Variant report

Variant	esv3693428
Chromosome Location	chr2:152320932-152434896
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:476)
CpG islands
(count:366)
Chromatin interactive
region (count:57)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:476 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:152416770-152417027	K562	blood:	n/a	n/a
2	BACH1	chr2:152321150-152322834	K562	blood:	n/a	n/a
3	BACH1	chr2:152384800-152384827	K562	blood:	n/a	n/a
4	BACH1	chr2:152329594-152329776	K562	blood:	n/a	n/a
5	BATF	chr2:152338185-152338626	GM12878	blood:	n/a	n/a
6	BATF	chr2:152338242-152338516	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:152384632-152384826	K562	blood:	n/a	n/a
8	CEBPB	chr2:152374064-152374124	A549	lung:	n/a	n/a
9	CEBPB	chr2:152418839-152418984	HepG2	liver:	n/a	chr2:152418915-152418926
10	CEBPB	chr2:152332558-152332671	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:152391732-152391990	IMR90	lung:	n/a	chr2:152391865-152391876 chr2:152391866-152391877 chr2:152391867-152391876 chr2:152391865-152391878
12	CEBPB	chr2:152338148-152338364	IMR90	lung:	n/a	chr2:152338230-152338239 chr2:152338228-152338239
13	CEBPB	chr2:152373995-152374134	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:152374039-152374079	K562	blood:	n/a	n/a
15	CEBPB	chr2:152332582-152332598	A549	lung:	n/a	n/a
16	CEBPB	chr2:152334787-152334886	K562	blood:	n/a	n/a
17	CEBPB	chr2:152414468-152414617	K562	blood:	n/a	n/a
18	CEBPB	chr2:152338063-152338359	HepG2	liver:	n/a	chr2:152338230-152338239 chr2:152338228-152338239
19	CEBPB	chr2:152391737-152392008	HepG2	liver:	n/a	chr2:152391865-152391876 chr2:152391866-152391877 chr2:152391867-152391876 chr2:152391865-152391878
20	CTCF	chr2:152432000-152432150	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr2:152337400-152337550	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr2:152383303-152383325	K562	blood:	n/a	n/a
23	CTCF	chr2:152432080-152432230	HMF	breast:	n/a	n/a
24	CTCF	chr2:152383265-152383299	MCF-7	breast:	n/a	n/a
25	CTCF	chr2:152322683-152322710	K562	blood:	n/a	n/a
26	CTCF	chr2:152431960-152432110	HMF	breast:	n/a	n/a
27	CTCF	chr2:152383174-152383421	K562	blood:	n/a	n/a
28	CTCF	chr2:152383256-152383295	GM19240	blood:	n/a	n/a
29	CTCF	chr2:152429101-152429145	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr2:152383180-152383330	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr2:152397000-152397150	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr2:152383237-152383326	GM12892	blood:	n/a	n/a
33	CTCF	chr2:152342340-152342490	NB4	blood:	n/a	n/a
34	CTCF	chr2:152383337-152383339	GM19239	blood:	n/a	n/a
35	CTCF	chr2:152334461-152334519	GM10266	blood:	n/a	n/a
36	CTCF	chr2:152383219-152383337	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:152432058-152432090	A549	lung:	n/a	n/a
38	CTCF	chr2:152383060-152383210	GM06990	blood:	n/a	n/a
39	CTCF	chr2:152383293-152383299	A549	lung:	n/a	n/a
40	CTCF	chr2:152383216-152383360	K562	blood:	n/a	n/a
41	CTCF	chr2:152383171-152383380	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr2:152384797-152384827	K562	blood:	n/a	n/a
43	CTCF	chr2:152383214-152383363	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr2:152383230-152383316	GM12891	blood:	n/a	n/a
45	CTCF	chr2:152383200-152383350	A549	lung:	n/a	n/a
46	CTCF	chr2:152383217-152383336	GM19239	blood:	n/a	n/a
47	CTCF	chr2:152383214-152383352	GM19238	blood:	n/a	n/a
48	CTCF	chr2:152431980-152432130	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr2:152396760-152396910	HAc	cerebellar:	n/a	n/a
50	CTCF	chr2:152383200-152383350	GM12871	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:152378577-152378627	HL-60	blood:	n/a
2	chr2:152331806-152331856	HEEpiC	esophagus:	n/a
3	chr2:152378577-152378627	NHBE	bronchial:	n/a
4	chr2:152385032-152385082	IMR90	lung:	fetal
5	chr2:152349105-152349155	H1-hESC	embryonic stem cell:	embryo
6	chr2:152342216-152342266	SAEC	small airway:	n/a
7	chr2:152378577-152378627	ECC-1	luminal epithelium:	n/a
8	chr2:152385032-152385082	AG09319	gingival:	n/a
9	chr2:152331806-152331856	HepG2	liver:	n/a
10	chr2:152402878-152402928	Caco-2	colon:	n/a
11	chr2:152349105-152349155	GM12878	blood:	n/a
12	chr2:152331806-152331856	CMK	blood:	n/a
13	chr2:152342216-152342266	SK-N-SH_RA	brain:	n/a
14	chr2:152349105-152349155	MCF-7	breast:	n/a
15	chr2:152385032-152385082	H1-hESC	embryonic stem cell:	embryo
16	chr2:152378577-152378627	HNPCEpiC	eye:	n/a
17	chr2:152378577-152378627	HCT-116	colon:	n/a
18	chr2:152342216-152342266	ECC-1	luminal epithelium:	n/a
19	chr2:152331806-152331856	IMR90	lung:	fetal
20	chr2:152385032-152385082	PFSK-1	brain:	n/a
21	chr2:152378577-152378627	IMR90	lung:	fetal
22	chr2:152402878-152402928	GM19239	blood:	n/a
23	chr2:152349105-152349155	SK-N-SH	brain:	n/a
24	chr2:152378577-152378627	PFSK-1	brain:	n/a
25	chr2:152331806-152331856	ProgFib	skin:	n/a
