Variant report

Variant	nsv1026597
Chromosome Location	chr6:13634669-13689882
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:730)
CpG islands
(count:61)
Chromatin interactive
region (count:121)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:730 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:13674342-13675923	K562	blood:	n/a	n/a
2	ARID3A	chr6:13664966-13665341	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:13688902-13689192	K562	blood:	n/a	n/a
4	ARID3A	chr6:13663839-13664278	K562	blood:	n/a	n/a
5	ARID3A	chr6:13678126-13678467	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:13665044-13665259	K562	blood:	n/a	n/a
7	ARID3A	chr6:13676179-13676334	K562	blood:	n/a	n/a
8	ARID3A	chr6:13678173-13679433	K562	blood:	n/a	n/a
9	ARID3A	chr6:13664506-13664781	K562	blood:	n/a	n/a
10	ARID3A	chr6:13665662-13667524	K562	blood:	n/a	n/a
11	ARID3A	chr6:13668367-13669587	K562	blood:	n/a	n/a
12	ARID3A	chr6:13676883-13677295	K562	blood:	n/a	n/a
13	ARID3A	chr6:13661929-13662252	K562	blood:	n/a	n/a
14	ATF1	chr6:13688925-13689257	K562	blood:	n/a	n/a
15	ATF1	chr6:13666244-13666462	K562	blood:	n/a	n/a
16	ATF1	chr6:13668855-13669090	K562	blood:	n/a	n/a
17	ATF1	chr6:13678107-13679032	K562	blood:	n/a	n/a
18	ATF1	chr6:13674729-13675459	K562	blood:	n/a	n/a
19	ATF2	chr6:13681682-13682169	GM12878	blood:	n/a	n/a
20	ATF3	chr6:13678506-13679232	K562	blood:	n/a	n/a
21	ATF3	chr6:13688859-13689310	K562	blood:	n/a	n/a
22	BACH1	chr6:13668769-13669114	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr6:13679300-13679387	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr6:13668757-13669164	K562	blood:	n/a	n/a
25	BACH1	chr6:13664104-13664201	K562	blood:	n/a	n/a
26	BACH1	chr6:13675327-13675447	K562	blood:	n/a	n/a
27	BCLAF1	chr6:13674974-13675606	K562	blood:	n/a	n/a
28	BCLAF1	chr6:13678453-13679431	K562	blood:	n/a	n/a
29	BHLHE40	chr6:13682121-13682130	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:13689061-13689157	K562	blood:	n/a	n/a
31	BHLHE40	chr6:13675323-13675393	K562	blood:	n/a	n/a
32	BHLHE40	chr6:13678580-13679057	K562	blood:	n/a	n/a
33	BHLHE40	chr6:13674936-13674960	K562	blood:	n/a	n/a
34	BRCA1	chr6:13665116-13665306	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr6:13664730-13664871	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr6:13661827-13662388	K562	blood:	n/a	n/a
37	CBX3	chr6:13688782-13689512	K562	blood:	n/a	n/a
38	CBX3	chr6:13668804-13669236	K562	blood:	n/a	n/a
39	CBX3	chr6:13674973-13675420	K562	blood:	n/a	n/a
40	CBX3	chr6:13688898-13689385	K562	blood:	n/a	n/a
41	CBX3	chr6:13676635-13677433	K562	blood:	n/a	n/a
42	CBX3	chr6:13668798-13669255	K562	blood:	n/a	n/a
43	CBX3	chr6:13677905-13679030	K562	blood:	n/a	n/a
44	CBX3	chr6:13676535-13677572	K562	blood:	n/a	n/a
45	CBX3	chr6:13670195-13670853	K562	blood:	n/a	n/a
46	CBX3	chr6:13674593-13675502	K562	blood:	n/a	n/a
47	CBX3	chr6:13677910-13679125	K562	blood:	n/a	n/a
48	CCNT2	chr6:13651152-13651187	K562	blood:	n/a	n/a
49	CCNT2	chr6:13678504-13679032	K562	blood:	n/a	n/a
50	CCNT2	chr6:13665186-13665276	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:13639938-13639988	NHDF-neo	bronchial:	n/a
2	chr6:13639938-13639988	HCT-116	colon:	n/a
3	chr6:13639938-13639988	T-47D	breast:	n/a
4	chr6:13639938-13639988	AG10803	skin:	n/a
5	chr6:13639938-13639988	GM12878	blood:	n/a
6	chr6:13639938-13639988	MCF10A-Er-Src	breast:	n/a
7	chr6:13639938-13639988	HAEpiC	amniotic membrane:	n/a
8	chr6:13639938-13639988	HRE	kidney:	n/a
9	chr6:13639938-13639988	IMR90	lung:	fetal
10	chr6:13639938-13639988	HIPEpiC	eye:	n/a
11	chr6:13639938-13639988	GM12892	blood:	n/a
12	chr6:13639938-13639988	AG09309	skin:	n/a
13	chr6:13639938-13639988	AG04449	skin:	fetal
14	chr6:13639938-13639988	SK-N-SH_RA	brain:	n/a
15	chr6:13639938-13639988	PrEC	prostate:	n/a
16	chr6:13639938-13639988	HUVEC	blood vessel:	n/a
17	chr6:13639938-13639988	HRCEpiC	kidney:	n/a
18	chr6:13639938-13639988	BE2_C	brain:	n/a
19	chr6:13639938-13639988	HL-60	blood:	n/a
20	chr6:13639938-13639988	GM12891	blood:	n/a
21	chr6:13639938-13639988	LNCaP	prostate:	n/a
22	chr6:13639938-13639988	H1-hESC	embryonic stem cell:	embryo
23	chr6:13639938-13639988	PFSK-1	brain:	n/a
24	chr6:13639938-13639988	SK-N-MC	brain:	n/a
25	chr6:13639938-13639988	K562	blood:	n/a
26	chr6:13639938-13639988	HNPCEpiC	eye:	n/a
27	chr6:13639938-13639988	SKMC	muscle:	n/a
28	chr6:13639938-13639988	GM06990	blood:	n/a
29	chr6:13639938-13639988	ProgFib	skin:	n/a
30	chr6:13639938-13639988	GM19239	blood:	n/a
