Variant report

Variant	nsv1013164
Chromosome Location	chr2:212352672-212416215
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:189)
CpG islands
(count:184)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:189 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:212363692-212363815	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr2:212375518-212375530	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr2:212363575-212363885	H1-hESC	embryonic stem cell:	n/a	chr2:212363681-212363692
4	CEBPB	chr2:212355456-212355746	HepG2	liver:	n/a	chr2:212355578-212355589 chr2:212355580-212355591
5	CEBPB	chr2:212414722-212414939	HepG2	liver:	n/a	chr2:212414816-212414827
6	CEBPB	chr2:212363646-212363764	HepG2	liver:	n/a	chr2:212363681-212363692
7	CEBPB	chr2:212357657-212358022	IMR90	lung:	n/a	n/a
8	CEBPB	chr2:212377956-212378135	HepG2	liver:	n/a	chr2:212378026-212378037
9	CEBPB	chr2:212357683-212357979	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr2:212357678-212358005	A549	lung:	n/a	n/a
11	CEBPB	chr2:212372106-212372296	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr2:212357692-212358007	HepG2	liver:	n/a	n/a
13	CHD2	chr2:212363638-212363823	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr2:212368680-212368830	HEK293	kidney:	n/a	n/a
15	CTCF	chr2:212368640-212368790	HMEC	breast:	n/a	n/a
16	CTCF	chr2:212367940-212368090	GM12873	blood:	n/a	n/a
17	CTCF	chr2:212368680-212368830	RPTEC	kidney:	n/a	n/a
18	CTCF	chr2:212368707-212368833	GM10266	blood:	n/a	n/a
19	CTCF	chr2:212406424-212406426	GM12878	blood:	n/a	n/a
20	CTCF	chr2:212368669-212368870	GM12891	blood:	n/a	n/a
21	CTCF	chr2:212368720-212368870	MCF-7	breast:	n/a	n/a
22	CTCF	chr2:212368678-212368869	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr2:212368660-212368810	HVMF	connective:	n/a	n/a
24	CTCF	chr2:212368620-212368770	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr2:212368713-212368825	GM20000	blood:	n/a	n/a
26	CTCF	chr2:212368660-212368810	GM12868	blood:	n/a	n/a
27	CTCF	chr2:212368700-212368850	HAc	cerebellar:	n/a	n/a
28	CTCF	chr2:212368740-212368890	GM12870	blood:	n/a	n/a
29	CTCF	chr2:212368683-212368861	MCF-7	breast:	n/a	n/a
30	CTCF	chr2:212368621-212368821	K562	blood:	n/a	n/a
31	CTCF	chr2:212368700-212368850	A549	lung:	n/a	n/a
32	CTCF	chr2:212368640-212368790	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr2:212368680-212368830	HMF	breast:	n/a	n/a
34	CTCF	chr2:212368620-212368770	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr2:212368740-212368890	GM12865	blood:	n/a	n/a
36	CTCF	chr2:212368520-212368670	RPTEC	kidney:	n/a	n/a
37	CTCF	chr2:212368720-212368870	GM06990	blood:	n/a	n/a
38	CTCF	chr2:212389640-212389790	BE2_C	brain:	n/a	n/a
39	CTCF	chr2:212368700-212368850	Caco-2	colon:	n/a	n/a
40	CTCF	chr2:212354920-212355070	BE2_C	brain:	n/a	n/a
41	CTCF	chr2:212368700-212368850	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr2:212368640-212368790	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr2:212368644-212368847	GM13977	blood:	n/a	n/a
44	CTCF	chr2:212368687-212368856	K562	blood:	n/a	n/a
45	CTCF	chr2:212368740-212368890	HRE	kidney:	n/a	n/a
46	CTCF	chr2:212368680-212368830	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr2:212368720-212368870	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr2:212368694-212368835	LNCaP	prostate:	n/a	n/a
49	CTCF	chr2:212368640-212368790	K562	blood:	n/a	n/a
50	CTCF	chr2:212368750-212368829	HUVEC	blood vessel:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:212389424-212389474	SK-N-MC	brain:	n/a
2	chr2:212389424-212389474	SK-N-MC	brain:	n/a
3	chr2:212363715-212363765	SK-N-MC	brain:	n/a
4	chr2:212389424-212389474	HCF	heart:	n/a
5	chr2:212389424-212389474	NHDF-neo	bronchial:	n/a
6	chr2:212389424-212389474	RPTEC	kidney:	n/a
7	chr2:212389424-212389474	HRCEpiC	kidney:	n/a
8	chr2:212389424-212389474	HCM	heart:	n/a
9	chr2:212363715-212363765	AG09309	skin:	n/a
10	chr2:212389424-212389474	AG04449	skin:	fetal
11	chr2:212363715-212363765	U87	brain:	n/a
12	chr2:212389424-212389474	GM12878	blood:	n/a
13	chr2:212363715-212363765	SAEC	small airway:	n/a
14	chr2:212363715-212363765	NHDF-neo	bronchial:	n/a
15	chr2:212389424-212389474	LNCaP	prostate:	n/a
16	chr2:212363715-212363765	HUVEC	blood vessel:	n/a
17	chr2:212389424-212389474	NT2-D1	testis:	n/a
18	chr2:212389424-212389474	H1-hESC	embryonic stem cell:	embryo
19	chr2:212363715-212363765	HCT-116	colon:	n/a
20	chr2:212363715-212363765	NB4	blood:	n/a
21	chr2:212363715-212363765	HL-60	blood:	n/a
22	chr2:212389424-212389474	ovcar-3	ovarian:	n/a
23	chr2:212389424-212389474	HEEpiC	esophagus:	n/a
24	chr2:212389424-212389474	AG04450	lung:	fetal
25	chr2:212363715-212363765	Caco-2	colon:	n/a
26	chr2:212388373-212388423	NHDF-neo	bronchial:	n/a
27	chr2:212363715-212363765	HRE	kidney:	n/a
28	chr2:212388373-212388423	HEEpiC	esophagus:	n/a
29	chr2:212388373-212388423	A549	lung:	n/a
30	chr2:212363715-212363765	GM12878	blood:	n/a
31	chr2:212389424-212389474	CMK	blood:	n/a
32	chr2:212388373-212388423	HAEpiC	amniotic membrane:	n/a
33	chr2:212388373-212388423	CMK	blood:	n/a
34	chr2:212389424-212389474	NH-A	brain:	n/a