26	chr2:152378577-152378627	GM06990	blood:	n/a
27	chr2:152331806-152331856	GM12891	blood:	n/a
28	chr2:152331806-152331856	HRE	kidney:	n/a
29	chr2:152331806-152331856	HCM	heart:	n/a
30	chr2:152331806-152331856	ovcar-3	ovarian:	n/a
31	chr2:152378577-152378627	SK-N-MC	brain:	n/a
32	chr2:152349105-152349155	HIPEpiC	eye:	n/a
33	chr2:152378577-152378627	AG04450	lung:	fetal
34	chr2:152342216-152342266	HPAEpiC	pulmonary alveolar:	n/a
35	chr2:152342216-152342266	PFSK-1	brain:	n/a
36	chr2:152385032-152385082	NB4	blood:	n/a
37	chr2:152342216-152342266	NT2-D1	testis:	n/a
38	chr2:152385032-152385082	AG10803	skin:	n/a
39	chr2:152331806-152331856	Hela-S3	cervix:	n/a
40	chr2:152331806-152331856	MCF10A-Er-Src	breast:	n/a
41	chr2:152402878-152402928	NHBE	bronchial:	n/a
42	chr2:152342216-152342266	Jurkat	blood:	n/a
43	chr2:152349105-152349155	LNCaP	prostate:	n/a
44	chr2:152378577-152378627	Caco-2	colon:	n/a
45	chr2:152342216-152342266	HEK293	kidney:	embryo
46	chr2:152402878-152402928	HMEC	breast:	n/a
47	chr2:152378577-152378627	MCF-7	breast:	n/a
48	chr2:152342216-152342266	H1-hESC	embryonic stem cell:	embryo
49	chr2:152331806-152331856	HRPEpiC	eye:	n/a
50	chr2:152385032-152385082	HRE	kidney:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:152345538..152348326-chr2:152350633..152352626,2	MCF-7	breast:
2	chr2:152347893..152350567-chr2:152361417..152364168,2	K562	blood:
3	chr2:152398924..152401108-chr2:152404034..152405550,2	K562	blood:
4	chr2:152392901..152394420-chr2:152407078..152409911,2	K562	blood:
5	chr2:152351759..152353707-chr2:152360537..152362140,2	K562	blood:
6	chr2:152319808..152322653-chr2:152331004..152333072,2	K562	blood:
7	chr2:152420294..152421848-chr2:152423349..152426128,2	K562	blood:
8	chr2:152366454..152368368-chr2:152374730..152376370,2	MCF-7	breast:
9	chr2:152394531..152397310-chr2:152397925..152400896,2	K562	blood:
10	chr2:152329723..152332173-chr2:152332317..152334542,2	K562	blood:
11	chr2:152420294..152421848-chr2:152423349..152426128,2	K562	blood:
12	chr1:149813957..149815657-chr2:152394673..152396322,2	MCF-7	breast:
13	chr2:152389412..152391698-chr2:152393142..152395709,2	MCF-7	breast:
14	chr2:152333499..152335226-chr2:152337769..152339551,2	K562	blood:
15	chr2:152117786..152119575-chr2:152331132..152333379,2	MCF-7	breast:
16	chr2:152322769..152325475-chr2:152328124..152330631,2	K562	blood:
17	chr2:152402480..152405227-chr2:152409026..152411315,2	K562	blood:
18	chr2:152398924..152401108-chr2:152404034..152405550,2	K562	blood:
19	chr2:152394167..152396602-chr2:152404193..152405928,2	K562	blood:
20	chr2:152336512..152339181-chr2:152360323..152362422,2	K562	blood:
21	chr2:152360419..152362354-chr2:152373826..152376342,2	K562	blood:
22	chr2:152398754..152402722-chr2:152404309..152407409,3	K562	blood:
23	chr2:152394167..152396602-chr2:152404193..152405928,2	K562	blood:
24	chr2:152351759..152353707-chr2:152360537..152362140,2	K562	blood:
25	chr2:152344851..152347246-chr2:152350528..152353460,3	K562	blood:
26	chr2:152320561..152322132-chr2:152322755..152325305,2	MCF-7	breast:
27	chr2:152336512..152339181-chr2:152360323..152362422,2	K562	blood:
28	chr2:152329635..152332984-chr2:152337072..152339089,3	K562	blood:
29	chr2:152414320..152417036-chr2:152422973..152425873,2	K562	blood:
30	chr2:152364952..152367436-chr2:152369913..152371576,2	K562	blood:
31	chr2:152333499..152335226-chr2:152337769..152339551,2	K562	blood:
32	chr2:152398754..152402722-chr2:152404309..152407409,3	K562	blood:
33	chr2:152322769..152325475-chr2:152328124..152330631,2	K562	blood:
34	chr2:152392901..152394420-chr2:152407078..152409911,2	K562	blood:
35	chr2:152333590..152335850-chr2:152341846..152344009,2	K562	blood:
36	chr2:152360209..152362131-chr2:152365151..152367000,2	K562	blood:
37	chr2:152414320..152417036-chr2:152422973..152425873,2	K562	blood:
38	chr2:152360209..152362131-chr2:152365151..152367000,2	K562	blood:
39	chr2:152423732..152425326-chr2:152425773..152428506,2	K562	blood:
40	chr2:152329723..152332173-chr2:152332317..152334542,2	K562	blood:
41	chr2:152355139..152355815-chr2:152882008..152882831,2	K562	blood:
42	chr2:152420725..152422914-chr2:152422923..152425843,3	MCF-7	breast:
43	chr2:152362583..152365048-chr2:152368059..152369746,2	K562	blood:
44	chr2:152420725..152422914-chr2:152422923..152425843,3	MCF-7	breast:
45	chr2:152107619..152109429-chr2:152322968..152325434,2	K562	blood:
46	chr2:152392031..152396031-chr2:152396144..152400510,4	K562	blood:
47	chr2:152382125..152384924-chr2:152385395..152388332,2	K562	blood:
48	chr2:152423732..152425326-chr2:152425773..152428506,2	K562	blood:
49	chr2:152360419..152362354-chr2:152373826..152376342,2	K562	blood:
50	chr2:152343156..152345753-chr2:152361266..152362840,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNFAIP6-7	chr2:152364243-152364274	NONHSAT074960
2	lnc-TNFAIP6-6	chr2:152342791-152343270	NONHSAT074958
