Variant report

Variant	nsv916766
Chromosome Location	chr2:148743880-148955720
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1738)
CpG islands
(count:1039)
Chromatin interactive
region (count:88)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1738 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

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

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:148778495-148778545	Hela-S3	cervix:	n/a
2	chr2:148753294-148753344	NT2-D1	testis:	n/a
3	chr2:148778495-148778545	Hela-S3	cervix:	n/a
4	chr2:148753294-148753344	NT2-D1	testis:	n/a
5	chr2:148747824-148747874	Hepatocyte	liver:	n/a
6	chr2:148782427-148782477	HCM	heart:	n/a
7	chr2:148778288-148778338	T-47D	breast:	n/a
8	chr2:148779348-148779398	HepG2	liver:	n/a
9	chr2:148779564-148779614	NH-A	brain:	n/a
10	chr2:148839265-148839315	Hepatocyte	liver:	n/a
11	chr2:148779564-148779614	Jurkat	blood:	n/a
12	chr2:148779335-148779385	NT2-D1	testis:	n/a
13	chr2:148778969-148779019	AG04450	lung:	fetal
14	chr2:148893152-148893202	HCM	heart:	n/a
15	chr2:148779683-148779733	HUVEC	blood vessel:	n/a
16	chr2:148778969-148779019	SKMC	muscle:	n/a
17	chr2:148758708-148758758	HRPEpiC	eye:	n/a
18	chr2:148779335-148779385	Hepatocyte	liver:	n/a
19	chr2:148778288-148778338	BJ	skin:	n/a
20	chr2:148839265-148839315	NT2-D1	testis:	n/a
21	chr2:148777915-148777965	SAEC	small airway:	n/a
22	chr2:148758708-148758758	GM12891	blood:	n/a
23	chr2:148778495-148778545	HCT-116	colon:	n/a
24	chr2:148778495-148778545	SAEC	small airway:	n/a
25	chr2:148779564-148779614	HIPEpiC	eye:	n/a
26	chr2:148779335-148779385	Jurkat	blood:	n/a
27	chr2:148753294-148753344	U87	brain:	n/a
28	chr2:148815999-148816049	PrEC	prostate:	n/a
29	chr2:148753294-148753344	NHBE	bronchial:	n/a
30	chr2:148839265-148839315	AG04450	lung:	fetal
31	chr2:148779564-148779614	HL-60	blood:	n/a
32	chr2:148782427-148782477	HIPEpiC	eye:	n/a
33	chr2:148779348-148779398	AoSMC	blood vessel:	n/a
34	chr2:148753294-148753344	AG10803	skin:	n/a
35	chr2:148758708-148758758	MCF10A-Er-Src	breast:	n/a
36	chr2:148758708-148758758	T-47D	breast:	n/a
37	chr2:148747824-148747874	PANC-1	pancreas:	n/a
38	chr2:148758708-148758758	AG09309	skin:	n/a
39	chr2:148778969-148779019	T-47D	breast:	n/a
40	chr2:148777915-148777965	HUVEC	blood vessel:	n/a
41	chr2:148778969-148779019	H1-hESC	embryonic stem cell:	embryo
42	chr2:148778495-148778545	NHBE	bronchial:	n/a
43	chr2:148815999-148816049	LNCaP	prostate:	n/a
44	chr2:148777915-148777965	NB4	blood:	n/a
45	chr2:148782427-148782477	ECC-1	luminal epithelium:	n/a
46	chr2:148778969-148779019	HCM	heart:	n/a
47	chr2:148758708-148758758	HEEpiC	esophagus:	n/a
48	chr2:148779335-148779385	AG09309	skin:	n/a
49	chr2:148778969-148779019	LNCaP	prostate:	n/a
50	chr2:148779683-148779733	BE2_C	brain:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:148746863..148748075-chr2:149266691..149267630,3	K562	blood:
2	chr2:148859675..148863197-chr2:148868107..148869963,3	MCF-7	breast:
3	chr2:148811506..148813577-chr2:148817603..148819976,2	K562	blood:
4	chr2:148747119..148747979-chr2:148777459..148778023,2	MCF-7	breast:
5	chr2:148762432..148764977-chr2:148778675..148780305,2	MCF-7	breast:
6	chr2:148747741..148748520-chr2:149322760..149323458,2	K562	blood:
7	chr2:148747289..148748018-chr2:149266484..149267635,9	MCF-7	breast:
8	chr2:148765021..148767403-chr2:148770633..148772597,2	K562	blood:
9	chr2:148924504..148926944-chr2:148937289..148939887,2	MCF-7	breast:
10	chr2:148793989..148796591-chr2:148815417..148817298,2	K562	blood:
11	chr2:148766857..148769068-chr2:148777403..148779388,2	K562	blood:
12	chr2:148790987..148792533-chr2:148818638..148820263,2	K562	blood:
13	chr2:148796353..148798191-chr2:148802415..148804582,2	K562	blood:
14	chr2:148888593..148891096-chr2:148894086..148896797,2	K562	blood:
15	chr2:148884069..148886701-chr2:148890123..148892046,2	MCF-7	breast:
16	chr2:148839523..148841211-chr2:148842127..148844445,2	K562	blood:
17	chr2:148888593..148891096-chr2:148894086..148896797,2	K562	blood:
18	chr2:148777810..148780521-chr2:149401501..149403816,2	MCF-7	breast:
19	chr2:148892318..148894319-chr2:148896559..148898244,2	MCF-7	breast:
20	chr2:148869849..148872323-chr2:148885274..148887437,2	MCF-7	breast:
21	chr2:148747119..148747979-chr2:148777459..148778023,2	MCF-7	breast:
22	chr2:148801242..148804386-chr2:148805992..148808157,4	K562	blood:
23	chr2:148869849..148872323-chr2:148885274..148887437,2	MCF-7	breast:
24	chr2:148777791..148778435-chr9:34611815..34612562,2	NB4	blood:
25	chr2:148755309..148758512-chr2:148776445..148778931,3	MCF-7	breast:
26	chr2:148784396..148788846-chr2:148789085..148797042,12	K562	blood:
27	chr2:148852527..148854088-chr2:148860647..148862456,2	MCF-7	breast:
28	chr2:148765519..148769720-chr2:148770172..148772833,3	K562	blood:
29	chr2:148782652..148784833-chr2:148785431..148787188,2	MCF-7	breast:
