Variant report

Variant	nsv933544
Chromosome Location	chr10:27005220-27111998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1340)
CpG islands
(count:427)
Chromatin interactive
region (count:83)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1340 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:27015086-27015416	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:27044346-27044879	K562	blood:	n/a	n/a
3	ARID3A	chr10:27099384-27099666	K562	blood:	n/a	n/a
4	ARID3A	chr10:27040028-27040039	K562	blood:	n/a	n/a
5	ARID3A	chr10:27086254-27086608	K562	blood:	n/a	n/a
6	ARID3A	chr10:27022975-27023447	HepG2	liver:	n/a	n/a
7	ATF1	chr10:27059156-27059158	K562	blood:	n/a	n/a
8	ATF1	chr10:27058589-27058781	K562	blood:	n/a	n/a
9	ATF2	chr10:27026583-27027221	GM12878	blood:	n/a	n/a
10	ATF2	chr10:27044275-27044979	GM12878	blood:	n/a	n/a
11	ATF2	chr10:27026110-27026462	GM12878	blood:	n/a	n/a
12	ATF2	chr10:27026508-27027449	GM12878	blood:	n/a	n/a
13	ATF2	chr10:27088195-27088724	GM12878	blood:	n/a	n/a
14	ATF2	chr10:27079416-27079766	GM12878	blood:	n/a	n/a
15	ATF2	chr10:27044369-27044915	GM12878	blood:	n/a	n/a
16	ATF3	chr10:27044324-27044683	K562	blood:	n/a	n/a
17	BACH1	chr10:27044381-27044755	H1-hESC	embryonic stem cell:	n/a	chr10:27044506-27044520
18	BACH1	chr10:27047917-27048291	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr10:27015297-27015497	K562	blood:	n/a	n/a
20	BACH1	chr10:27099345-27099709	K562	blood:	n/a	n/a
21	BATF	chr10:27088320-27088563	GM12878	blood:	n/a	n/a
22	BATF	chr10:27026708-27027072	GM12878	blood:	n/a	n/a
23	BATF	chr10:27026672-27027040	GM12878	blood:	n/a	n/a
24	BATF	chr10:27095579-27095863	GM12878	blood:	n/a	chr10:27095697-27095708
25	BATF	chr10:27044384-27044898	GM12878	blood:	n/a	n/a
26	BATF	chr10:27029086-27029326	GM12878	blood:	n/a	n/a
27	BATF	chr10:27026078-27026455	GM12878	blood:	n/a	n/a
28	BATF	chr10:27069978-27070519	GM12878	blood:	n/a	n/a
29	BATF	chr10:27029054-27029415	GM12878	blood:	n/a	n/a
30	BATF	chr10:27026030-27026343	GM12878	blood:	n/a	n/a
31	BATF	chr10:27072771-27073010	GM12878	blood:	n/a	chr10:27072862-27072873
32	BCL11A	chr10:27088278-27088601	GM12878	blood:	n/a	n/a
33	BCL11A	chr10:27026590-27027034	GM12878	blood:	n/a	chr10:27026758-27026767 chr10:27026884-27026893
34	BCL3	chr10:27026662-27027046	GM12878	blood:	n/a	chr10:27026758-27026767 chr10:27026884-27026893
35	BCL3	chr10:27031967-27032357	GM12878	blood:	n/a	n/a
36	BCL3	chr10:27026600-27027051	GM12878	blood:	n/a	chr10:27026758-27026767 chr10:27026884-27026893
37	BCLAF1	chr10:27088241-27088643	GM12878	blood:	n/a	n/a
38	BCLAF1	chr10:27026500-27027494	GM12878	blood:	n/a	chr10:27026758-27026767 chr10:27026884-27026893
39	BCLAF1	chr10:27044458-27044900	GM12878	blood:	n/a	chr10:27044509-27044518 chr10:27044508-27044517
40	BCLAF1	chr10:27025917-27026410	GM12878	blood:	n/a	n/a
41	BCLAF1	chr10:27026545-27027357	GM12878	blood:	n/a	chr10:27026758-27026767 chr10:27026884-27026893
42	BCLAF1	chr10:27028968-27029476	GM12878	blood:	n/a	n/a
43	BHLHE40	chr10:27088354-27088486	K562	blood:	n/a	n/a
44	BHLHE40	chr10:27044452-27044855	GM12878	blood:	n/a	n/a
45	BHLHE40	chr10:27026596-27027193	GM12878	blood:	n/a	n/a
46	BHLHE40	chr10:27089010-27089036	GM12878	blood:	n/a	n/a
47	BHLHE40	chr10:27015064-27015371	GM12878	blood:	n/a	n/a
48	BHLHE40	chr10:27023003-27023487	HepG2	liver:	n/a	n/a
49	BHLHE40	chr10:27099378-27099630	K562	blood:	n/a	n/a
50	BHLHE40	chr10:27088206-27088666	GM12878	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27059746-27059796	GM06990	blood:	n/a
2	chr10:27032461-27032511	ProgFib	skin:	n/a
3	chr10:27070113-27070163	LNCaP	prostate:	n/a
4	chr10:27023190-27023240	AoSMC	blood vessel:	n/a
5	chr10:27093175-27093225	GM12892	blood:	n/a
6	chr10:27044605-27044655	SK-N-MC	brain:	n/a
7	chr10:27032461-27032511	AG04449	skin:	fetal
8	chr10:27070113-27070163	Hela-S3	cervix:	n/a
9	chr10:27070113-27070163	NHDF-neo	bronchial:	n/a
10	chr10:27059746-27059796	HMEC	breast:	n/a
11	chr10:27059746-27059796	MCF-7	breast:	n/a
12	chr10:27070113-27070163	ProgFib	skin:	n/a
13	chr10:27044605-27044655	NB4	blood:	n/a
14	chr10:27070113-27070163	Hepatocyte	liver:	n/a
15	chr10:27032461-27032511	ECC-1	luminal epithelium:	n/a
16	chr10:27023190-27023240	NT2-D1	testis:	n/a
17	chr10:27059746-27059796	HEEpiC	esophagus:	n/a
18	chr10:27044605-27044655	Caco-2	colon:	n/a
19	chr10:27093175-27093225	PrEC	prostate:	n/a
20	chr10:27044605-27044655	AG09319	gingival:	n/a
21	chr10:27044605-27044655	ECC-1	luminal epithelium:	n/a
22	chr10:27093175-27093225	NHDF-neo	bronchial:	n/a
23	chr10:27093175-27093225	AG10803	skin:	n/a
24	chr10:27095369-27095419	AoSMC	blood vessel:	n/a
