Variant report

Variant	nsv1051913
Chromosome Location	chr12:29741676-29770807
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:260)
CpG islands
(count:183)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:29744165-29744740	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr12:29744198-29744221	GM12878	blood:	n/a	n/a
3	CEBPB	chr12:29753295-29753499	HepG2	liver:	n/a	chr12:29753415-29753426 chr12:29753415-29753424 chr12:29753413-29753426 chr12:29753415-29753426 chr12:29753413-29753424 chr12:29753415-29753424 chr12:29753415-29753424 chr12:29753415-29753424
4	CEBPB	chr12:29744605-29744953	IMR90	lung:	n/a	chr12:29744782-29744793
5	CEBPB	chr12:29753307-29753530	A549	lung:	n/a	chr12:29753415-29753426 chr12:29753415-29753424 chr12:29753413-29753426 chr12:29753415-29753426 chr12:29753413-29753424 chr12:29753415-29753424 chr12:29753415-29753424 chr12:29753415-29753424
6	CEBPB	chr12:29744659-29744952	HepG2	liver:	n/a	chr12:29744782-29744793
7	CEBPB	chr12:29753272-29753584	IMR90	lung:	n/a	chr12:29753415-29753426 chr12:29753415-29753424 chr12:29753413-29753426 chr12:29753415-29753426 chr12:29753413-29753424 chr12:29753415-29753424 chr12:29753415-29753424 chr12:29753415-29753424
8	CEBPB	chr12:29744706-29744884	A549	lung:	n/a	chr12:29744782-29744793
9	CEBPB	chr12:29756420-29756769	IMR90	lung:	n/a	n/a
10	CEBPB	chr12:29744252-29744973	H1-hESC	embryonic stem cell:	n/a	chr12:29744258-29744266 chr12:29744782-29744793
11	CTCF	chr12:29765100-29765250	HMEC	breast:	n/a	n/a
12	CTCF	chr12:29744100-29744250	GM12870	blood:	n/a	n/a
13	CTCF	chr12:29744080-29744230	GM12868	blood:	n/a	n/a
14	CTCF	chr12:29744160-29744310	MCF-7	breast:	n/a	n/a
15	CTCF	chr12:29765140-29765290	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr12:29744140-29744290	HPF	lung:	n/a	n/a
17	CTCF	chr12:29744153-29744311	MCF-7	breast:	n/a	n/a
18	CTCF	chr12:29763540-29763690	BE2_C	brain:	n/a	n/a
19	CTCF	chr12:29744140-29744290	HMEC	breast:	n/a	n/a
20	CTCF	chr12:29744360-29744510	GM12867	blood:	n/a	n/a
21	CTCF	chr12:29744160-29744310	AG04449	skin:	n/a	n/a
22	CTCF	chr12:29744041-29744379	IMR90	lung:	n/a	n/a
23	CTCF	chr12:29765040-29765190	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr12:29744140-29744290	HCFaa	heart:	n/a	n/a
25	CTCF	chr12:29744140-29744290	SAEC	small airway:	n/a	n/a
26	CTCF	chr12:29744052-29744370	K562	blood:	n/a	n/a
27	CTCF	chr12:29765040-29765190	HMF	breast:	n/a	n/a
28	CTCF	chr12:29744120-29744270	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr12:29744186-29744286	GM10266	blood:	n/a	n/a
30	CTCF	chr12:29744100-29744250	HAc	cerebellar:	n/a	n/a
31	CTCF	chr12:29744180-29744330	K562	blood:	n/a	n/a
32	CTCF	chr12:29765060-29765210	BE2_C	brain:	n/a	n/a
33	CTCF	chr12:29744138-29744304	K562	blood:	n/a	n/a
34	CTCF	chr12:29763280-29763430	BE2_C	brain:	n/a	n/a
35	CTCF	chr12:29744100-29744250	GM12878	blood:	n/a	n/a
36	CTCF	chr12:29744160-29744310	GM12865	blood:	n/a	n/a
37	CTCF	chr12:29744160-29744310	HFF-Myc	foreskin:	n/a	n/a
38	CTCF	chr12:29744048-29744385	GM12878	blood:	n/a	n/a
39	CTCF	chr12:29744080-29744230	HVMF	connective:	n/a	n/a
40	CTCF	chr12:29744160-29744310	HMF	breast:	n/a	n/a
41	CTCF	chr12:29744140-29744290	GM12873	blood:	n/a	n/a
42	CTCF	chr12:29744140-29744290	HRE	kidney:	n/a	n/a
43	CTCF	chr12:29763460-29763610	GM12865	blood:	n/a	n/a
44	CTCF	chr12:29765080-29765230	AG09319	gingival:	n/a	n/a
45	CTCF	chr12:29744140-29744290	Caco-2	colon:	n/a	n/a
46	CTCF	chr12:29744140-29744290	GM12872	blood:	n/a	n/a
47	CTCF	chr12:29744147-29744321	GM19238	blood:	n/a	n/a
48	CTCF	chr12:29744120-29744270	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr12:29765148-29765223	GM12878	blood:	n/a	n/a
50	CTCF	chr12:29763600-29763750	GM12873	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:29763500-29763550	H1-hESC	embryonic stem cell:	embryo
2	chr12:29770547-29770597	T-47D	breast:	n/a
3	chr12:29770547-29770597	U87	brain:	n/a
4	chr12:29744537-29744587	GM06990	blood:	n/a
5	chr12:29770547-29770597	HepG2	liver:	n/a
6	chr12:29763500-29763550	PANC-1	pancreas:	n/a
7	chr12:29763500-29763550	CMK	blood:	n/a
8	chr12:29763500-29763550	HMEC	breast:	n/a
9	chr12:29744537-29744587	HCM	heart:	n/a
10	chr12:29763500-29763550	Jurkat	blood:	n/a
11	chr12:29770547-29770597	GM12892	blood:	n/a
12	chr12:29770547-29770597	HRE	kidney:	n/a
13	chr12:29763500-29763550	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:29744537-29744587	AG09309	skin:	n/a
15	chr12:29744537-29744587	GM12891	blood:	n/a
16	chr12:29763500-29763550	ECC-1	luminal epithelium:	n/a
17	chr12:29770547-29770597	HPAEpiC	pulmonary alveolar:	n/a
18	chr12:29763500-29763550	HRE	kidney:	n/a
19	chr12:29744537-29744587	LNCaP	prostate:	n/a
20	chr12:29770547-29770597	HEEpiC	esophagus:	n/a
21	chr12:29744537-29744587	Caco-2	colon:	n/a
22	chr12:29763500-29763550	GM19239	blood:	n/a
23	chr12:29770547-29770597	PANC-1	pancreas:	n/a
24	chr12:29744537-29744587	HAEpiC	amniotic membrane:	n/a
25	chr12:29744537-29744587	HCT-116	colon:	n/a
26	chr12:29744537-29744587	NB4	blood:	n/a
27	chr12:29744537-29744587	MCF-7	breast:	n/a