35	chr2:212363715-212363765	Hepatocyte	liver:	n/a
36	chr2:212388373-212388423	ECC-1	luminal epithelium:	n/a
37	chr2:212388373-212388423	BJ	skin:	n/a
38	chr2:212388373-212388423	Jurkat	blood:	n/a
39	chr2:212363715-212363765	NH-A	brain:	n/a
40	chr2:212363715-212363765	SK-N-SH	brain:	n/a
41	chr2:212389424-212389474	MCF10A-Er-Src	breast:	n/a
42	chr2:212388373-212388423	HPAEpiC	pulmonary alveolar:	n/a
43	chr2:212388373-212388423	AG10803	skin:	n/a
44	chr2:212388373-212388423	IMR90	lung:	fetal
45	chr2:212388373-212388423	Hepatocyte	liver:	n/a
46	chr2:212389424-212389474	HNPCEpiC	eye:	n/a
47	chr2:212389424-212389474	NHBE	bronchial:	n/a
48	chr2:212389424-212389474	ECC-1	luminal epithelium:	n/a
49	chr2:212363715-212363765	PFSK-1	brain:	n/a
50	chr2:212388373-212388423	HIPEpiC	eye:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:203274022..203274758-chr2:212363047..212363985,2	MCF-7	breast:
2	chr2:212366946..212368723-chr2:212370212..212371913,2	K562	blood:
3	chr2:212320246..212322831-chr2:212376794..212379145,2	MCF-7	breast:
4	chr2:212352611..212354767-chr2:212356529..212358511,2	MCF-7	breast:
5	chr2:212349648..212351176-chr2:212354643..212357480,2	MCF-7	breast:
6	chr2:212408584..212410240-chr2:212416395..212418822,2	MCF-7	breast:
7	chr2:212366946..212368723-chr2:212370212..212371913,2	K562	blood:
8	chr2:212352611..212354767-chr2:212356529..212358511,2	MCF-7	breast:
9	chr2:212288710..212290756-chr2:212380740..212383126,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNA5SP119	TF binding region
RNA5SP119	CpG island
ENSG00000233791	chromatin interactions
ENSG00000159388	chromatin interactions

Extended variants
information (count: 2743 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2743 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565531375	chr2:212352711-212352712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534659865	chr2:212352737-212352738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183995216	chr2:212352759-212352760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75018172	chr2:212352792-212352793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144689609	chr2:212352793-212352794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs79536373	chr2:212352794-212352795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188483695	chr2:212352803-212352804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112349206	chr2:212352834-212352835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573781814	chr2:212352858-212352859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75731114	chr2:212352865-212352866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562308853	chr2:212352894-212352895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527884031	chr2:212352912-212352913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7585464	chr2:212352958-212352959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368854240	chr2:212352977-212352978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564816646	chr2:212353005-212353006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533430480	chr2:212353041-212353042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs77462436	chr2:212353062-212353063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs57886952	chr2:212353081-212353082	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs529390108	chr2:212353133-212353134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs34940919	chr2:212353140-212353141	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs541642970	chr2:212353141-212353142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562563686	chr2:212353154-212353155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs534803021	chr2:212353161-212353162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs375383679	chr2:212353170-212353171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73069173	chr2:212353250-212353251	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs112965240	chr2:212353279-212353280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs7586077	chr2:212353299-212353300	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs557003766	chr2:212353325-212353326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573668677	chr2:212353375-212353376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542790357	chr2:212353391-212353392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553081544	chr2:212353392-212353393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530390360	chr2:212353438-212353439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572817134	chr2:212353478-212353479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184942811	chr2:212353495-212353496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs78569879	chr2:212353502-212353503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188719231	chr2:212353525-212353526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191626210	chr2:212353546-212353547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563391705	