25	chr10:27044605-27044655	GM12892	blood:	n/a
26	chr10:27095369-27095419	HRCEpiC	kidney:	n/a
27	chr10:27070113-27070163	HEEpiC	esophagus:	n/a
28	chr10:27044605-27044655	K562	blood:	n/a
29	chr10:27093175-27093225	GM19239	blood:	n/a
30	chr10:27059746-27059796	Hepatocyte	liver:	n/a
31	chr10:27070113-27070163	ovcar-3	ovarian:	n/a
32	chr10:27032461-27032511	Caco-2	colon:	n/a
33	chr10:27023190-27023240	HCF	heart:	n/a
34	chr10:27023190-27023240	H1-hESC	embryonic stem cell:	embryo
35	chr10:27093175-27093225	NH-A	brain:	n/a
36	chr10:27070113-27070163	HUVEC	blood vessel:	n/a
37	chr10:27095369-27095419	PrEC	prostate:	n/a
38	chr10:27095369-27095419	NHDF-neo	bronchial:	n/a
39	chr10:27023190-27023240	AG04450	lung:	fetal
40	chr10:27070113-27070163	AG04449	skin:	fetal
41	chr10:27093175-27093225	HCM	heart:	n/a
42	chr10:27095369-27095419	HL-60	blood:	n/a
43	chr10:27093175-27093225	Hela-S3	cervix:	n/a
44	chr10:27059746-27059796	AG09319	gingival:	n/a
45	chr10:27070113-27070163	NHBE	bronchial:	n/a
46	chr10:27044605-27044655	MCF10A-Er-Src	breast:	n/a
47	chr10:27023190-27023240	HEEpiC	esophagus:	n/a
48	chr10:27032461-27032511	HPAEpiC	pulmonary alveolar:	n/a
49	chr10:27093175-27093225	GM06990	blood:	n/a
50	chr10:27070113-27070163	GM06990	blood:	n/a

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:27093725..27095601-chr10:27102289..27104640,2	MCF-7	breast:
2	chr10:27057922..27061577-chr10:27062885..27066099,3	K562	blood:
3	chr10:27021769..27024487-chr10:27025827..27029432,3	MCF-7	breast:
4	chr10:27066132..27067920-chr10:27074183..27076184,2	K562	blood:
5	chr10:27050329..27053574-chr10:27053805..27057713,4	K562	blood:
6	chr10:27050958..27053361-chr10:27064664..27066891,2	K562	blood:
7	chr10:27066132..27067920-chr10:27074183..27076184,2	K562	blood:
8	chr10:27014360..27015711-chr10:27170641..27171581,4	K562	blood:
9	chr10:27025829..27027714-chr10:27034224..27036690,2	K562	blood:
10	chr10:27036002..27038696-chr10:27039416..27041996,4	K562	blood:
11	chr10:27089103..27090816-chr10:27092531..27095480,2	K562	blood:
12	chr10:27002629..27005030-chr10:27030219..27032691,2	K562	blood:
13	chr10:27093725..27095601-chr10:27102289..27104640,2	MCF-7	breast:
14	chr10:27038672..27041354-chr10:27047222..27050106,2	K562	blood:
15	chr10:27034198..27037050-chr10:27043769..27046738,3	K562	blood:
16	chr10:27068463..27071008-chr10:27149449..27152029,3	K562	blood:
17	chr10:27087122..27088975-chr10:27089037..27091906,2	MCF-7	breast:
18	chr10:27067079..27070597-chr10:27072640..27074844,4	K562	blood:
19	chr10:26995580..26998397-chr10:27011031..27013187,2	K562	blood:
20	chr10:27070974..27073894-chr10:27148134..27150716,3	MCF-7	breast:
21	chr10:27025829..27027714-chr10:27034224..27036690,2	K562	blood:
22	chr10:27073078..27074935-chr10:27148333..27150643,2	K562	blood:
23	chr10:27087122..27088975-chr10:27089037..27091906,2	MCF-7	breast:
24	chr10:27074245..27076242-chr10:27078041..27079548,2	MCF-7	breast:
25	chr10:27106510..27108807-chr10:27111727..27113503,2	K562	blood:
26	chr10:27007355..27009512-chr10:27013703..27015717,2	K562	blood:
27	chr10:27045804..27047665-chr10:27149593..27151303,2	MCF-7	breast:
28	chr10:27028106..27031090-chr10:27040562..27042712,2	K562	blood:
29	chr10:26986123..26987914-chr10:27003670..27005754,2	MCF-7	breast:
30	chr10:27061393..27062937-chr10:27066179..27068006,2	MCF-7	breast:
31	chr10:27047313..27050355-chr10:27148384..27151067,3	K562	blood:
32	chr10:27051583..27054295-chr10:27088139..27090891,2	K562	blood:
33	chr10:27095663..27097538-chr10:27098853..27101729,2	K562	blood:
34	chr10:27054901..27057514-chr10:27069095..27071711,3	MCF-7	breast:
35	chr10:27050958..27053361-chr10:27064664..27066891,2	K562	blood:
36	chr10:27063322..27065877-chr10:27068617..27071382,2	K562	blood:
37	chr10:27037937..27039490-chr10:27047558..27049695,2	MCF-7	breast:
38	chr10:27067079..27070597-chr10:27072640..27074844,4	K562	blood:
39	chr10:27051583..27054295-chr10:27088139..27090891,2	K562	blood:
40	chr10:27009604..27012083-chr10:27443909..27445866,2	K562	blood:
41	chr10:27018097..27019836-chr10:27021900..27023987,2	K562	blood:
42	chr10:27015169..27015701-chr10:27150108..27150645,2	K562	blood:
43	chr10:27014809..27015628-chr10:27170414..27171655,4	MCF-7	breast:
44	chr10:27019861..27021992-chr10:27022425..27025039,2	K562	blood:
45	chr10:27020685..27022973-chr10:27138065..27140730,2	MCF-7	breast:
46	chr10:27020372..27021992-chr10:27022425..27024329,2	K562	blood:
47	chr10:27085060..27087648-chr10:27098555..27100631,2	K562	blood:
48	chr10:27095663..27097538-chr10:27098853..27101729,2	K562	blood:
49	chr10:27063322..27065877-chr10:27068617..27071382,2	K562	blood:
