Variant report

Variant	nsv874661
Chromosome Location	chr2:96334397-96459313
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:96394384-96394976	HepG2	liver:	n/a	n/a
2	BATF	chr2:96389586-96389891	GM12878	blood:	n/a	n/a
3	BATF	chr2:96401104-96401456	GM12878	blood:	n/a	n/a
4	BATF	chr2:96389629-96389835	GM12878	blood:	n/a	n/a
5	BATF	chr2:96373042-96373284	GM12878	blood:	n/a	chr2:96373152-96373163
6	BATF	chr2:96373017-96373229	GM12878	blood:	n/a	chr2:96373152-96373163
7	BCL11A	chr2:96401104-96401290	GM12878	blood:	n/a	n/a
8	BCL11A	chr2:96401015-96401259	GM12878	blood:	n/a	n/a
9	BCL11A	chr2:96442951-96443157	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:96394763-96394892	GM12878	blood:	n/a	n/a
11	CBX3	chr2:96432533-96432779	K562	blood:	n/a	n/a
12	CEBPB	chr2:96391404-96391735	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:96426837-96427246	IMR90	lung:	n/a	chr2:96427040-96427051
14	CEBPB	chr2:96394271-96395330	HepG2	liver:	n/a	chr2:96394419-96394430 chr2:96394419-96394432
15	CEBPB	chr2:96394709-96395335	K562	blood:	n/a	n/a
16	CEBPB	chr2:96394684-96394919	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:96426884-96427208	Hela-S3	cervix:	n/a	chr2:96427040-96427051
18	CEBPB	chr2:96394316-96394473	K562	blood:	n/a	chr2:96394419-96394430 chr2:96394419-96394432
19	CEBPB	chr2:96426902-96427182	MCF-7	breast:	n/a	chr2:96427040-96427051
20	CEBPB	chr2:96426939-96427088	HepG2	liver:	n/a	chr2:96427040-96427051
21	CEBPB	chr2:96352196-96352515	A549	lung:	n/a	chr2:96352336-96352349 chr2:96352338-96352349 chr2:96352336-96352347 chr2:96352336-96352349
22	CEBPB	chr2:96352290-96352412	HepG2	liver:	n/a	chr2:96352336-96352349 chr2:96352338-96352349 chr2:96352336-96352347 chr2:96352336-96352349
23	CEBPB	chr2:96394654-96395269	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr2:96352152-96352528	IMR90	lung:	n/a	chr2:96352336-96352349 chr2:96352338-96352349 chr2:96352336-96352347 chr2:96352336-96352349
25	CEBPB	chr2:96361449-96361668	K562	blood:	n/a	n/a
26	CEBPB	chr2:96353649-96353979	IMR90	lung:	n/a	n/a
27	CEBPB	chr2:96352306-96352520	A549	lung:	n/a	chr2:96352336-96352349 chr2:96352338-96352349 chr2:96352336-96352347 chr2:96352336-96352349
28	CEBPB	chr2:96352308-96352398	Hela-S3	cervix:	n/a	chr2:96352336-96352349 chr2:96352338-96352349 chr2:96352336-96352347 chr2:96352336-96352349
29	CEBPB	chr2:96352310-96352556	MCF-7	breast:	n/a	chr2:96352336-96352349 chr2:96352338-96352349 chr2:96352336-96352347 chr2:96352336-96352349
30	CEBPB	chr2:96394342-96395320	A549	lung:	n/a	chr2:96394419-96394430 chr2:96394419-96394432
31	CEBPB	chr2:96394289-96395327	IMR90	lung:	n/a	chr2:96394419-96394430 chr2:96394419-96394432
32	CTCF	chr2:96394666-96395029	A549	lung:	n/a	chr2:96394849-96394870 chr2:96394854-96394872
33	CTCF	chr2:96395260-96395410	GM12875	blood:	n/a	n/a
34	CTCF	chr2:96394780-96394930	GM12801	blood:	n/a	chr2:96394849-96394870 chr2:96394854-96394872
35	CTCF	chr2:96394920-96395070	HCT-116	colon:	n/a	n/a
36	CTCF	chr2:96394780-96394930	GM12875	blood:	n/a	chr2:96394849-96394870 chr2:96394854-96394872
37	CTCF	chr2:96394900-96395050	A549	lung:	n/a	n/a
38	CTCF	chr2:96441049-96441171	Spleen_OC	spleen:	n/a	chr2:96441089-96441107
39	CTCF	chr2:96441010-96441186	GM10266	blood:	n/a	chr2:96441089-96441107
40	CTCF	chr2:96429789-96429903	GM13976	blood:	n/a	chr2:96429822-96429840
41	CTCF	chr2:96394720-96394870	NHDF-neo	bronchial:	n/a	chr2:96394849-96394870
42	CTCF	chr2:96394680-96394830	HAc	cerebellar:	n/a	n/a
43	CTCF	chr2:96395220-96395370	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr2:96343740-96343888	Hela-S3	cervix:	n/a	chr2:96343803-96343816 chr2:96343801-96343819 chr2:96343802-96343818
45	CTCF	chr2:96430360-96430510	HepG2	liver:	n/a	n/a
46	CTCF	chr2:96394800-96394950	BJ	skin:	n/a	chr2:96394849-96394870 chr2:96394854-96394872
47	CTCF	chr2:96394740-96394890	AG09309	skin:	n/a	chr2:96394849-96394870 chr2:96394854-96394872
48	CTCF	chr2:96394684-96394981	K562	blood:	n/a	chr2:96394849-96394870 chr2:96394854-96394872
