Variant report

Variant	esv1793381
Chromosome Location	chr2:152370040-152463631
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:414)
CpG islands
(count:244)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr2:152384800-152384827	K562	blood:	n/a	n/a
3	BATF	chr2:152437230-152437561	GM12878	blood:	n/a	n/a
4	BATF	chr2:152458334-152458665	GM12878	blood:	n/a	n/a
5	BATF	chr2:152447781-152448112	GM12878	blood:	n/a	n/a
6	BCL11A	chr2:152447799-152448098	GM12878	blood:	n/a	n/a
7	BCL11A	chr2:152437248-152437547	GM12878	blood:	n/a	n/a
8	BCL11A	chr2:152458352-152458651	GM12878	blood:	n/a	n/a
9	BHLHE40	chr2:152384632-152384826	K562	blood:	n/a	n/a
10	CEBPB	chr2:152374039-152374079	K562	blood:	n/a	n/a
11	CEBPB	chr2:152453747-152454114	K562	blood:	n/a	n/a
12	CEBPB	chr2:152453798-152454061	K562	blood:	n/a	n/a
13	CEBPB	chr2:152374064-152374124	A549	lung:	n/a	n/a
14	CEBPB	chr2:152443242-152443477	K562	blood:	n/a	n/a
15	CEBPB	chr2:152391732-152391990	IMR90	lung:	n/a	chr2:152391865-152391876 chr2:152391866-152391877 chr2:152391867-152391876 chr2:152391865-152391878
16	CEBPB	chr2:152414468-152414617	K562	blood:	n/a	n/a
17	CEBPB	chr2:152373995-152374134	IMR90	lung:	n/a	n/a
18	CEBPB	chr2:152418839-152418984	HepG2	liver:	n/a	chr2:152418915-152418926
19	CEBPB	chr2:152443187-152443552	K562	blood:	n/a	n/a
20	CEBPB	chr2:152391737-152392008	HepG2	liver:	n/a	chr2:152391865-152391876 chr2:152391866-152391877 chr2:152391867-152391876 chr2:152391865-152391878
21	CEBPD	chr2:152448226-152448506	K562	blood:	n/a	n/a
22	CTCF	chr2:152419900-152420150	GM12875	blood:	n/a	n/a
23	CTCF	chr2:152437311-152437570	GM20000	blood:	n/a	n/a
24	CTCF	chr2:152458388-152458693	A549	lung:	n/a	n/a
25	CTCF	chr2:152458304-152458732	K562	blood:	n/a	n/a
26	CTCF	chr2:152458412-152458711	GM10248	blood:	n/a	n/a
27	CTCF	chr2:152453810-152454042	A549	lung:	n/a	n/a
28	CTCF	chr2:152383216-152383360	K562	blood:	n/a	n/a
29	CTCF	chr2:152383293-152383299	A549	lung:	n/a	n/a
30	CTCF	chr2:152447820-152448172	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr2:152437094-152437164	GM10248	blood:	n/a	n/a
32	CTCF	chr2:152437303-152437602	Lung_OC	lung:	n/a	n/a
33	CTCF	chr2:152447780-152448152	K562	blood:	n/a	n/a
34	CTCF	chr2:152447780-152447930	AG09309	skin:	n/a	n/a
35	CTCF	chr2:152437303-152437589	GM13977	blood:	n/a	n/a
36	CTCF	chr2:152448400-152448550	HMF	breast:	n/a	n/a
37	CTCF	chr2:152458415-152458693	GM13977	blood:	n/a	n/a
38	CTCF	chr2:152437284-152437589	A549	lung:	n/a	n/a
39	CTCF	chr2:152431980-152432130	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr2:152437270-152437607	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr2:152383256-152383295	GM19240	blood:	n/a	n/a
42	CTCF	chr2:152448240-152448390	AG10803	skin:	n/a	n/a
43	CTCF	chr2:152458373-152458722	K562	blood:	n/a	n/a
44	CTCF	chr2:152436283-152436344	Lung_OC	lung:	n/a	n/a
45	CTCF	chr2:152458274-152458761	A549	lung:	n/a	n/a
46	CTCF	chr2:152448265-152448298	GM13977	blood:	n/a	n/a
47	CTCF	chr2:152447841-152448151	GM10248	blood:	n/a	n/a
48	CTCF	chr2:152438351-152438392	GM10266	blood:	n/a	n/a
49	CTCF	chr2:152447858-152447944	A549	lung:	n/a	n/a
50	CTCF	chr2:152443192-152443631	A549	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:152402878-152402928	Caco-2	colon:	n/a
2	chr2:152385032-152385082	ovcar-3	ovarian:	n/a
3	chr2:152440445-152440495	Jurkat	blood:	n/a
4	chr2:152385032-152385082	NT2-D1	testis:	n/a
5	chr2:152402878-152402928	HIPEpiC	eye:	n/a
6	chr2:152402878-152402928	SK-N-SH_RA	brain:	n/a
7	chr2:152378577-152378627	T-47D	breast:	n/a
8	chr2:152402878-152402928	ECC-1	luminal epithelium:	n/a
9	chr2:152402878-152402928	BE2_C	brain:	n/a
10	chr2:152402878-152402928	IMR90	lung:	fetal
11	chr2:152378577-152378627	SK-N-SH_RA	brain:	n/a
12	chr2:152378577-152378627	PANC-1	pancreas:	n/a
13	chr2:152402878-152402928	AG04449	skin:	fetal
14	chr2:152440445-152440495	RPTEC	kidney:	n/a
15	chr2:152378577-152378627	PrEC	prostate:	n/a
16	chr2:152385032-152385082	HAEpiC	amniotic membrane:	n/a
17	chr2:152378577-152378627	HEEpiC	esophagus:	n/a
