Variant report

Variant	nsv1002358
Chromosome Location	chr2:148703807-148942372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1840)
CpG islands
(count:1099)
Chromatin interactive
region (count:98)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1840 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:148780420-148780619	K562	blood:	n/a	n/a
2	ARID3A	chr2:148777639-148778741	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:148779891-148780131	K562	blood:	n/a	n/a
4	ARID3A	chr2:148810230-148810584	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:148756715-148756858	K562	blood:	n/a	n/a
6	ARID3A	chr2:148888294-148888308	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:148747414-148747709	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:148778946-148779315	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:148920439-148920729	K562	blood:	n/a	n/a
10	ARID3A	chr2:148777693-148778271	K562	blood:	n/a	n/a
11	ARID3A	chr2:148776453-148776679	K562	blood:	n/a	n/a
12	ARID3A	chr2:148747394-148747852	K562	blood:	n/a	n/a
13	ATF1	chr2:148778210-148778730	K562	blood:	n/a	n/a
14	ATF2	chr2:148777775-148778557	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr2:148799610-148800244	GM12878	blood:	n/a	n/a
16	ATF2	chr2:148799549-148800235	GM12878	blood:	n/a	n/a
17	ATF2	chr2:148805695-148807140	GM12878	blood:	n/a	n/a
18	ATF2	chr2:148805766-148807114	GM12878	blood:	n/a	n/a
19	ATF2	chr2:148777599-148779168	GM12878	blood:	n/a	n/a
20	ATF2	chr2:148778167-148779037	GM12878	blood:	n/a	n/a
21	ATF3	chr2:148777950-148778529	GM12878	blood:	n/a	chr2:148778471-148778480
22	ATF3	chr2:148778167-148778529	HepG2	liver:	n/a	chr2:148778471-148778480
23	BACH1	chr2:148936476-148936481	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr2:148789167-148789394	GM12878	blood:	n/a	n/a
25	BATF	chr2:148880380-148880646	GM12878	blood:	n/a	chr2:148880539-148880550
26	BATF	chr2:148799772-148800076	GM12878	blood:	n/a	chr2:148799907-148799918
27	BATF	chr2:148803918-148804156	GM12878	blood:	n/a	n/a
28	BATF	chr2:148806449-148806848	GM12878	blood:	n/a	chr2:148806614-148806625
29	BATF	chr2:148803827-148804138	GM12878	blood:	n/a	n/a
30	BATF	chr2:148799707-148800070	GM12878	blood:	n/a	chr2:148799907-148799918
31	BATF	chr2:148806259-148806907	GM12878	blood:	n/a	chr2:148806614-148806625
32	BCL11A	chr2:148799776-148800128	GM12878	blood:	n/a	chr2:148800002-148800011
33	BCL11A	chr2:148799845-148800073	GM12878	blood:	n/a	chr2:148800002-148800011
34	BCL11A	chr2:148806525-148806767	GM12878	blood:	n/a	n/a
35	BCL11A	chr2:148806110-148806885	GM12878	blood:	n/a	n/a
36	BCL3	chr2:148799732-148800218	GM12878	blood:	n/a	chr2:148800002-148800011
37	BCL3	chr2:148805871-148806863	GM12878	blood:	n/a	n/a
38	BCL3	chr2:148778097-148778782	A549	lung:	n/a	chr2:148778394-148778403
39	BCLAF1	chr2:148777882-148779142	GM12878	blood:	n/a	chr2:148778394-148778403
40	BCLAF1	chr2:148799725-148800084	GM12878	blood:	n/a	chr2:148800002-148800011
41	BCLAF1	chr2:148799581-148800151	GM12878	blood:	n/a	chr2:148800002-148800011
42	BCLAF1	chr2:148806074-148806967	GM12878	blood:	n/a	n/a
43	BCLAF1	chr2:148747364-148747810	GM12878	blood:	n/a	n/a
44	BCLAF1	chr2:148805628-148807044	GM12878	blood:	n/a	n/a
45	BCLAF1	chr2:148778798-148779291	GM12878	blood:	n/a	n/a
46	BCLAF1	chr2:148777838-148778752	GM12878	blood:	n/a	chr2:148778394-148778403
47	BHLHE40	chr2:148842666-148842699	A549	lung:	n/a	n/a
48	BHLHE40	chr2:148783631-148783811	K562	blood:	n/a	n/a
49	BHLHE40	chr2:148805899-148807141	GM12878	blood:	n/a	n/a
50	BHLHE40	chr2:148747431-148747876	GM12878	blood:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:148778181-148778231	PrEC	prostate:	n/a
2	chr2:148778181-148778231	PrEC	prostate:	n/a
3	chr2:148815999-148816049	T-47D	breast:	n/a
4	chr2:148777915-148777965	Jurkat	blood:	n/a
5	chr2:148839265-148839315	HCF	heart:	n/a
6	chr2:148778181-148778231	U87	brain:	n/a
7	chr2:148839265-148839315	RPTEC	kidney:	n/a
8	chr2:148779564-148779614	HNPCEpiC	eye:	n/a