49	CTCF	chr2:96394422-96395136	A549	lung:	n/a	chr2:96394849-96394870 chr2:96394854-96394872
50	CTCF	chr2:96426704-96426806	Gliobla	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:96348691-96348741	Jurkat	blood:	n/a
2	chr2:96348691-96348741	NT2-D1	testis:	n/a
3	chr2:96348691-96348741	Jurkat	blood:	n/a
4	chr2:96348691-96348741	NT2-D1	testis:	n/a
5	chr2:96427173-96427223	SAEC	small airway:	n/a
6	chr2:96458247-96458297	HPAEpiC	pulmonary alveolar:	n/a
7	chr2:96348691-96348741	GM12878	blood:	n/a
8	chr2:96458247-96458297	H1-hESC	embryonic stem cell:	embryo
9	chr2:96427173-96427223	PFSK-1	brain:	n/a
10	chr2:96427173-96427223	GM19239	blood:	n/a
11	chr2:96427173-96427223	GM06990	blood:	n/a
12	chr2:96348691-96348741	BE2_C	brain:	n/a
13	chr2:96458247-96458297	NB4	blood:	n/a
14	chr2:96427173-96427223	A549	lung:	n/a
15	chr2:96427173-96427223	NHDF-neo	bronchial:	n/a
16	chr2:96458247-96458297	HCPEpiC	choroid plexus:	n/a
17	chr2:96458247-96458297	SK-N-SH_RA	brain:	n/a
18	chr2:96427173-96427223	GM12891	blood:	n/a
19	chr2:96458247-96458297	ovcar-3	ovarian:	n/a
20	chr2:96427173-96427223	AG04449	skin:	fetal
21	chr2:96427173-96427223	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:96458247-96458297	HRCEpiC	kidney:	n/a
23	chr2:96348691-96348741	A549	lung:	n/a
24	chr2:96348691-96348741	SAEC	small airway:	n/a
25	chr2:96348691-96348741	U87	brain:	n/a
26	chr2:96427173-96427223	HUVEC	blood vessel:	n/a
27	chr2:96348691-96348741	AG09309	skin:	n/a
28	chr2:96427173-96427223	HCPEpiC	choroid plexus:	n/a
29	chr2:96348691-96348741	GM12892	blood:	n/a
30	chr2:96458247-96458297	GM06990	blood:	n/a
31	chr2:96458247-96458297	MCF10A-Er-Src	breast:	n/a
32	chr2:96427173-96427223	AG09319	gingival:	n/a
33	chr2:96427173-96427223	HNPCEpiC	eye:	n/a
34	chr2:96427173-96427223	SK-N-SH_RA	brain:	n/a
35	chr2:96348691-96348741	Hela-S3	cervix:	n/a
36	chr2:96427173-96427223	SK-N-MC	brain:	n/a
37	chr2:96427173-96427223	HRPEpiC	eye:	n/a
38	chr2:96458247-96458297	CMK	blood:	n/a
39	chr2:96427173-96427223	PANC-1	pancreas:	n/a
40	chr2:96427173-96427223	SK-N-SH	brain:	n/a
41	chr2:96348691-96348741	HAEpiC	amniotic membrane:	n/a
42	chr2:96348691-96348741	NH-A	brain:	n/a
43	chr2:96458247-96458297	RPTEC	kidney:	n/a
44	chr2:96458247-96458297	HCM	heart:	n/a
45	chr2:96348691-96348741	HCF	heart:	n/a
46	chr2:96348691-96348741	PFSK-1	brain:	n/a
47	chr2:96427173-96427223	HL-60	blood:	n/a
48	chr2:96427173-96427223	AG10803	skin:	n/a
49	chr2:96458247-96458297	Hela-S3	cervix:	n/a
50	chr2:96348691-96348741	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:96054639..96055198-chr2:96394784..96395584,2	K562	blood:
2	chr2:96406055..96406842-chr2:114139694..114140465,2	MCF-7	breast:
3	chr2:96362570..96365117-chr2:96367359..96369981,2	MCF-7	breast:
4	chr2:96054886..96055732-chr2:96394556..96395496,2	MCF-7	breast:
5	chr2:96079865..96080377-chr2:96394455..96395330,2	K562	blood:
6	chr2:96011050..96011912-chr2:96394384..96395342,2	MCF-7	breast:
7	chr2:96054634..96055511-chr2:96394406..96395211,2	MCF-7	breast:
8	chr2:96362570..96365117-chr2:96367359..96369981,2	MCF-7	breast:
9	chr13:60970490..60971024-chr2:96378837..96379342,2	NB4	blood:
10	chr2:96058513..96059040-chr2:96394487..96395166,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM43-1	chr2:96333665-96334463	XLOC_001575
2	lnc-ANKRD36C-2	chr2:96379286-96379320	XLOC_002206
3	lnc-ANKRD36C-2	chr2:96383793-96384234	XLOC_002206
4	lnc-TRIM43-1	chr2:96333664-96334497	NONHSAT072506

Variant related genes	Relation type
ENSG00000237510	TF binding region
ENSG00000237510	CpG island
ENSG00000083544	chromatin interactions
ENSG00000248821	chromatin interactions

Extended variants