31	chr6:13639938-13639988	BJ	skin:	n/a
32	chr6:13639938-13639988	HEK293	kidney:	embryo
33	chr6:13639938-13639988	NHBE	bronchial:	n/a
34	chr6:13639938-13639988	HCF	heart:	n/a
35	chr6:13639938-13639988	AG04450	lung:	fetal
36	chr6:13639938-13639988	AoSMC	blood vessel:	n/a
37	chr6:13639938-13639988	A549	lung:	n/a
38	chr6:13639938-13639988	Caco-2	colon:	n/a
39	chr6:13639938-13639988	SAEC	small airway:	n/a
40	chr6:13639938-13639988	NT2-D1	testis:	n/a
41	chr6:13639938-13639988	HPAEpiC	pulmonary alveolar:	n/a
42	chr6:13639938-13639988	HepG2	liver:	n/a
43	chr6:13639938-13639988	Jurkat	blood:	n/a
44	chr6:13639938-13639988	U87	brain:	n/a
45	chr6:13639938-13639988	HCM	heart:	n/a
46	chr6:13639938-13639988	HRPEpiC	eye:	n/a
47	chr6:13639938-13639988	AG09319	gingival:	n/a
48	chr6:13639938-13639988	HCPEpiC	choroid plexus:	n/a
49	chr6:13639938-13639988	MCF-7	breast:	n/a
50	chr6:13639938-13639988	Hela-S3	cervix:	n/a

(count:121 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:13614016..13617291-chr6:13638337..13642167,4	K562	blood:
2	chr6:13649255..13650817-chr6:13651728..13653387,2	K562	blood:
3	chr6:13656757..13659128-chr6:13659241..13662282,5	K562	blood:
4	chr6:13688697..13690982-chr6:13709876..13712249,2	MCF-7	breast:
5	chr6:13630729..13632300-chr6:13635743..13637906,2	K562	blood:
6	chr6:13683067..13686006-chr6:13687283..13690092,3	MCF-7	breast:
7	chr6:13573533..13576105-chr6:13657516..13659803,2	K562	blood:
8	chr6:13644070..13647377-chr6:13677584..13680822,4	K562	blood:
9	chr6:13641812..13646740-chr6:13710495..13713683,5	K562	blood:
10	chr6:13656757..13659128-chr6:13659241..13662282,5	K562	blood:
11	chr6:13644681..13646353-chr6:13651574..13653545,2	K562	blood:
12	chr6:13664693..13668460-chr6:13708038..13711894,3	K562	blood:
13	chr6:13633189..13636123-chr6:13700882..13703156,2	K562	blood:
14	chr6:13647295..13649197-chr6:13661190..13662891,2	K562	blood:
15	chr6:13658437..13687167-chr6:13707669..13717356,51	K562	blood:
16	chr6:13651237..13655729-chr6:13659115..13661394,7	K562	blood:
17	chr6:13662280..13665137-chr6:13691435..13693761,2	K562	blood:
18	chr6:13644488..13646083-chr6:13662452..13664721,2	K562	blood:
19	chr6:13649508..13651998-chr6:13682343..13685063,2	K562	blood:
20	chr6:13636958..13639286-chr6:13678817..13681067,2	K562	blood:
21	chr6:13682245..13684972-chr6:13710656..13712601,2	MCF-7	breast:
22	chr6:13667308..13669773-chr6:13712805..13714594,2	K562	blood:
23	chr6:13678917..13680916-chr6:13684089..13685719,2	MCF-7	breast:
24	chr6:13614062..13615646-chr6:13642570..13644514,2	K562	blood:
25	chr6:13613711..13616246-chr6:13670617..13673188,4	K562	blood:
26	chr6:13614409..13618371-chr6:13665029..13668940,4	K562	blood:
27	chr6:13688579..13690387-chr6:13690933..13692807,2	MCF-7	breast:
28	chr6:13622245..13624613-chr6:13641011..13644598,3	K562	blood:
29	chr6:13644488..13646083-chr6:13662452..13664721,2	K562	blood:
30	chr6:13572493..13576795-chr6:13677578..13681816,6	K562	blood:
31	chr6:13649255..13650817-chr6:13651728..13653387,2	K562	blood:
32	chr6:13634378..13636640-chr6:13639918..13642651,2	MCF-7	breast:
33	chr6:13644681..13646353-chr6:13651574..13653545,2	K562	blood:
34	chr6:13615461..13617321-chr6:13644402..13646054,2	MCF-7	breast:
35	chr6:13649360..13652106-chr6:13653582..13655129,2	K562	blood:
36	chr6:13613832..13619754-chr6:13637081..13641354,6	K562	blood:
37	chr6:13644315..13646666-chr6:13651574..13655085,5	K562	blood:
38	chr6:13687550..13689882-chr6:13710017..13712111,2	MCF-7	breast:
39	chr6:13624060..13626610-chr6:13660365..13663120,2	MCF-7	breast:
40	chr6:13642074..13646746-chr6:13710307..13713683,4	K562	blood:
41	chr6:13688886..13690711-chr6:13696299..13698751,3	K562	blood:
42	chr6:13659651..13661542-chr6:13715805..13717920,2	MCF-7	breast:
43	chr6:13678229..13680243-chr6:13687121..13689516,2	MCF-7	breast:
44	chr6:13633178..13635073-chr6:13648017..13650938,2	MCF-7	breast:
45	chr6:13654390..13656114-chr6:13661892..13663591,2	MCF-7	breast:
46	chr6:13634147..13636935-chr6:13665092..13667757,2	K562	blood:
47	chr6:13651312..13653506-chr6:13655143..13656683,2	K562	blood:
48	chr6:13654390..13656114-chr6:13661892..13663591,2	MCF-7	breast:
49	chr6:13657137..13658911-chr6:13667084..13669198,2	MCF-7	breast:
50	chr6:13653800..13655519-chr6:13709705..13714019,3	K562	blood:

No data

Variant related genes	Relation type
RNU7-91P	TF binding region
RANBP9	TF binding region
RNU7-91P	CpG island
RANBP9	CpG island
ENSG00000124523	chromatin interactions
