fetal
44	chr15:75182516-75182566	AG04449	skin:	fetal
45	chr15:75182516-75182566	T-47D	breast:	n/a
46	chr15:75182410-75182460	Caco-2	colon:	n/a
47	chr15:75182351-75182401	IMR90	lung:	fetal
48	chr15:75182292-75182342	AG10803	skin:	n/a
49	chr15:75185989-75186039	HEEpiC	esophagus:	n/a
50	chr15:75182292-75182342	HMEC	breast:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:75072788..75075776-chr15:75181274..75184204,3	K562	blood:
2	chr15:75116359..75118172-chr15:75182130..75184765,2	MCF-7	breast:
3	chr15:75166310..75168984-chr15:75177329..75180043,2	MCF-7	breast:
4	chr15:75109719..75111456-chr15:75185022..75186522,2	MCF-7	breast:
5	chr15:75127539..75130871-chr15:75182053..75185205,4	MCF-7	breast:
6	chr15:74911034..74913432-chr15:75186630..75189281,2	MCF-7	breast:
7	chr15:75142292..75144361-chr15:75184873..75186770,2	K562	blood:
8	chr15:75131329..75142649-chr15:75180088..75200119,60	MCF-7	breast:
9	chr14:20811377..20812189-chr15:75182113..75182904,2	NB4	blood:
10	chr15:75181382..75185367-chr15:75245501..75252189,8	K562	blood:
11	chr15:75178767..75180347-chr15:75180887..75182737,2	MCF-7	breast:
12	chr15:75181982..75182553-chr16:2731901..2732822,2	Hela-S3	cervix:
13	chr15:75181707..75184142-chr2:24161514..24164019,2	MCF-7	breast:
14	chr15:75156545..75159476-chr15:75183223..75185437,3	MCF-7	breast:
15	chr15:75080217..75082228-chr15:75182575..75184955,2	MCF-7	breast:
16	chr15:75182375..75183231-chr16:31191121..31191881,2	Hela-S3	cervix:
17	chr15:75081397..75085815-chr15:75182279..75185381,4	MCF-7	breast:
18	chr15:75185806..75187453-chr15:75190823..75193900,3	MCF-7	breast:
19	chr15:75133950..75137156-chr15:75180779..75184661,9	MCF-7	breast:
20	chr15:75144564..75147431-chr15:75184643..75187545,2	MCF-7	breast:
21	chr15:75180371..75182934-chr15:75228872..75231935,3	MCF-7	breast:
22	chr15:75162469..75167536-chr15:75180880..75184902,6	K562	blood:
23	chr15:75186057..75188212-chr15:75229416..75232067,2	MCF-7	breast:
24	chr15:75167898..75170533-chr15:75183102..75184983,2	K562	blood:
25	chr15:75184447..75185329-chr15:75193714..75194464,2	MCF-7	breast:
26	chr15:75163342..75166719-chr15:75180364..75184673,7	MCF-7	breast:
27	chr15:75072788..75075776-chr15:75181274..75184204,2	K562	blood:
28	chr15:75072512..75079183-chr15:75180576..75186728,11	MCF-7	breast:
29	chr15:75130141..75132356-chr15:75184160..75186177,2	K562	blood:
30	chr15:75184487..75185396-chr15:75193713..75194528,2	MCF-7	breast:
31	chr15:75105024..75106901-chr15:75183732..75185502,2	MCF-7	breast:
32	chr15:75133989..75136127-chr15:75187296..75189781,2	K562	blood:
33	chr12:132413527..132414298-chr15:75182220..75183083,2	Hela-S3	cervix:
34	chr15:75182085..75184679-chr15:75247604..75250598,2	MCF-7	breast:
35	chr15:75133683..75136875-chr15:75181140..75184004,7	K562	blood:
36	chr15:75182007..75182934-chr17:8076332..8076994,2	Hela-S3	cervix:
37	chr15:75180021..75183481-chr15:75226759..75230284,3	K562	blood:
38	chr15:75180806..75183670-chr15:75227670..75231591,7	K562	blood:
39	chr15:75163351..75167012-chr15:75180238..75185061,13	MCF-7	breast:
40	chr15:75184495..75186934-chr15:75223439..75225977,2	K562	blood:
41	chr15:75163901..75170368-chr15:75180139..75184021,10	K562	blood:
42	chr15:75181107..75185393-chr15:75190667..75200295,16	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000260824	TF binding region
MPI	TF binding region
ENSG00000260824	CpG island
MPI	CpG island
ENSG00000260824	chromatin interactions
ENSG00000198794	chromatin interactions
ENSG00000178741	chromatin interactions
ENSG00000255992	chromatin interactions
ENSG00000177192	chromatin interactions
ENSG00000178802	chromatin interactions
ENSG00000129484	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000259001	chromatin interactions
ENSG00000178761	chromatin interactions
ENSG00000264386	chromatin interactions
ENSG00000140474	chromatin interactions
ENSG00000179335	chromatin interactions
ENSG00000200463	chromatin interactions
ENSG00000140497	chromatin interactions
ENSG00000178718	chromatin interactions
ENSG00000173960	chromatin interactions
ENSG00000167977	chromatin interactions
ENSG00000140506	chromatin interactions
ENSG00000103653	chromatin interactions