9	chr2:148782427-148782477	GM06990	blood:	n/a
10	chr2:148779335-148779385	A549	lung:	n/a
11	chr2:148779683-148779733	HL-60	blood:	n/a
12	chr2:148779335-148779385	PrEC	prostate:	n/a
13	chr2:148779307-148779357	SK-N-SH	brain:	n/a
14	chr2:148893152-148893202	HepG2	liver:	n/a
15	chr2:148779307-148779357	CMK	blood:	n/a
16	chr2:148747824-148747874	NB4	blood:	n/a
17	chr2:148839265-148839315	NH-A	brain:	n/a
18	chr2:148778969-148779019	HRCEpiC	kidney:	n/a
19	chr2:148779564-148779614	HCPEpiC	choroid plexus:	n/a
20	chr2:148747824-148747874	MCF10A-Er-Src	breast:	n/a
21	chr2:148779683-148779733	HRCEpiC	kidney:	n/a
22	chr2:148779683-148779733	A549	lung:	n/a
23	chr2:148782427-148782477	HCT-116	colon:	n/a
24	chr2:148778181-148778231	RPTEC	kidney:	n/a
25	chr2:148753294-148753344	HAEpiC	amniotic membrane:	n/a
26	chr2:148778969-148779019	NH-A	brain:	n/a
27	chr2:148782427-148782477	HCPEpiC	choroid plexus:	n/a
28	chr2:148779348-148779398	LNCaP	prostate:	n/a
29	chr2:148815999-148816049	AG09319	gingival:	n/a
30	chr2:148779683-148779733	T-47D	breast:	n/a
31	chr2:148782427-148782477	AG10803	skin:	n/a
32	chr2:148778288-148778338	NHBE	bronchial:	n/a
33	chr2:148779335-148779385	GM19239	blood:	n/a
34	chr2:148839265-148839315	SK-N-MC	brain:	n/a
35	chr2:148893152-148893202	GM12878	blood:	n/a
36	chr2:148758708-148758758	T-47D	breast:	n/a
37	chr2:148753294-148753344	AG09319	gingival:	n/a
38	chr2:148779335-148779385	NHDF-neo	bronchial:	n/a
39	chr2:148778495-148778545	BE2_C	brain:	n/a
40	chr2:148779683-148779733	HCF	heart:	n/a
41	chr2:148778495-148778545	HAEpiC	amniotic membrane:	n/a
42	chr2:148779335-148779385	HRPEpiC	eye:	n/a
43	chr2:148815999-148816049	HMEC	breast:	n/a
44	chr2:148839265-148839315	HL-60	blood:	n/a
45	chr2:148753294-148753344	Caco-2	colon:	n/a
46	chr2:148753294-148753344	SKMC	muscle:	n/a
47	chr2:148732064-148732114	NHBE	bronchial:	n/a
48	chr2:148753294-148753344	IMR90	lung:	fetal
49	chr2:148778181-148778231	PANC-1	pancreas:	n/a
50	chr2:148779307-148779357	HCT-116	colon:	n/a

(count:98 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:148755309..148758512-chr2:148776445..148778931,3	MCF-7	breast:
2	chr2:148831814..148833866-chr2:148838337..148840088,2	K562	blood:
3	chr2:148717126..148719327-chr2:148720012..148722132,2	K562	blood:
4	chr2:148747289..148748018-chr2:149266484..149267635,9	MCF-7	breast:
5	chr2:148762250..148764768-chr2:148777590..148779447,2	MCF-7	breast:
6	chr2:148892318..148894319-chr2:148896559..148898244,2	MCF-7	breast:
7	chr2:148801657..148804409-chr2:148807658..148809416,2	MCF-7	breast:
8	chr2:148722716..148725522-chr2:148725582..148727272,2	MCF-7	breast:
9	chr2:148765519..148769720-chr2:148770172..148772833,3	K562	blood:
10	chr2:148931889..148933794-chr2:148936353..148939104,2	K562	blood:
11	chr2:148862754..148865628-chr2:148893706..148895344,2	K562	blood:
12	chr2:148796353..148798191-chr2:148802415..148804582,2	K562	blood:
13	chr2:148790035..148791910-chr2:148820838..148823392,2	K562	blood:
14	chr2:148777791..148778435-chr9:34611815..34612562,2	NB4	blood:
15	chr2:148869849..148872323-chr2:148885274..148887437,2	MCF-7	breast:
16	chr2:148839523..148841211-chr2:148842127..148844445,2	K562	blood:
17	chr2:148839523..148841211-chr2:148842127..148844445,2	K562	blood:
18	chr2:148777810..148780521-chr2:149401501..149403816,2	MCF-7	breast:
19	chr2:148704147..148707130-chr2:149248171..149249711,2	K562	blood:
20	chr2:148765021..148767403-chr2:148770633..148772597,2	K562	blood:
21	chr2:148794522..148796703-chr2:148799769..148801375,2	K562	blood:
22	chr14:31090963..31091593-chr2:148777702..148778439,2	Hela-S3	cervix:
23	chr2:148795246..148798191-chr2:148802393..148803915,2	K562	blood:
24	chr2:148888593..148891096-chr2:148894086..148896797,2	K562	blood:
25	chr2:148772919..148776158-chr2:148776634..148779455,3	MCF-7	breast:
26	chr2:148790035..148791910-chr2:148820838..148823392,2	K562	blood:
27	chr2:148862754..148865628-chr2:148893706..148895344,2	K562	blood:
28	chr2:148732231..148734888-chr2:148736487..148738854,2	K562	blood:
29	chr2:148736461..148738004-chr2:148741042..148743532,2	K562	blood:
30	chr2:148746863..148748075-chr2:149266691..149267630,3	K562	blood:
31	chr2:148784396..148788846-chr2:148789085..148797042,12	K562	blood:
32	chr2:148782652..148784833-chr2:148785431..148787188,2	MCF-7	breast:
33	chr2:148892318..148894319-chr2:148896559..148898244,2	MCF-7	breast:
34	chr2:148826768..148827504-chr6:20350150..20350710,2	MCF-7	breast:
35	chr2:148747119..148747979-chr2:148777459..148778023,2	MCF-7	breast:
36	chr2:148777185..148777981-chr2:149266660..149267608,2	MCF-7	breast:
37	chr2:148857706..148860074-chr2:148877712..148879777,2	K562	blood:
38	chr2:148747741..148748520-chr2:149322760..149323458,2	K562	blood:
39	chr2:148766857..148769068-chr2:148777403..148779388,2	K562	blood:
40	chr1:145382244..145383020-chr2:148777927..148778778,2	HCT-116	colon:
41	chr2:148793989..148796591-chr2:148815417..148817298,2	K562	blood:
42	chr2:148884069..148886701-chr2:148890123..148892046,2	MCF-7	breast:
43	chr2:148784529..148787318-chr2:148787850..148789462,2	MCF-7	breast:
44	chr2:148736461..148738004-chr2:148741042..148743532,2	K562	blood:
45	chr2:148793989..148796591-chr2:148815417..148817298,2	K562	blood:
46	chr2:148811506..148813577-chr2:148817603..148819976,2	K562	blood:
47	chr2:148796353..148798191-chr2:148802415..148804582,2	K562	blood:
48	chr2:148778014..148780334-chr2:148791954..148794463,2	K562	blood:
49	chr2:148784529..148787318-chr2:148787850..148789462,2	MCF-7	breast:
50	chr2:148924504..148926944-chr2:148937289..148939887,2	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074875
2	lnc-MBD5-1	chr2:148779033-148779253	NONHSAT074875
3	lnc-MBD5-1	chr2:148782535-148782771	NONHSAT074877
4	lnc-MMADHC-10	chr2:148733471-148733544	NONHSAT074870
5	lnc-MMADHC-10	chr2:148731017-148731093	NONHSAT074870
6	lnc-MBD5-1	chr2:148778596-148778615	NONHSAT074872
7	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074878
8	lnc-MBD5-1	chr2:148778807-148779253	NONHSAT074873
9	lnc-MBD5-1	chr2:148779008-148779253	NONHSAT074874
10	lnc-MBD5-1	chr2:148782535-148782627	NONHSAT074873
11	lnc-MBD5-1	chr2:148826141-148826162	NONHSAT074878
12	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074874
13	lnc-MBD5-1	chr2:148779162-148779253	NONHSAT074876
14	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074872
15	lnc-MBD5-1	chr2:148798775-148798934	NONHSAT074876
16	lnc-MBD5-1	chr2:148778580-148778615	NONHSAT074871
17	lnc-MMADHC-10	chr2:148716161-148716435	NONHSAT074870
18	lnc-MMADHC-10	chr2:148730308-148730398	NONHSAT074870
19	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074871
20	lnc-MMADHC-10	chr2:148778202-148778295	NONHSAT074870
21	lnc-MBD5-1	chr2:148781621-148781743	NONHSAT074877
22	lnc-MBD5-1	chr2:148811960-148812018	NONHSAT074874

No data

Variant related genes	Relation type
ORC4	TF binding region
MBD5	TF binding region
ORC4	CpG island
MBD5	CpG island
ENSG00000151876	chromatin interactions
ENSG00000092108	chromatin interactions
ENSG00000204406	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000164967	chromatin interactions
ENSG00000115947	chromatin interactions
ENSG00000168394	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000135999	chromatin interactions

Extended variants
information (count: 8004 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:8004 , 50 per page) page: 1 2 3 4 5 6 7 ... 161

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200443156	chr2:148703862-148703863	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs544082233	chr2:148703864-148703865	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143757316	chr2:148703865-148703866	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs200391258	chr2:148703874-148703875	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551368225	chr2:148703899-148703900	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs562996633	chr2:148703906-148703907	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs372316305	