ENSG00000261071	chromatin interactions
ENSG00000050393	chromatin interactions
ENSG00000225921	chromatin interactions
ENSG00000252966	chromatin interactions
ENSG00000010017	chromatin interactions

Extended variants
information (count: 2091 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:2091 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372510479	chr6:13634669-13634670	Enhancers Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs146194250	chr6:13634688-13634689	Enhancers Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs202203748	chr6:13634690-13634691	Enhancers Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs367985881	chr6:13634725-13634726	Enhancers Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs551528918	chr6:13634732-13634733	Enhancers Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs565262097	chr6:13634778-13634779	Enhancers Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs527966615	chr6:13634850-13634851	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs367846216	chr6:13634870-13634871	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs567552120	chr6:13634952-13634953	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs370568601	chr6:13634954-13634955	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs550017708	chr6:13634955-13634956	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs570101774	chr6:13634956-13634957	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs707816	chr6:13634982-13634983	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs183337867	chr6:13634989-13634990	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs569130474	chr6:13634996-13634997	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs147080671	chr6:13635062-13635063	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs534077530	chr6:13635072-13635073	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs531625680	chr6:13635108-13635109	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs145799789	chr6:13635111-13635112	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs138572259	chr6:13635118-13635119	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs542572297	chr6:13635119-13635120	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs187878597	chr6:13635143-13635144	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs149636720	chr6:13635246-13635247	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs193160135	chr6:13635269-13635270	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs548068242	chr6:13635286-13635287	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs79126916	chr6:13635304-13635305	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs183289247	chr6:13635325-13635326	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs187339181	chr6:13635398-13635399	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs561587639	chr6:13635408-13635409	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs143901366	chr6:13635507-13635508	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs550121499	chr6:13635569-13635570	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs141127812	chr6:13635578-13635579	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs575252974	chr6:13635629-13635630	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs532642702	chr6:13635637-13635638	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs376251977	chr6:13635649-13635650	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs192693670	chr6:13635692-13635693	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs571469083	chr6:13635695-13635696	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs56167238	chr6:13635717-13635718	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs371696453	chr6:13635719-13635720	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs141214665	chr6:13635731-13635732	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs567522149	chr6:13635760-13635761	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs535894043	chr6:13635762-13635763	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs556106057	chr6:13635766-13635767	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs529560204	chr6:13635804-13635805	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs556245248	chr6:13635805-13635806	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs375014067	chr6:13635808-13635809	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs184625897	chr6:13635826-13635827	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs544704350	chr6:13635841-13635842	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs139165261	chr6:13635849-13635850	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs530597074	chr6:13635850-13635851	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