30	chr2:148826768..148827504-chr6:20350150..20350710,2	MCF-7	breast:
31	chr2:148790987..148792533-chr2:148818638..148820263,2	K562	blood:
32	chr2:148795246..148798191-chr2:148802393..148803915,2	K562	blood:
33	chr2:148801657..148804409-chr2:148807658..148809416,2	MCF-7	breast:
34	chr2:148772919..148776158-chr2:148776634..148779455,3	MCF-7	breast:
35	chr2:148857706..148860074-chr2:148877712..148879777,2	K562	blood:
36	chr2:148801242..148804386-chr2:148805992..148808157,4	K562	blood:
37	chr2:148762250..148764768-chr2:148777590..148779447,2	MCF-7	breast:
38	chr2:148931889..148933794-chr2:148936353..148939104,2	K562	blood:
39	chr2:148747086..148748063-chr2:149266705..149267668,7	MCF-7	breast:
40	chr2:148862754..148865628-chr2:148893706..148895344,2	K562	blood:
41	chr2:148747393..148748097-chr2:149846190..149846982,2	MCF-7	breast:
42	chr2:148781884..148783998-chr2:148786718..148789864,3	K562	blood:
43	chr2:148773879..148776006-chr2:148779968..148781591,2	MCF-7	breast:
44	chr2:148778014..148780334-chr2:148791954..148794463,2	K562	blood:
45	chr2:148746466..148747928-chr2:148959011..148960040,7	MCF-7	breast:
46	chr2:148777400..148781221-chr2:148785788..148788815,4	MCF-7	breast:
47	chr2:148747178..148748066-chr2:148853587..148854325,3	MCF-7	breast:
48	chr2:148818705..148820589-chr2:148824017..148825657,2	MCF-7	breast:
49	chr2:148794522..148796703-chr2:148799769..148801375,2	K562	blood:
50	chr2:148884069..148886701-chr2:148890123..148892046,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 7065 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:7065 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546715943	chr2:148743960-148743961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs571406870	chr2:148744033-148744034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs79995232	chr2:148744073-148744074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191102133	chr2:148744076-148744077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570179414	chr2:148744106-148744107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143181126	chr2:148744124-148744125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2219145	chr2:148744149-148744150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557475193	chr2:148744258-148744259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115004792	chr2:148744313-148744314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567645071	chr2:148744331-148744332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201273404	chr2:148744355-148744356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs199628271	chr2:148744359-148744360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs71731628	chr2:148744360-148744361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs397986185	chr2:148744383-148744384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553031284	chr2:148744385-148744386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs767914	chr2:148744420-148744421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546371593	chr2:148744429-148744430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538768798	chr2:148744466-148744467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs200477175	chr2:148744526-148744527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79718107	chr2:148744617-148744618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs77336318	chr2:148744618-148744619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs557084456	chr2:148744632-148744633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575356511	chr2:148744670-148744671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564665481	chr2:148744704-148744705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542858979	chr2:148744727-148744728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561076785	chr2:148744746-148744747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11399347	chr2:148744755-148744756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs397770779	chr2:148744768-148744769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs6715174	chr2:148744809-148744810	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs540266351	chr2:148744832-148744833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555882184	chr2:148744842-148744843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369424632	chr2:148744843-148744844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141100317	chr2:148744858-148744859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532219681	chr2:148744866-148744867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183441832	chr2:148744889-148744890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550422569	chr2:148744891-148744892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150764325	chr2:148744926-148744927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368120116	