18	chr2:152440445-152440495	A549	lung:	n/a
19	chr2:152378577-152378627	AG04449	skin:	fetal
20	chr2:152385032-152385082	GM12891	blood:	n/a
21	chr2:152385032-152385082	SK-N-SH_RA	brain:	n/a
22	chr2:152402878-152402928	PFSK-1	brain:	n/a
23	chr2:152378577-152378627	GM12891	blood:	n/a
24	chr2:152385032-152385082	HRPEpiC	eye:	n/a
25	chr2:152378577-152378627	Jurkat	blood:	n/a
26	chr2:152402878-152402928	HepG2	liver:	n/a
27	chr2:152378577-152378627	U87	brain:	n/a
28	chr2:152378577-152378627	LNCaP	prostate:	n/a
29	chr2:152378577-152378627	A549	lung:	n/a
30	chr2:152385032-152385082	LNCaP	prostate:	n/a
31	chr2:152402878-152402928	Hela-S3	cervix:	n/a
32	chr2:152402878-152402928	T-47D	breast:	n/a
33	chr2:152385032-152385082	AG04450	lung:	fetal
34	chr2:152440445-152440495	HEK293	kidney:	embryo
35	chr2:152440445-152440495	CMK	blood:	n/a
36	chr2:152378577-152378627	AG04450	lung:	fetal
37	chr2:152402878-152402928	H1-hESC	embryonic stem cell:	embryo
38	chr2:152402878-152402928	HEK293	kidney:	embryo
39	chr2:152440445-152440495	HRE	kidney:	n/a
40	chr2:152385032-152385082	BJ	skin:	n/a
41	chr2:152440445-152440495	HepG2	liver:	n/a
42	chr2:152385032-152385082	A549	lung:	n/a
43	chr2:152402878-152402928	AG04450	lung:	fetal
44	chr2:152378577-152378627	CMK	blood:	n/a
45	chr2:152378577-152378627	HepG2	liver:	n/a
46	chr2:152402878-152402928	SKMC	muscle:	n/a
47	chr2:152402878-152402928	PANC-1	pancreas:	n/a
48	chr2:152440445-152440495	AoSMC	blood vessel:	n/a
49	chr2:152440445-152440495	GM12891	blood:	n/a
50	chr2:152440445-152440495	NH-A	brain:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:152398754..152402722-chr2:152404309..152407409,3	K562	blood:
2	chr2:152398924..152401108-chr2:152404034..152405550,2	K562	blood:
3	chr2:152360419..152362354-chr2:152373826..152376342,2	K562	blood:
4	chr2:152420725..152422914-chr2:152422923..152425843,3	MCF-7	breast:
5	chr2:152402480..152405227-chr2:152409026..152411315,2	K562	blood:
6	chr2:152398754..152402722-chr2:152404309..152407409,3	K562	blood:
7	chr1:149813957..149815657-chr2:152394673..152396322,2	MCF-7	breast:
8	chr2:152366454..152368368-chr2:152374730..152376370,2	MCF-7	breast:
9	chr2:152414320..152417036-chr2:152422973..152425873,2	K562	blood:
10	chr2:152414320..152417036-chr2:152422973..152425873,2	K562	blood:
11	chr2:152423732..152425326-chr2:152425773..152428506,2	K562	blood:
12	chr2:152396825..152398789-chr2:152409057..152411603,2	K562	blood:
13	chr2:152398924..152401108-chr2:152404034..152405550,2	K562	blood:
14	chr2:152420294..152421848-chr2:152423349..152426128,2	K562	blood:
15	chr2:152394167..152396602-chr2:152404193..152405928,2	K562	blood:
16	chr2:152392031..152396031-chr2:152396144..152400510,4	K562	blood:
17	chr2:152382125..152384924-chr2:152385395..152388332,2	K562	blood:
18	chr2:152392901..152394420-chr2:152407078..152409911,2	K562	blood:
19	chr2:152402480..152405227-chr2:152409026..152411315,2	K562	blood:
20	chr2:152394531..152397310-chr2:152397925..152400896,2	K562	blood:
21	chr2:152423732..152425326-chr2:152425773..152428506,2	K562	blood:
22	chr2:152420294..152421848-chr2:152423349..152426128,2	K562	blood:
23	chr2:152389412..152391698-chr2:152393142..152395709,2	MCF-7	breast:
24	chr2:152389412..152391698-chr2:152393142..152395709,2	MCF-7	breast:
25	chr2:152392901..152394420-chr2:152407078..152409911,2	K562	blood:
26	chr2:152420725..152422914-chr2:152422923..152425843,3	MCF-7	breast:
27	chr2:152394167..152396602-chr2:152404193..152405928,2	K562	blood:

No data

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

Extended variants