chr2:212353558-212353559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs375637990	chr2:212353575-212353576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76218832	chr2:212353576-212353577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549103644	chr2:212353615-212353616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148281900	chr2:212353628-212353629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs77754135	chr2:212353649-212353650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183876346	chr2:212353691-212353692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565823731	chr2:212353697-212353698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs571312254	chr2:212353698-212353699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs371941336	chr2:212353751-212353752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs35792033	chr2:212353761-212353762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537390206	chr2:212353796-212353797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550890573	chr2:212353826-212353827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	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
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	17661082	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	18990708	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212352200-212353000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:212352200-212353000	Enhancers	Brain Angular Gyrus	brain
3	chr2:212352400-212352800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:212352400-212352800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr2:212352400-212352800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:212352400-212352800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
7	chr2:212352400-212353000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:212352400-212353000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:212352400-212353000	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr2:212352400-212353200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:212352400-212353200	Enhancers	Brain Anterior Caudate	brain
12	chr2:212352400-212353200	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr2:212352400-212353800	Enhancers	Brain Substantia Nigra	brain
14	chr2:212352600-212353000	Enhancers	Brain Hippocampus Middle	brain
15	chr2:212352800-212353000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr2:212352800-212362200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:212353000-212363400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:212358600-212359200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr2:212358800-212359400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr2:212359200-212363200	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr2:212359400-212363200	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr2:212362000-212365400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr2:212362200-212362800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr2:212362200-212364000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:212362600-212363800	Enhancers	Brain Angular Gyrus	brain
26	chr2:212362800-212363200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr2:212362800-212363800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr2:212362800-212363800	Enhancers	Brain Hippocampus Middle	brain
29	chr2:212362800-212368600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:212363200-212363400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:212363200-212363800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr2:212363200-212363800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr2:212363200-212363800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr2:212363200-212364000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr2:212363200-212364000	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr2:212363200-212364000	Enhancers	Brain Cingulate Gyrus	brain
37	chr2:212363200-212364000	Enhancers	Brain Substantia Nigra	brain
38	chr2:212363400-212363600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr2:212363400-212363800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr2:212363400-212363800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
41	chr2:212363400-212363800	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr2:212363400-212363800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
43	chr2:212363400-212364000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr2:212363600-212363800	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr2:212363800-212364000	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr2:212363800-212364000	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr2:212364000-212364400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:212364000-212364400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr2:212364400-212364800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr2:212364400-212365200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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