chr2:148744935-148744936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200631420	chr2:148744936-148744937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs58302988	chr2:148744937-148744938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372437598	chr2:148744951-148744952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200791218	chr2:148744952-148744953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201483991	chr2:148744953-148744954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199752824	chr2:148744960-148744961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191115214	chr2:148744962-148744963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs202073386	chr2:148744981-148744982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73005159	chr2:148744982-148744983	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs370757347	chr2:148745073-148745074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376564302	chr2:148745079-148745080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531057003	chr2:148745138-148745139	Weak transcription	n/a	n/a	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:2314 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:148637200-148752600	Weak transcription	Small Intestine	intestine
2	chr2:148694200-148777400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr2:148695000-148746800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr2:148709200-148747600	Weak transcription	Adipose Nuclei	Adipose
5	chr2:148709400-148776800	Weak transcription	Stomach Smooth Muscle	stomach
6	chr2:148709800-148747000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:148721400-148752800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr2:148721400-148763600	Weak transcription	Spleen	Spleen
9	chr2:148722800-148756400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr2:148725600-148747600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr2:148726400-148752600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr2:148726600-148746800	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr2:148726600-148752600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr2:148728200-148773400	Weak transcription	K562	blood
15	chr2:148730800-148752600	Weak transcription	Primary T cells from cord blood	blood
16	chr2:148731000-148746200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr2:148731000-148746600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr2:148731000-148746800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr2:148731200-148746400	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr2:148731400-148752800	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr2:148736000-148776800	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr2:148736200-148744000	Weak transcription	Liver	Liver
23	chr2:148736200-148747000	Weak transcription	Left Ventricle	heart
24	chr2:148736200-148752000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr2:148736200-148752400	Weak transcription	Fetal Intestine Small	intestine
26	chr2:148736200-148752600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr2:148736200-148752800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr2:148736400-148744000	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr2:148736400-148747600	Weak transcription	Fetal Kidney	kidney
30	chr2:148736400-148750200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:148736400-148750400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr2:148736400-148750600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr2:148736400-148765600	Weak transcription	A549	lung
34	chr2:148736600-148744000	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr2:148736600-148752600	Weak transcription	Primary B cells from peripheral blood	blood
36	chr2:148736600-148752600	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr2:148737000-148753200	Weak transcription	Fetal Muscle Trunk	muscle
38	chr2:148737600-148747600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr2:148737600-148747800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr2:148737600-148752600	Weak transcription	Primary B cells from cord blood	blood
41	chr2:148737600-148752600	Weak transcription	Primary hematopoietic stem cells	blood
42	chr2:148739000-148750400	Weak transcription	Colon Smooth Muscle	Colon
43	chr2:148739000-148752600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr2:148739000-148759800	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr2:148741200-148747200	Weak transcription	Fetal Lung	lung
46	chr2:148741200-148758000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr2:148741600-148755800	Weak transcription	Ovary	ovary
48	chr2:148741600-148756200	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr2:148741800-148752800	Weak transcription	Thymus	Thymus
50	chr2:148741800-148757400	Weak transcription	Aorta	Aorta

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