Variant report

Variant	nsv1007408
Chromosome Location	chr2:77235194-77255152
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:77)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:77 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr2:77245313-77245520	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr2:77237338-77237675	A549	lung:	n/a	chr2:77237500-77237511
3	CEBPB	chr2:77237329-77237636	Hela-S3	cervix:	n/a	chr2:77237500-77237511
4	CEBPB	chr2:77237322-77237686	HepG2	liver:	n/a	chr2:77237500-77237511
5	CEBPB	chr2:77248848-77249023	HepG2	liver:	n/a	chr2:77248892-77248903
6	CEBPB	chr2:77236178-77236760	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr2:77237328-77237684	H1-hESC	embryonic stem cell:	n/a	chr2:77237500-77237511
8	CEBPB	chr2:77237318-77237676	IMR90	lung:	n/a	chr2:77237500-77237511
9	CEBPB	chr2:77237433-77237528	K562	blood:	n/a	chr2:77237500-77237511
10	E2F4	chr2:77247091-77247420	MCF10A-Er-Src	breast:	n/a	n/a
11	E2F4	chr2:77255128-77255343	MCF10A-Er-Src	breast:	n/a	n/a
12	E2F4	chr2:77236140-77236316	MCF10A-Er-Src	breast:	n/a	n/a
13	EP300	chr2:77236341-77236761	Hela-S3	cervix:	n/a	n/a
14	FOS	chr2:77236368-77236751	MCF10A-Er-Src	breast:	n/a	chr2:77236560-77236571
15	FOS	chr2:77236151-77236796	HUVEC	blood vessel:	n/a	chr2:77236560-77236571
16	FOS	chr2:77236285-77236839	MCF10A-Er-Src	breast:	n/a	chr2:77236560-77236571
17	FOS	chr2:77236315-77236740	MCF10A-Er-Src	breast:	n/a	chr2:77236560-77236571
18	FOS	chr2:77234898-77235259	HUVEC	blood vessel:	n/a	chr2:77235070-77235078 chr2:77234929-77234941 chr2:77235071-77235078
19	FOS	chr2:77236177-77236755	MCF10A-Er-Src	breast:	n/a	chr2:77236560-77236571
20	FOXA1	chr2:77240584-77240881	HepG2	liver:	n/a	n/a
21	FOXA1	chr2:77237373-77237586	HepG2	liver:	n/a	n/a
22	FOXA1	chr2:77240560-77240952	HepG2	liver:	n/a	n/a
23	FOXA1	chr2:77240614-77241042	HepG2	liver:	n/a	n/a
24	GATA2	chr2:77234343-77235327	HUVEC	blood vessel:	n/a	chr2:77235071-77235080
25	GATA3	chr2:77245672-77245863	SH-SY5Y	brain:	n/a	chr2:77245740-77245761
26	GATA3	chr2:77234769-77235278	SH-SY5Y	brain:	n/a	chr2:77235071-77235080
27	GATA3	chr2:77235519-77235858	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr2:77240639-77240941	T-47D	breast:	n/a	n/a
29	GATA3	chr2:77245360-77245936	MCF-7	breast:	n/a	chr2:77245634-77245643 chr2:77245740-77245761
30	GATA3	chr2:77240673-77240869	T-47D	breast:	n/a	n/a
31	JUN	chr2:77237425-77237431	H1-hESC	embryonic stem cell:	n/a	n/a
32	JUN	chr2:77236365-77236756	Hela-S3	cervix:	n/a	n/a
33	JUN	chr2:77236399-77236710	HepG2	liver:	n/a	n/a
34	JUN	chr2:77236379-77236732	HUVEC	blood vessel:	n/a	n/a
35	JUND	chr2:77236211-77236738	H1-hESC	embryonic stem cell:	n/a	chr2:77236560-77236571
36	JUND	chr2:77247557-77247590	H1-hESC	embryonic stem cell:	n/a	n/a
37	JUND	chr2:77236195-77236898	SK-N-SH	brain:	n/a	chr2:77236560-77236571
38	JUND	chr2:77248456-77248584	HepG2	liver:	n/a	chr2:77248514-77248525
39	JUND	chr2:77236099-77236791	Hela-S3	cervix:	n/a	chr2:77236560-77236571
40	JUND	chr2:77236373-77236739	HepG2	liver:	n/a	chr2:77236560-77236571
41	KAP1	chr2:77235863-77236934	U2OS	brain:	n/a	n/a