50	chr10:26985057..26986781-chr10:27006850..27009579,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDSS1-6	chr10:27084559-27085482	ncRnaDb_ncrna_FR197548_1
2	lnc-PDSS1-4	chr10:27044553-27045476	NONHSAT011861
3	lnc-APBB1IP-2	chr10:27006564-27007002	ENSG00000235843.1
4	lnc-APBB1IP-2	chr10:27007662-27007707	ENSG00000235843.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PDSS1	hsa-miR-320a	chr10:27035356-27035374
2	PDSS1	hsa-miR-98-5p	chr10:27035272-27035292

Variant related genes	Relation type
ENSG00000235843	TF binding region
ENSG00000223027	TF binding region
RNU6-946P	TF binding region
PDSS1	TF binding region
ENSG00000235843	CpG island
ENSG00000223027	CpG island
RNU6-946P	CpG island
PDSS1	CpG island
ENSG00000136754	chromatin interactions
ENSG00000234788	chromatin interactions
ENSG00000120539	chromatin interactions
ENSG00000136758	chromatin interactions
ENSG00000148459	chromatin interactions

Extended variants
information (count: 4004 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:4004 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373385034	chr10:27005229-27005230	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141315819	chr10:27005248-27005249	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs540904065	chr10:27005256-27005257	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs118181124	chr10:27005257-27005258	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs547928680	chr10:27005264-27005265	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs145491389	chr10:27005272-27005273	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs2489553	chr10:27005283-27005284	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs11015245	chr10:27005293-27005294	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs531668859	chr10:27005316-27005317	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs201811609	chr10:27005336-27005337	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs561712470	chr10:27005341-27005342	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs527701916	chr10:27005352-27005353	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs547621827	chr10:27005362-27005363	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs570646663	chr10:27005463-27005464	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs10764636	chr10:27005493-27005494	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs140940764	chr10:27005494-27005495	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs538148270	chr10:27005517-27005518	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs181286408	chr10:27005536-27005537	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs569901269	chr10:27005539-27005540	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs556481090	chr10:27005542-27005543	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs535511064	chr10:27005552-27005553	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs150184427	chr10:27005577-27005578	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551423719	chr10:27005620-27005621	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs74731804	chr10:27005621-27005622	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs138956740	chr10:27005626-27005627	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs140733572	chr10:27005628-27005629	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs145885658	chr10:27005630-27005631	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs138447131	chr10:27005632-27005633	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs540151003	chr10:27005636-27005637	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs556461757	chr10:27005642-27005643	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs576244027	chr10:27005674-27005675	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs377000928	chr10:27005675-27005676	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs552438180	chr10:27005706-27005707	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs571405932	chr10:27005707-27005708	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs368622805	chr10:27005709-27005710	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs79459336	chr10:27005747-27005748	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs142956043	chr10:27005833-27005834	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs11818967	chr10:27005836-27005837	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs114545599	chr10:27005884-27005885	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs371681224	chr10:27005931-27005932	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs201096944	chr10:27005985-27005986	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147996135	