chr2:148703917-148703918	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs549952033	chr2:148703918-148703919	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568347063	chr2:148703946-148703947	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs3768684	chr2:148703965-148703966	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs74362961	chr2:148703978-148703979	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs370488497	chr2:148704017-148704018	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs566377435	chr2:148704067-148704068	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs539406746	chr2:148704091-148704092	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs553059318	chr2:148704160-148704161	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574443291	chr2:148704186-148704187	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs558231932	chr2:148704226-148704227	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs576604314	chr2:148704269-148704270	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs372593825	chr2:148704321-148704322	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs202183500	chr2:148704327-148704328	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs529674901	chr2:148704392-148704393	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs145515706	chr2:148704432-148704433	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs535679498	chr2:148704456-148704457	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs148840222	chr2:148704464-148704465	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs556884200	chr2:148704500-148704501	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs541237097	chr2:148704522-148704523	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546526726	chr2:148704539-148704540	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs559347025	chr2:148704578-148704579	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs577871354	chr2:148704582-148704583	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs1227305	chr2:148704616-148704617	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs545717271	chr2:148704637-148704638	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs113744896	chr2:148704658-148704659	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs187019242	chr2:148704667-148704668	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs530507155	chr2:148704715-148704716	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs10460259	chr2:148704721-148704722	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs560669104	chr2:148704722-148704723	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs576863596	chr2:148704728-148704729	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs113971257	chr2:148704733-148704734	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs547976605	chr2:148704773-148704774	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs566242466	chr2:148704849-148704850	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs191116859	chr2:148704853-148704854	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs183380489	chr2:148704906-148704907	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs143494372	chr2:148704908-148704909	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs1030317	chr2:148704932-148704933	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs551334175	chr2:148704944-148704945	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs17231966	chr2:148704979-148704980	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs148152911	chr2:148704980-148704981	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs572964266	chr2:148705016-148705017	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs186636773	chr2:148705035-148705036	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs142936317	chr2:148705066-148705067	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	19904302	CNVD
Intellectual disability	19904302	CNVD
Microcephaly	19904302	CNVD