3	lnc-TNFAIP6-6	chr2:152354300-152354727	NONHSAT074958
4	lnc-NMI-6	chr2:152365077-152365387	expReg_chr2_10875_-
5	lnc-TNFAIP6-5	chr2:152332640-152333850	NONHSAT074957
6	lnc-TNFAIP6-6	chr2:152351489-152351840	NONHSAT074959
7	lnc-NMI-4	chr2:152362670-152363001	expReg_chr2_10865_-
8	lnc-NMI-3	chr2:152361579-152361850	expReg_chr2_10858_-
9	lnc-TNFAIP6-6	chr2:152354300-152354729	NONHSAT074959
10	lnc-TNFAIP6-7	chr2:152362462-152362889	NONHSAT074961
11	lnc-TNFAIP6-7	chr2:152362316-152362889	NONHSAT074960
12	lnc-NMI-5	chr2:152363586-152363988	expReg_chr2_10870_-
13	lnc-TNFAIP6-7	chr2:152363510-152363626	NONHSAT074961
14	lnc-TNFAIP6-6	chr2:152351743-152351840	NONHSAT074958

No data

Variant related genes	Relation type
RIF1	TF binding region
NEB	TF binding region
RIF1	CpG island
NEB	CpG island
ENSG00000184898	chromatin interactions
ENSG00000183091	chromatin interactions
ENSG00000183558	chromatin interactions
ENSG00000220323	chromatin interactions
ENSG00000080345	chromatin interactions

Extended variants
information (count: 4528 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:4528 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13390456	chr2:152320932-152320933	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs373435312	chr2:152320962-152320963	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs199663670	chr2:152320976-152320977	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs371158008	chr2:152321011-152321012	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs61748232	chr2:152321027-152321028	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs375421586	chr2:152321035-152321036	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs367837370	chr2:152321044-152321045	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs371731867	chr2:152321045-152321046	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs374121051	chr2:152321067-152321068	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs367993129	chr2:152321080-152321081	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs3732305	chr2:152321090-152321091	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs61748233	chr2:152321091-152321092	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs143956653	chr2:152321110-152321111	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs535432987	chr2:152321149-152321150	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs201978998	chr2:152321155-152321156	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs201874472	chr2:152321163-152321164	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs370699631	chr2:152321177-152321178	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs147739440	chr2:152321204-152321205	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs201122966	chr2:152321246-152321247	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150672982	chr2:152321272-152321273	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553538022	chr2:152321302-152321303	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200726516	chr2:152321303-152321304	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200607345	chr2:152321325-152321326	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75052096	chr2:152321331-152321332	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369431913	chr2:152321333-152321334	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148837520	chr2:152321342-152321343	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200365768	chr2:152321353-152321354	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200887608	chr2:152321377-152321378	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372412176	chr2:152321392-152321393	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376681380	chr2:152321429-152321430	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201753159	chr2:152321440-152321441	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs199656210	chr2:152321447-152321448	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113274748	chr2:152321451-152321452	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188032134	chr2:152321457-152321458	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369136350	chr2:152321498-152321499	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs61748234	chr2:152321516-152321517	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200831918	chr2:152321538-152321539	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373597774	chr2:152321539-152321540	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs202043885	chr2:152321544-152321545	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572149191	chr2:152321552-152321553	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559164678	chr2:152321595-152321596	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377658734	