28	chr12:29763500-29763550	MCF10A-Er-Src	breast:	n/a
29	chr12:29744537-29744587	IMR90	lung:	fetal
30	chr12:29763500-29763550	U87	brain:	n/a
31	chr12:29770547-29770597	HCT-116	colon:	n/a
32	chr12:29763500-29763550	LNCaP	prostate:	n/a
33	chr12:29770547-29770597	HAEpiC	amniotic membrane:	n/a
34	chr12:29744537-29744587	AG04450	lung:	fetal
35	chr12:29744537-29744587	SK-N-MC	brain:	n/a
36	chr12:29763500-29763550	NT2-D1	testis:	n/a
37	chr12:29763500-29763550	AoSMC	blood vessel:	n/a
38	chr12:29744537-29744587	ovcar-3	ovarian:	n/a
39	chr12:29770547-29770597	RPTEC	kidney:	n/a
40	chr12:29763500-29763550	HEK293	kidney:	embryo
41	chr12:29770547-29770597	HEK293	kidney:	embryo
42	chr12:29770547-29770597	Hela-S3	cervix:	n/a
43	chr12:29763500-29763550	Hepatocyte	liver:	n/a
44	chr12:29744537-29744587	SAEC	small airway:	n/a
45	chr12:29770547-29770597	LNCaP	prostate:	n/a
46	chr12:29763500-29763550	MCF-7	breast:	n/a
47	chr12:29744537-29744587	HRPEpiC	eye:	n/a
48	chr12:29744537-29744587	ProgFib	skin:	n/a
49	chr12:29763500-29763550	ovcar-3	ovarian:	n/a
50	chr12:29763500-29763550	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:29764406..29766975-chr12:29770947..29773354,2	MCF-7	breast:
2	chr12:29760132..29762663-chr12:29763281..29765764,2	MCF-7	breast:
3	chr12:29742455..29743103-chr17:80250455..80251110,2	NB4	blood:
4	chr12:29761123..29765125-chr12:29765200..29767546,3	K562	blood:
5	chr12:29761123..29763974-chr12:29765372..29767546,2	K562	blood:
6	chr12:29760132..29762663-chr12:29763281..29765764,2	MCF-7	breast:
7	chr12:29765447..29767500-chr12:29770091..29771858,2	MCF-7	breast:
8	chr12:29765447..29767500-chr12:29770091..29771858,2	MCF-7	breast:
9	chr12:29766099..29768378-chr12:29772903..29775657,3	MCF-7	breast:

No data

Variant related genes	Relation type
TMTC1	TF binding region
TMTC1	CpG island
ENSG00000133687	chromatin interactions
ENSG00000265692	chromatin interactions

Extended variants
information (count: 1129 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1129 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35832930	chr12:29741709-29741710	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs536015410	chr12:29741723-29741724	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs11050309	chr12:29741726-29741727	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs146277776	chr12:29741742-29741743	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs188284093	chr12:29741828-29741829	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs191235387	chr12:29741849-29741850	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs557955465	chr12:29741889-29741890	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs182346927	chr12:29741894-29741895	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs556627921	chr12:29741905-29741906	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs552745711	chr12:29741941-29741942	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs2350532	chr12:29741964-29741965	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs2081429	chr12:29742039-29742040	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs115138844	chr12:29742041-29742042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs117206633	chr12:29742052-29742053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543680855	chr12:29742053-29742054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs139358834	chr12:29742086-29742087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532336008	chr12:29742093-29742094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547393235	chr12:29742115-29742116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187648652	chr12:29742156-29742157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113863340	chr12:29742216-29742217	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77649201	chr12:29742305-29742306	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548419119	chr12:29742363-29742364	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192633387	chr12:29742385-29742386	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370070618	chr12:29742414-29742415	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73266079	chr12:29742419-29742420	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs4505145	chr12:29742450-29742451	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs570761606	chr12:29742524-29742525	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs185747905	chr12:29742542-29742543	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs542860507	chr12:29742561-29742562	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs552922569	chr12:29742563-29742564	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs568000333	chr12:29742607-29742608	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs116288689	chr12:29742672-29742673	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs189877351	chr12:29742675-29742676	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs147100402	chr12:29742694-29742695	