42	KAP1	chr2:77235800-77236864	HEK293	kidney:	n/a	n/a
43	MAFK	chr2:77248591-77248708	HepG2	liver:	n/a	n/a
44	MAFK	chr2:77248540-77248628	HepG2	liver:	n/a	n/a
45	MAZ	chr2:77248962-77248975	HepG2	liver:	n/a	n/a
46	MYC	chr2:77236427-77236627	MCF10A-Er-Src	breast:	n/a	n/a
47	NANOG	chr2:77245284-77245683	H1-hESC	embryonic stem cell:	n/a	chr2:77245404-77245418
48	NFYB	chr2:77235267-77235442	GM12878	blood:	n/a	n/a
49	NR2F2	chr2:77245454-77245874	MCF-7	breast:	n/a	n/a
50	POLR2A	chr2:77235589-77236590	H1-neurons	neurons:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:77235218-77235268	A549	lung:	n/a
2	chr2:77235218-77235268	HL-60	blood:	n/a
3	chr2:77235218-77235268	HepG2	liver:	n/a
4	chr2:77235218-77235268	HRCEpiC	kidney:	n/a
5	chr2:77235218-77235268	NH-A	brain:	n/a
6	chr2:77235218-77235268	NHBE	bronchial:	n/a
7	chr2:77235218-77235268	AG10803	skin:	n/a
8	chr2:77235218-77235268	PrEC	prostate:	n/a
9	chr2:77235218-77235268	HEK293	kidney:	embryo
10	chr2:77235218-77235268	GM12878	blood:	n/a
11	chr2:77235218-77235268	RPTEC	kidney:	n/a
12	chr2:77235218-77235268	SK-N-MC	brain:	n/a
13	chr2:77235218-77235268	U87	brain:	n/a
14	chr2:77235218-77235268	AoSMC	blood vessel:	n/a
15	chr2:77235218-77235268	Jurkat	blood:	n/a
16	chr2:77235218-77235268	ProgFib	skin:	n/a
17	chr2:77235218-77235268	HIPEpiC	eye:	n/a
18	chr2:77235218-77235268	SKMC	muscle:	n/a
19	chr2:77235218-77235268	HUVEC	blood vessel:	n/a
20	chr2:77235218-77235268	PFSK-1	brain:	n/a
21	chr2:77235218-77235268	AG09309	skin:	n/a
22	chr2:77235218-77235268	HAEpiC	amniotic membrane:	n/a
23	chr2:77235218-77235268	HCM	heart:	n/a
24	chr2:77235218-77235268	HRPEpiC	eye:	n/a
25	chr2:77235218-77235268	HCT-116	colon:	n/a
26	chr2:77235218-77235268	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:77235218-77235268	GM12891	blood:	n/a
28	chr2:77235218-77235268	T-47D	breast:	n/a
29	chr2:77235218-77235268	SK-N-SH_RA	brain:	n/a
30	chr2:77235218-77235268	CMK	blood:	n/a
31	chr2:77235218-77235268	MCF-7	breast:	n/a
32	chr2:77235218-77235268	BE2_C	brain:	n/a
33	chr2:77235218-77235268	AG09319	gingival:	n/a
34	chr2:77235218-77235268	Hepatocyte	liver:	n/a
35	chr2:77235218-77235268	HMEC	breast:	n/a
36	chr2:77235218-77235268	HNPCEpiC	eye:	n/a
37	chr2:77235218-77235268	HRE	kidney:	n/a
38	chr2:77235218-77235268	LNCaP	prostate:	n/a
39	chr2:77235218-77235268	HCPEpiC	choroid plexus:	n/a
40	chr2:77235218-77235268	MCF10A-Er-Src	breast:	n/a
41	chr2:77235218-77235268	NHDF-neo	bronchial:	n/a
42	chr2:77235218-77235268	H1-hESC	embryonic stem cell:	embryo
43	chr2:77235218-77235268	NT2-D1	testis:	n/a
44	chr2:77235218-77235268	Hela-S3	cervix:	n/a
45	chr2:77235218-77235268	AG04450	lung:	fetal
46	chr2:77235218-77235268	HEEpiC	esophagus:	n/a
47	chr2:77235218-77235268	SK-N-SH	brain:	n/a
48	chr2:77235218-77235268	PANC-1	pancreas:	n/a
49	chr2:77235218-77235268	K562	blood:	n/a
50	chr2:77235218-77235268	NB4	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:77243462..77244011-chr5:75510913..75511675,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPL19-4	chr2:77236150-77236917	ENSG00000234653.1
2	lnc-MRPL19-4	chr2:77236150-77236914	NR_110284