Extended variants
information (count: 377 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:377 , 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	rs12914755	chr15:75179303-75179304	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs12914770	chr15:75179334-75179335	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs113688239	chr15:75179348-75179349	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531623026	chr15:75179353-75179354	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs12914793	chr15:75179366-75179367	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs12914794	chr15:75179369-75179370	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs12915620	chr15:75179376-75179377	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs12914803	chr15:75179378-75179379	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs542874490	chr15:75179393-75179394	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs77413145	chr15:75179394-75179395	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs571584684	chr15:75179435-75179436	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs576203693	chr15:75179458-75179459	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs543627647	chr15:75179521-75179522	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs7182183	chr15:75179556-75179557	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs547422998	chr15:75179574-75179575	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs184351869	chr15:75179575-75179576	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs532524643	chr15:75179606-75179607	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs541410940	chr15:75179624-75179625	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs567240027	chr15:75179640-75179641	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs370928697	chr15:75179654-75179655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs201174775	chr15:75179657-75179658	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs367694970	chr15:75179674-75179675	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs559525782	chr15:75179777-75179778	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs188387461	chr15:75179878-75179879	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs549252638	chr15:75179904-75179905	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs528713235	chr15:75179918-75179919	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs201074136	chr15:75179954-75179955	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs71434243	chr15:75179956-75179957	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs201681687	chr15:75179988-75179989	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs200384860	chr15:75179995-75179996	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs201163230	chr15:75179996-75179997	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs569467680	chr15:75180024-75180025	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs149891592	chr15:75180042-75180043	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs574088062	chr15:75180056-75180057	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs369106419	chr15:75180067-75180068	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs73436511	chr15:75180101-75180102	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs181166639	chr15:75180116-75180117	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs183120480	chr15:75180127-75180128	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs79774492	chr15:75180130-75180131	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs75156305	chr15:75180131-75180132	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs557984745	chr15:75180139-75180140	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs398099902	chr15:75180142-75180143	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs565491071	chr15:75180146-75180147	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs535865550	chr15:75180186-75180187	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs554805518	chr15:75180193-75180194	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs576359976	chr15:75180200-75180201	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs183551550	chr15:75180218-75180219	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs543591459	chr15:75180233-75180234	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs558934348	chr15:75180234-75180235	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs577260896	chr15:75180239-75180240	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	18438408	CNVD

Chromatin state (count:954 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75166200-75181000	Weak transcription	Fetal Heart	heart
2	chr15:75175200-75181000	Weak transcription	Spleen	Spleen
3	chr15:75175400-75181200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr15:75176800-75181200	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr15:75176800-75181400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr15:75176800-75181800	Weak transcription	A549	lung
7	chr15:75177000-75181200	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr15:75177000-75181800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr15:75177200-75181000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr15:75177200-75181400	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr15:75177200-75181600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr15:75177200-75181800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr15:75177400-75179600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr15:75177400-75181000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr15:75177400-75181200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr15:75177400-75181200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr15:75177400-75181200	Weak transcription	NH-A	brain
18	chr15:75177400-75181400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr15:75177400-75181400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr15:75177400-75181600	Weak transcription	Primary B cells from peripheral blood	blood
21	chr15:75177600-75181000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr15:75177600-75181000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr15:75177600-75181000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr15:75177600-75181000	Weak transcription	HepG2	liver
25	chr15:75177600-75181200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr15:75177600-75181200	Weak transcription	GM12878-XiMat	blood
27	chr15:75177600-75181400	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr15:75177600-75181400	Weak transcription	HSMMtube	muscle
29	chr15:75177600-75181400	Weak transcription	NHLF	lung
30	chr15:75177600-75181400	Weak transcription	Osteobl	bone
31	chr15:75177800-75181000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr15:75177800-75181000	Weak transcription	Placenta	Placenta
33	chr15:75177800-75181400	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr15:75177800-75181400	Weak transcription	Hela-S3	cervix
35	chr15:75177800-75181600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr15:75178000-75181000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr15:75178000-75181000	Weak transcription	Adipose Nuclei	Adipose
38	chr15:75178000-75181200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr15:75178000-75181200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr15:75178000-75181200	Weak transcription	NHEK	skin
41	chr15:75178000-75181400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr15:75178000-75181400	Weak transcription	HMEC	breast
43	chr15:75178000-75181400	Weak transcription	HSMM	muscle
44	chr15:75178200-75181200	Weak transcription	NHDF-Ad	bronchial
45	chr15:75178400-75180000	Enhancers	K562	blood
46	chr15:75178600-75181000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr15:75178800-75179400	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr15:75178800-75181200	Weak transcription	Fetal Intestine Small	intestine
49	chr15:75179000-75181000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr15:75179000-75181400	Weak transcription	Fetal Intestine Large	intestine

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