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs73266080	chr12:29742706-29742707	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs558781228	chr12:29742729-29742730	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs577120151	chr12:29742743-29742744	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs77392560	chr12:29742753-29742754	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs559675795	chr12:29742756-29742757	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551701119	chr12:29742835-29742836	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs193156302	chr12:29742854-29742855	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs531918101	chr12:29742856-29742857	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs542271800	chr12:29742863-29742864	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs550041264	chr12:29742887-29742888	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs7311193	chr12:29742895-29742896	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs184581633	chr12:29742921-29742922	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs570699859	chr12:29742970-29742971	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs528378494	chr12:29742982-29742983	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs11421471	chr12:29743116-29743117	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs199947565	chr12:29743117-29743118	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	17133270	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29709800-29756200	Weak transcription	HMEC	breast
2	chr12:29713200-29742600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:29716200-29764800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr12:29720200-29743600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr12:29726000-29751400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr12:29729400-29744000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:29731000-29742600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr12:29731800-29769600	Weak transcription	Hela-S3	cervix
9	chr12:29735400-29745800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr12:29735800-29742400	Weak transcription	NHDF-Ad	bronchial
11	chr12:29736000-29742400	Weak transcription	HSMMtube	muscle
12	chr12:29736000-29743400	Weak transcription	Fetal Muscle Trunk	muscle
13	chr12:29736000-29744200	Weak transcription	Brain Hippocampus Middle	brain
14	chr12:29736000-29744200	Weak transcription	Right Atrium	heart
15	chr12:29736000-29752200	Weak transcription	HSMM	muscle
16	chr12:29736800-29742400	Weak transcription	NHLF	lung
17	chr12:29736800-29762800	Weak transcription	Fetal Stomach	stomach
18	chr12:29737000-29742400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr12:29737000-29742400	Weak transcription	Fetal Muscle Leg	muscle
20	chr12:29737000-29742400	Weak transcription	Lung	lung
21	chr12:29737000-29743200	Weak transcription	Fetal Heart	heart
22	chr12:29737000-29744200	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr12:29737000-29748400	Weak transcription	Spleen	Spleen
24	chr12:29737200-29742000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr12:29737200-29742200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr12:29737200-29742200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr12:29737200-29742400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr12:29737200-29742800	Weak transcription	Left Ventricle	heart
29	chr12:29737200-29744000	Weak transcription	Adipose Nuclei	Adipose
30	chr12:29737200-29744200	Weak transcription	Ovary	ovary
31	chr12:29737200-29744200	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr12:29737200-29746800	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr12:29737200-29748400	Weak transcription	Stomach Smooth Muscle	stomach
34	chr12:29737200-29761800	Weak transcription	Right Ventricle	heart
35	chr12:29737200-29762400	Weak transcription	Colon Smooth Muscle	Colon
36	chr12:29737200-29762800	Weak transcription	Psoas Muscle	Psoas
37	chr12:29740000-29742400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr12:29741000-29748200	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr12:29741400-29742000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr12:29741400-29742200	Weak transcription	Gastric	stomach
41	chr12:29741400-29742400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr12:29742000-29742400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr12:29742000-29742600	Weak transcription	Aorta	Aorta
44	chr12:29742000-29743600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr12:29742200-29742400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr12:29742200-29743400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr12:29742200-29743400	Enhancers	Fetal Lung	lung
48	chr12:29742200-29746000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr12:29742400-29742600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr12:29742400-29742600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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