No data

Variant related genes	Relation type
ENSG00000211984	TF binding region
ENSG00000211984	CpG island

Extended variants
information (count: 923 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:923 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62170867	chr2:77235200-77235201	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs1446704	chr2:77235219-77235220	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs562130986	chr2:77235222-77235223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574063312	chr2:77235238-77235239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527976388	chr2:77235240-77235241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs377569469	chr2:77235243-77235244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549357590	chr2:77235249-77235250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144411766	chr2:77235255-77235256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531724737	chr2:77235264-77235265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs13396539	chr2:77235268-77235269	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs559970101	chr2:77235279-77235280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1446703	chr2:77235311-77235312	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs13384774	chr2:77235396-77235397	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs148786085	chr2:77235453-77235454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565884389	chr2:77235454-77235455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536526660	chr2:77235459-77235460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552975036	chr2:77235462-77235463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1446702	chr2:77235470-77235471	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs62170868	chr2:77235472-77235473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs17013595	chr2:77235523-77235524	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs550281263	chr2:77235561-77235562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs386647560	chr2:77235582-77235583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115931976	chr2:77235584-77235585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576780805	chr2:77235591-77235592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540709961	chr2:77235612-77235613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75379132	chr2:77235615-77235616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572677685	chr2:77235620-77235621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186829419	chr2:77235715-77235716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561168030	chr2:77235732-77235733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372342310	chr2:77235747-77235748	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531744892	chr2:77235749-77235750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563876035	chr2:77235782-77235783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192724538	chr2:77235818-77235819	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs141523071	chr2:77235842-77235843	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs565079591	chr2:77235852-77235853	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs72912512	chr2:77235862-77235863	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs147502003	chr2:77235897-77235898	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs566052186	chr2:77235898-77235899	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs536173863	chr2:77235917-77235918	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs139571764	chr2:77235922-77235923	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs114958140	chr2:77235923-77235924	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs183615794	chr2:77235927-77235928	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs558773464	chr2:77235928-77235929	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs145164656	chr2:77235931-77235932	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs147582438	chr2:77235946-77235947	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs552729054	chr2:77235965-77235966	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs547812016	chr2:77235995-77235996	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs574339638	chr2:77235999-77236000	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs188554403	chr2:77236032-77236033	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs193240160	chr2:77236053-77236054	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	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
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Epilepsy	22083797	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77231600-77235800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:77232000-77245600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:77232600-77238200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:77232800-77238000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr2:77233600-77235200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr2:77233600-77237200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr2:77233800-77235800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr2:77233800-77236000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr2:77233800-77236800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr2:77233800-77237000	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr2:77233800-77237000	Enhancers	HUVEC	blood vessel
12	chr2:77234000-77235600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:77234000-77235800	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr2:77234000-77237600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr2:77234200-77239000	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr2:77234400-77236200	Enhancers	Brain Germinal Matrix	brain
17	chr2:77234400-77238200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr2:77234600-77235200	Enhancers	Brain Anterior Caudate	brain
19	chr2:77234600-77237000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr2:77234600-77237600	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr2:77234800-77235600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr2:77234800-77235800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr2:77234800-77236000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr2:77234800-77236600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr2:77235000-77235200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr2:77235000-77237800	Enhancers	Fetal Brain Male	brain
27	chr2:77235200-77235600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr2:77235200-77235600	Weak transcription	Brain Anterior Caudate	brain
29	chr2:77235200-77236800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr2:77235600-77236000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr2:77235600-77236000	Enhancers	Fetal Brain Female	brain
32	chr2:77235600-77236800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr2:77235600-77236800	Enhancers	Brain Anterior Caudate	brain
34	chr2:77235600-77237000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr2:77235800-77236000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr2:77235800-77236400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr2:77235800-77236400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr2:77235800-77237000	Enhancers	H1 Cell Line	embryonic stem cell
39	chr2:77235800-77237000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr2:77236000-77236400	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr2:77236000-77236600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr2:77236000-77239600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr2:77236200-77236400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr2:77236200-77236400	Enhancers	Fetal Lung	lung
45	chr2:77236200-77237000	Enhancers	NH-A	brain
46	chr2:77236400-77236800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr2:77236400-77236800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr2:77236400-77237400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:77236400-77239600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:77236400-77240200	Weak transcription	Fetal Lung	lung

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