information (count: 2513 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2513 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10515920	chr2:96334397-96334398	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182900043	chr2:96334416-96334417	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs556751255	chr2:96334448-96334449	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs573794483	chr2:96334489-96334490	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs188402693	chr2:96334511-96334512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553131093	chr2:96334527-96334528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142667721	chr2:96334531-96334532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144878942	chr2:96334561-96334562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373602937	chr2:96334563-96334564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190645749	chr2:96334572-96334573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575207159	chr2:96334594-96334595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182949272	chr2:96334627-96334628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34010054	chr2:96334690-96334691	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs530187754	chr2:96334691-96334692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540516816	chr2:96334707-96334708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560727009	chr2:96334789-96334790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187711298	chr2:96334790-96334791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192555195	chr2:96334823-96334824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552854473	chr2:96334824-96334825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185081437	chr2:96334870-96334871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530481464	chr2:96334892-96334893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187441069	chr2:96334926-96334927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192288192	chr2:96334972-96334973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564145973	chr2:96334995-96334996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536338974	chr2:96334996-96334997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552903226	chr2:96335002-96335003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184599019	chr2:96335035-96335036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs531402735	chr2:96335036-96335037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35743343	chr2:96335037-96335038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558398358	chr2:96335047-96335048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575177430	chr2:96335056-96335057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544305979	chr2:96335086-96335087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138833730	chr2:96335088-96335089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369864340	chr2:96335124-96335125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560523052	chr2:96335203-96335204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141938255	chr2:96335256-96335257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546533989	chr2:96335277-96335278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189920469	chr2:96335315-96335316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111409505	chr2:96335426-96335427	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs532041752	chr2:96335458-96335459	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs550346841	chr2:96335487-96335488	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs192146150	chr2:96335501-96335502	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs529754827	chr2:96335536-96335537	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs546649453	chr2:96335539-96335540	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs566347515	chr2:96335542-96335543	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs139317098	chr2:96335559-96335560	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs537009709	chr2:96335562-96335563	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs558309999	chr2:96335603-96335604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs117911784	chr2:96335841-96335842	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs538132301	chr2:96335848-96335849	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