chr10:27005990-27005991	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373857674	chr10:27006065-27006066	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550066260	chr10:27006066-27006067	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141636145	chr10:27006067-27006068	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529107244	chr10:27006102-27006103	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549060375	chr10:27006134-27006135	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs371077615	chr10:27006137-27006138	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs142778708	chr10:27006160-27006161	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs75222700	chr10:27006176-27006177	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	22037309	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 myeloid leukemia	20824076	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3149 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26987600-27010400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr10:26987600-27024400	Weak transcription	Fetal Kidney	kidney
3	chr10:26987800-27010800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr10:26987800-27020400	Weak transcription	Primary hematopoietic stem cells	blood
5	chr10:26987800-27031200	Weak transcription	NHDF-Ad	bronchial
6	chr10:26988000-27069600	Weak transcription	Colon Smooth Muscle	Colon
7	chr10:26988200-27009600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr10:26988200-27009800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr10:26988400-27009800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr10:26989400-27031000	Weak transcription	Small Intestine	intestine
11	chr10:26994200-27007800	Strong transcription	Fetal Stomach	stomach
12	chr10:26994400-27007800	Strong transcription	Thymus	Thymus
13	chr10:26994400-27010600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr10:26994400-27040800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr10:26995400-27023000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr10:26995800-27026600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr10:26996000-27026600	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr10:26996200-27026200	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr10:26996200-27028000	Weak transcription	Psoas Muscle	Psoas
20	chr10:26996600-27012000	Weak transcription	Brain Cingulate Gyrus	brain
21	chr10:26996600-27022400	Weak transcription	Brain Angular Gyrus	brain
22	chr10:26996600-27023600	Weak transcription	Fetal Heart	heart
23	chr10:26996800-27010600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr10:26997200-27010000	Weak transcription	Pancreas	Pancrea
25	chr10:26997200-27012200	Weak transcription	HSMM	muscle
26	chr10:26997200-27022800	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr10:26997200-27024400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr10:26997400-27010600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr10:26997400-27022400	Weak transcription	Brain Substantia Nigra	brain
30	chr10:26997600-27005400	Weak transcription	HUVEC	blood vessel
31	chr10:26997600-27008800	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr10:26997600-27010400	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr10:26997600-27012800	Weak transcription	Brain Hippocampus Middle	brain
34	chr10:26997600-27054400	Weak transcription	Fetal Brain Male	brain
35	chr10:26998000-27005800	Weak transcription	NHLF	lung
36	chr10:26998000-27009800	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr10:26998000-27010800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr10:26998000-27011800	Weak transcription	Rectal Smooth Muscle	rectum
39	chr10:26998000-27022400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr10:26998200-27010600	Weak transcription	Esophagus	oesophagus
41	chr10:26998200-27015000	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr10:26998200-27015400	Weak transcription	Brain Anterior Caudate	brain
43	chr10:26998200-27022400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr10:26998600-27009400	Weak transcription	HSMMtube	muscle
45	chr10:26998600-27012200	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr10:26999000-27010600	Weak transcription	Lung	lung
47	chr10:26999800-27022600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
48	chr10:26999800-27037400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr10:27000600-27009000	Weak transcription	Right Ventricle	heart
50	chr10:27000800-27010400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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