severe speech impairment	19904302	CNVD
Mental retardation	20152051	CNVD
2q23.1 microdeletion syndrome	18812405	CNVD
Mental retardation	19809484	CNVD
Autism	21981781	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Mental retardation	17847001	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20531469	CNVD

Chromatin state (count:3097 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:148637200-148752600	Weak transcription	Small Intestine	intestine
2	chr2:148647200-148719600	Weak transcription	Pancreas	Pancrea
3	chr2:148650200-148719600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:148653200-148719600	Weak transcription	Esophagus	oesophagus
5	chr2:148658800-148741600	Weak transcription	Aorta	Aorta
6	chr2:148659600-148719800	Weak transcription	Gastric	stomach
7	chr2:148661600-148718200	Weak transcription	Fetal Intestine Small	intestine
8	chr2:148664600-148721200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:148671800-148719600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr2:148672200-148706800	Weak transcription	Brain Germinal Matrix	brain
11	chr2:148675400-148708800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr2:148676200-148722400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr2:148678000-148718200	Weak transcription	Right Ventricle	heart
14	chr2:148679000-148718800	Weak transcription	Fetal Stomach	stomach
15	chr2:148679600-148737200	Weak transcription	Hela-S3	cervix
16	chr2:148681000-148729600	Weak transcription	NHDF-Ad	bronchial
17	chr2:148683000-148708400	Weak transcription	Rectal Smooth Muscle	rectum
18	chr2:148683000-148725200	Weak transcription	Fetal Heart	heart
19	chr2:148683200-148708800	Weak transcription	Psoas Muscle	Psoas
20	chr2:148685000-148707600	Weak transcription	Fetal Brain Male	brain
21	chr2:148685000-148708600	Weak transcription	Stomach Smooth Muscle	stomach
22	chr2:148685200-148707400	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr2:148688200-148719800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr2:148688200-148728600	Weak transcription	NH-A	brain
25	chr2:148688400-148707400	Weak transcription	Colon Smooth Muscle	Colon
26	chr2:148688800-148708600	Weak transcription	GM12878-XiMat	blood
27	chr2:148688800-148719600	Weak transcription	Thymus	Thymus
28	chr2:148689200-148708600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr2:148691000-148734600	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr2:148692000-148720200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr2:148692400-148713400	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr2:148692800-148719400	Weak transcription	HSMMtube	muscle
33	chr2:148693000-148712600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr2:148693400-148708400	Weak transcription	Fetal Lung	lung
35	chr2:148693400-148715600	Weak transcription	NHLF	lung
36	chr2:148693400-148722000	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr2:148693800-148724200	Weak transcription	Brain Hippocampus Middle	brain
38	chr2:148694000-148707800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr2:148694000-148708400	Weak transcription	Duodenum Mucosa	Duodenum
40	chr2:148694000-148708400	Weak transcription	HSMM	muscle
41	chr2:148694000-148708600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr2:148694000-148719600	Weak transcription	Fetal Brain Female	brain
43	chr2:148694000-148721000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr2:148694000-148725400	Weak transcription	Brain Anterior Caudate	brain
45	chr2:148694000-148731400	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr2:148694200-148706800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr2:148694200-148708800	Weak transcription	HMEC	breast
48	chr2:148694200-148708800	Weak transcription	HUVEC	blood vessel
49	chr2:148694200-148777400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr2:148694400-148708200	Weak transcription	Fetal Muscle Leg	muscle

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