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
Myelodysplastic syndrome	21251322	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
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	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
small cell lung cancer	20016488	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
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
abnormal development	18461090	CNVD
Cancer	16790693	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1725 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13616600-13637400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:13617200-13634800	Strong transcription	HUES64 Cell Line	embryonic stem cell
3	chr6:13617200-13634800	Strong transcription	Fetal Intestine Large	intestine
4	chr6:13617200-13638800	Weak transcription	Aorta	Aorta
5	chr6:13617400-13636400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr6:13617600-13634800	Strong transcription	Primary T cells from cord blood	blood
7	chr6:13617600-13635400	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr6:13617600-13642200	Strong transcription	Fetal Thymus	thymus
9	chr6:13617600-13642200	Strong transcription	HSMM	muscle
10	chr6:13617600-13642400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr6:13617800-13634800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr6:13617800-13638400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr6:13618000-13634800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
14	chr6:13618000-13634800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:13618000-13635400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr6:13618000-13641200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr6:13618000-13644200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr6:13618200-13635400	Strong transcription	Primary T cells fromperipheralblood	blood
19	chr6:13618200-13641800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr6:13618200-13644400	Strong transcription	K562	blood
21	chr6:13618200-13661200	Weak transcription	Fetal Brain Male	brain
22	chr6:13620000-13647200	Strong transcription	Dnd41	blood
23	chr6:13620000-13649600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:13620400-13660400	Weak transcription	Pancreas	Pancrea
25	chr6:13620600-13691000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr6:13622200-13636200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr6:13622200-13641600	Weak transcription	Right Ventricle	heart
28	chr6:13622800-13635200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr6:13622800-13637600	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr6:13622800-13638800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr6:13622800-13640800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr6:13623600-13637600	Weak transcription	Brain Substantia Nigra	brain
33	chr6:13623600-13656200	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr6:13625200-13638400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr6:13625200-13638600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr6:13625200-13638600	Weak transcription	Fetal Intestine Small	intestine
37	chr6:13625400-13660400	Weak transcription	Gastric	stomach
38	chr6:13625600-13637600	Weak transcription	NHLF	lung
39	chr6:13625600-13642600	Weak transcription	A549	lung
40	chr6:13626000-13660400	Weak transcription	Lung	lung
41	chr6:13626600-13637800	Weak transcription	Ovary	ovary
42	chr6:13626600-13667800	Weak transcription	Brain Cingulate Gyrus	brain
43	chr6:13626800-13637800	Weak transcription	Colonic Mucosa	Colon
44	chr6:13626800-13669000	Weak transcription	Brain Anterior Caudate	brain
45	chr6:13627200-13637600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr6:13628600-13634800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr6:13629000-13634800	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr6:13629400-13634800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr6:13630200-13636200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:13630400-13638400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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