information (count: 2755 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:2755 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117694074	chr2:152370051-152370052	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs16830128	chr2:152370052-152370053	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs375216341	chr2:152370070-152370071	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75221580	chr2:152370078-152370079	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551898907	chr2:152370087-152370088	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs112057574	chr2:152370093-152370094	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571808208	chr2:152370120-152370121	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs372387518	chr2:152370137-152370138	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs376977065	chr2:152370189-152370190	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs200963111	chr2:152370194-152370195	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs569849433	chr2:152370201-152370202	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs561926406	chr2:152370210-152370211	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs369229042	chr2:152370225-152370226	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs535373507	chr2:152370232-152370233	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs142042367	chr2:152370262-152370263	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs565333645	chr2:152370280-152370281	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs534356975	chr2:152370295-152370296	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs556560430	chr2:152370318-152370319	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs573437684	chr2:152370321-152370322	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs370002963	chr2:152370351-152370352	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs145900263	chr2:152370382-152370383	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs16830130	chr2:152370399-152370400	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs374950634	chr2:152370404-152370405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543524715	chr2:152370469-152370470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557237512	chr2:152370481-152370482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147769181	chr2:152370489-152370490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542928634	chr2:152370521-152370522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369051192	chr2:152370555-152370556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373854612	chr2:152370621-152370622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560132337	chr2:152370665-152370666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs180861698	chr2:152370676-152370677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372680599	chr2:152370795-152370796	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs141178569	chr2:152370806-152370807	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs200113036	chr2:152370809-152370810	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs112610938	chr2:152370830-152370831	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs112450383	chr2:152370831-152370832	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs373105485	chr2:152370861-152370862	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs369098763	chr2:152370899-152370900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563896790	chr2:152370904-152370905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372699411	chr2:152370908-152370909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374941096	chr2:152370911-152370912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111314898	chr2:152370945-152370946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150471104	chr2:152370963-152370964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569729941	chr2:152371001-152371002	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs529135164	chr2:152371026-152371027	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs138333783	chr2:152371062-152371063	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs565598716	chr2:152371129-152371130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534606943	chr2:152371153-152371154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76123095	chr2:152371228-152371229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570924936	chr2:152371276-152371277	Weak transcription Strong 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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:266 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152267600-152379400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:152324200-152382400	Weak transcription	Aorta	Aorta