chr2:152321596-152321597	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2444258	chr2:152321618-152321619	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs371114356	chr2:152321622-152321623	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374686638	chr2:152321625-152321626	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536244464	chr2:152321642-152321643	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138726655	chr2:152321662-152321663	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140008446	chr2:152321664-152321665	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147309560	chr2:152321679-152321680	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550349739	chr2:152321687-152321688	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

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
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
Hodgkin''s lymphoma	18179710	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19156171	CNVD
Acute myeloid leukemia	18000384	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1077 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152267600-152379400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:152267800-152340400	Weak transcription	Stomach Mucosa	stomach
3	chr2:152268000-152342800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr2:152268200-152327800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr2:152268200-152328400	Strong transcription	H1 Cell Line	embryonic stem cell
6	chr2:152268200-152328600	Strong transcription	Fetal Thymus	thymus
7	chr2:152268400-152327800	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr2:152268600-152326800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr2:152268600-152327800	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr2:152268600-152334400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr2:152268600-152342600	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr2:152268800-152326800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr2:152268800-152327800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr2:152268800-152327800	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr2:152269400-152327200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr2:152272400-152327800	Strong transcription	Dnd41	blood
17	chr2:152283800-152334000	Strong transcription	Primary T cells fromperipheralblood	blood
18	chr2:152284200-152327000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr2:152284600-152327800	Strong transcription	HepG2	liver
20	chr2:152285000-152327800	Strong transcription	Placenta	Placenta
21	chr2:152285200-152327600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr2:152285200-152327800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr2:152285200-152331200	Strong transcription	Adipose Nuclei	Adipose
24	chr2:152290600-152323400	Weak transcription	Aorta	Aorta
25	chr2:152291800-152321000	Strong transcription	Duodenum Mucosa	Duodenum
26	chr2:152294400-152321400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr2:152294600-152327800	Strong transcription	Primary T helper cells PMA-I stimulated	--
28	chr2:152294800-152327800	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr2:152295800-152348400	Weak transcription	Right Ventricle	heart
30	chr2:152298600-152327600	Strong transcription	HUVEC	blood vessel
31	chr2:152300000-152333400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr2:152300200-152327800	Strong transcription	K562	blood
33	chr2:152301600-152324400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr2:152301800-152343800	Weak transcription	Gastric	stomach
35	chr2:152303200-152325000	Weak transcription	Small Intestine	intestine
36	chr2:152303400-152326400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:152304800-152322800	Strong transcription	Osteobl	bone
38	chr2:152304800-152354000	Weak transcription	Spleen	Spleen
39	chr2:152306200-152322800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr2:152306400-152324800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr2:152306800-152328400	Strong transcription	Fetal Muscle Trunk	muscle
42	chr2:152307000-152328000	Strong transcription	Rectal Mucosa Donor 31	rectum
43	chr2:152307600-152327600	Strong transcription	Primary B cells from cord blood	blood
44	chr2:152307600-152327800	Strong transcription	HSMM	muscle
45	chr2:152307600-152328000	Strong transcription	Liver	Liver
46	chr2:152308000-152322000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr2:152309000-152327800	Strong transcription	Fetal Intestine Large	intestine
48	chr2:152310200-152321000	Strong transcription	Muscle Satellite Cultured Cells	--
49	chr2:152311400-152321000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr2:152311800-152323600	Strong transcription	Fetal Kidney	kidney

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