Variant report

Variant	esv1796867
Chromosome Location	chr12:29501941-29524159
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:62)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:62 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr12:29518395-29518610	HepG2	liver:	n/a	n/a
2	CEBPB	chr12:29503029-29503287	A549	lung:	n/a	n/a
3	CEBPB	chr12:29504615-29504900	K562	blood:	n/a	n/a
4	CEBPB	chr12:29514064-29514233	K562	blood:	n/a	n/a
5	CEBPB	chr12:29518356-29518575	IMR90	lung:	n/a	n/a
6	CEBPB	chr12:29503062-29503325	MCF-7	breast:	n/a	n/a
7	CEBPB	chr12:29518360-29518606	K562	blood:	n/a	n/a
8	CEBPB	chr12:29503017-29503363	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr12:29506220-29506370	GM06990	blood:	n/a	n/a
10	CTCF	chr12:29518993-29519063	GM20000	blood:	n/a	n/a
11	CTCF	chr12:29513999-29514017	GM20000	blood:	n/a	n/a
12	CTCF	chr12:29510840-29510990	NB4	blood:	n/a	n/a
13	CTCF	chr12:29513986-29513991	GM20000	blood:	n/a	n/a
14	E2F4	chr12:29515669-29515713	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F4	chr12:29517208-29517270	MCF10A-Er-Src	breast:	n/a	n/a
16	E2F4	chr12:29507998-29508075	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr12:29503059-29503399	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr12:29503058-29503314	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr12:29503106-29503331	MCF10A-Er-Src	breast:	n/a	n/a
20	FOXA1	chr12:29503089-29503237	T-47D	breast:	n/a	n/a
21	FOXA1	chr12:29515875-29516094	A549	lung:	n/a	chr12:29515918-29515930
22	FOXA1	chr12:29502982-29503388	T-47D	breast:	n/a	n/a
23	GATA3	chr12:29502906-29503601	SK-N-SH	brain:	n/a	n/a
24	GATA3	chr12:29502857-29503684	SK-N-SH	brain:	n/a	n/a
25	IRF1	chr12:29505125-29505164	K562	blood:	n/a	n/a
26	JUN	chr12:29515968-29515986	H1-hESC	embryonic stem cell:	n/a	n/a
27	JUN	chr12:29503103-29503370	K562	blood:	n/a	n/a
28	JUN	chr12:29503188-29503349	H1-hESC	embryonic stem cell:	n/a	n/a
29	JUN	chr12:29520448-29520744	K562	blood:	n/a	n/a
30	KAP1	chr12:29521926-29522761	K562	blood:	n/a	n/a
31	KAP1	chr12:29522969-29523186	K562	blood:	n/a	n/a
32	MAFK	chr12:29510695-29510754	HepG2	liver:	n/a	chr12:29510731-29510747
33	MAFK	chr12:29514753-29514987	HepG2	liver:	n/a	n/a
34	MAZ	chr12:29511373-29511382	HepG2	liver:	n/a	n/a
35	NFIC	chr12:29502854-29503457	ECC-1	luminal epithelium:	n/a	n/a
36	NFIC	chr12:29502783-29503724	ECC-1	luminal epithelium:	n/a	n/a
37	NFIC	chr12:29502805-29503636	SK-N-SH	brain:	n/a	n/a
38	NFIC	chr12:29503062-29503448	SK-N-SH	brain:	n/a	n/a
39	NFYB	chr12:29511025-29511207	GM12878	blood:	n/a	n/a
40	POLR2A	chr12:29503053-29503383	SK-N-MC	brain:	n/a	n/a
41	POLR2A	chr12:29512918-29513050	GM12878	blood:	n/a	n/a
42	POLR2A	chr12:29512136-29512193	ProgFib	skin:	n/a	n/a
43	POLR2A	chr12:29509417-29509434	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr12:29521129-29521147	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr12:29520882-29520910	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr12:29517986-29518076	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr12:29504347-29504389	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr12:29518727-29518901	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr12:29504429-29504455	HUVEC	blood vessel:	n/a	n/a
50	POLR2A	chr12:29514775-29514852	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:29506350-29506400	GM12878	blood:	n/a
2	chr12:29506350-29506400	AG04450	lung:	fetal
3	chr12:29506350-29506400	BE2_C	brain:	n/a
4	chr12:29506350-29506400	HIPEpiC	eye:	n/a
5	chr12:29506350-29506400	H1-hESC	embryonic stem cell:	embryo