3	chr2:152340400-152371000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr2:152341600-152390600	Weak transcription	Left Ventricle	heart
5	chr2:152343200-152422200	Weak transcription	Primary B cells from cord blood	blood
6	chr2:152343400-152371000	Weak transcription	Adipose Nuclei	Adipose
7	chr2:152343400-152373000	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr2:152347000-152387200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr2:152348800-152400800	Strong transcription	Skeletal Muscle Female	skeletal muscle
10	chr2:152358600-152394000	Weak transcription	Spleen	Spleen
11	chr2:152359400-152382200	Weak transcription	Primary B cells from peripheral blood	blood
12	chr2:152359800-152376400	Strong transcription	Fetal Muscle Trunk	muscle
13	chr2:152360400-152376000	Strong transcription	Fetal Muscle Leg	muscle
14	chr2:152360800-152424400	Weak transcription	Brain Anterior Caudate	brain
15	chr2:152361000-152387800	Strong transcription	HSMMtube	muscle
16	chr2:152363200-152391800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr2:152364600-152377600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr2:152365200-152385200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr2:152365200-152415600	Weak transcription	Fetal Intestine Small	intestine
20	chr2:152365400-152377000	Weak transcription	Placenta	Placenta
21	chr2:152365400-152377600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr2:152367400-152370400	Strong transcription	Psoas Muscle	Psoas
23	chr2:152370000-152370400	Genic enhancers	Skeletal Muscle Male	skeletal muscle
24	chr2:152370400-152373800	Weak transcription	Psoas Muscle	Psoas
25	chr2:152370400-152403600	Strong transcription	Skeletal Muscle Male	skeletal muscle
26	chr2:152371400-152421000	Weak transcription	Pancreas	Pancrea
27	chr2:152373800-152374200	Strong transcription	Psoas Muscle	Psoas
28	chr2:152374200-152385600	Weak transcription	Psoas Muscle	Psoas
29	chr2:152375400-152377600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr2:152376000-152377400	Weak transcription	Fetal Muscle Leg	muscle
31	chr2:152376400-152380200	Weak transcription	Fetal Muscle Trunk	muscle
32	chr2:152377000-152378000	Enhancers	Placenta	Placenta
33	chr2:152377200-152377800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr2:152377200-152391800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr2:152377400-152378000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:152377400-152378400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:152377400-152378400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr2:152377400-152378600	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr2:152377400-152393800	Strong transcription	Fetal Muscle Leg	muscle
40	chr2:152377600-152377800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr2:152377600-152378000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr2:152377600-152378000	Enhancers	H9 Cell Line	embryonic stem cell
43	chr2:152377600-152378000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr2:152377600-152378200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr2:152377600-152378200	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr2:152377600-152378200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr2:152377600-152378200	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr2:152377600-152378400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr2:152377600-152378400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr2:152377600-152378400	Enhancers	HUES6 Cell Line	embryonic stem cell

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