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
Autism	17483303	CNVD
Medulloblastoma	20607354	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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Neuroblastoma	18574593	CNVD
Hepatocellular carcinoma	16750200	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
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Epilepsy	22083797	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:723 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96328200-96336400	Weak transcription	Right Atrium	heart
2	chr2:96330000-96334600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr2:96330000-96334800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr2:96330200-96334600	Weak transcription	Primary B cells from peripheral blood	blood
5	chr2:96330400-96334600	Weak transcription	Primary B cells from cord blood	blood
6	chr2:96330600-96334600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:96330600-96336600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:96331800-96338800	Enhancers	Fetal Thymus	thymus
9	chr2:96332000-96335000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr2:96333200-96335200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr2:96333400-96336800	Enhancers	Dnd41	blood
12	chr2:96333400-96338000	Enhancers	Thymus	Thymus
13	chr2:96333600-96334800	Enhancers	Lung	lung
14	chr2:96333600-96335800	Weak transcription	HSMMtube	muscle
15	chr2:96333800-96335400	Weak transcription	HSMM	muscle
16	chr2:96333800-96335800	Weak transcription	Fetal Muscle Leg	muscle
17	chr2:96334000-96336000	Weak transcription	NHEK	skin
18	chr2:96334200-96334600	Weak transcription	NHDF-Ad	bronchial
19	chr2:96334200-96335800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr2:96334200-96336200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr2:96334200-96336400	Weak transcription	HMEC	breast
22	chr2:96334400-96335200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr2:96334400-96335600	Enhancers	Primary T cells from cord blood	blood
24	chr2:96334600-96335600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr2:96334600-96336600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:96334600-96336800	Enhancers	Primary B cells from peripheral blood	blood
27	chr2:96334600-96337000	Enhancers	Primary B cells from cord blood	blood
28	chr2:96334600-96337400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr2:96334600-96338600	Enhancers	NHDF-Ad	bronchial
30	chr2:96334800-96335600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr2:96335000-96336200	Enhancers	Primary hematopoietic stem cells	blood
32	chr2:96335200-96335400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr2:96335200-96335600	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr2:96335200-96336800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr2:96335200-96337200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr2:96335200-96337200	Enhancers	Osteobl	bone
37	chr2:96335200-96337400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr2:96335200-96338000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr2:96335400-96335600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr2:96335400-96335600	Enhancers	Adipose Nuclei	Adipose
41	chr2:96335400-96336400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr2:96335400-96336800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr2:96335400-96336800	Enhancers	HSMM	muscle
44	chr2:96335400-96336800	Enhancers	NH-A	brain
45	chr2:96335400-96337000	Enhancers	NHLF	lung
46	chr2:96335400-96340600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr2:96335600-96335800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr2:96335600-96336200	Weak transcription	Adipose Nuclei	Adipose
49	chr2:96335800-96336000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr2:96335800-96337000	Enhancers	HSMMtube	muscle

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