6	chr12:29506350-29506400	NH-A	brain:	n/a
7	chr12:29506350-29506400	SK-N-SH_RA	brain:	n/a
8	chr12:29506350-29506400	CMK	blood:	n/a
9	chr12:29506350-29506400	HL-60	blood:	n/a
10	chr12:29506350-29506400	SAEC	small airway:	n/a
11	chr12:29506350-29506400	HCM	heart:	n/a
12	chr12:29506350-29506400	AoSMC	blood vessel:	n/a
13	chr12:29506350-29506400	MCF-7	breast:	n/a
14	chr12:29506350-29506400	HepG2	liver:	n/a
15	chr12:29506350-29506400	HCPEpiC	choroid plexus:	n/a
16	chr12:29506350-29506400	GM12892	blood:	n/a
17	chr12:29506350-29506400	SK-N-SH	brain:	n/a
18	chr12:29506350-29506400	ProgFib	skin:	n/a
19	chr12:29506350-29506400	LNCaP	prostate:	n/a
20	chr12:29506350-29506400	MCF10A-Er-Src	breast:	n/a
21	chr12:29506350-29506400	NHBE	bronchial:	n/a
22	chr12:29506350-29506400	PFSK-1	brain:	n/a
23	chr12:29506350-29506400	NB4	blood:	n/a
24	chr12:29506350-29506400	HRE	kidney:	n/a
25	chr12:29506350-29506400	HNPCEpiC	eye:	n/a
26	chr12:29506350-29506400	BJ	skin:	n/a
27	chr12:29506350-29506400	HRPEpiC	eye:	n/a
28	chr12:29506350-29506400	GM19239	blood:	n/a
29	chr12:29506350-29506400	HPAEpiC	pulmonary alveolar:	n/a
30	chr12:29506350-29506400	GM06990	blood:	n/a
31	chr12:29506350-29506400	ovcar-3	ovarian:	n/a
32	chr12:29506350-29506400	SK-N-MC	brain:	n/a
33	chr12:29506350-29506400	ECC-1	luminal epithelium:	n/a
34	chr12:29506350-29506400	HEK293	kidney:	embryo
35	chr12:29506350-29506400	HCT-116	colon:	n/a
36	chr12:29506350-29506400	NT2-D1	testis:	n/a
37	chr12:29506350-29506400	U87	brain:	n/a
38	chr12:29506350-29506400	HUVEC	blood vessel:	n/a
39	chr12:29506350-29506400	GM12891	blood:	n/a
40	chr12:29506350-29506400	HAEpiC	amniotic membrane:	n/a
41	chr12:29506350-29506400	Hela-S3	cervix:	n/a
42	chr12:29506350-29506400	AG10803	skin:	n/a
43	chr12:29506350-29506400	AG04449	skin:	fetal
44	chr12:29506350-29506400	K562	blood:	n/a
45	chr12:29506350-29506400	Caco-2	colon:	n/a
46	chr12:29506350-29506400	T-47D	breast:	n/a
47	chr12:29506350-29506400	Jurkat	blood:	n/a
48	chr12:29506350-29506400	SKMC	muscle:	n/a
49	chr12:29506350-29506400	HCF	heart:	n/a
50	chr12:29506350-29506400	HEEpiC	esophagus:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:29501467..29504234-chr12:29504488..29507414,2	K562	blood:
2	chr12:29507582..29513596-chr12:29520320..29524566,6	K562	blood:
3	chr12:29520656..29526421-chr12:29532315..29535324,6	MCF-7	breast:
4	chr12:29514507..29517098-chr12:29519955..29522793,2	K562	blood:
5	chr12:29499488..29501163-chr12:29507438..29509843,2	K562	blood:
6	chr12:29504698..29507288-chr12:29512167..29514486,2	MCF-7	breast:
7	chr12:29523685..29526010-chr12:29528444..29531156,2	MCF-7	breast:
8	chr12:29502652..29504155-chr12:29507653..29509548,2	MCF-7	breast:
9	chr12:29516247..29519208-chr12:29526814..29530124,4	K562	blood:
10	chr12:29514732..29517650-chr12:29532470..29535161,2	MCF-7	breast:
11	chr12:29514507..29517098-chr12:29519955..29522793,2	K562	blood:
12	chr12:29501592..29504234-chr12:29504443..29507414,2	K562	blood:
13	chr12:29504698..29507288-chr12:29512167..29514486,2	MCF-7	breast:
14	chr12:29503193..29506083-chr12:30783016..30785826,2	MCF-7	breast:
15	chr12:29489097..29490633-chr12:29512483..29514735,2	K562	blood:
16	chr12:29519283..29521752-chr12:29527827..29530513,2	K562	blood:
17	chr12:29505820..29507977-chr12:29508931..29512275,3	K562	blood:
18	chr12:29301582..29303959-chr12:29510766..29513729,2	K562	blood:

No data

Variant related genes	Relation type
ERGIC2	TF binding region
ERGIC2	CpG island
ENSG00000087502	chromatin interactions
ENSG00000064763	chromatin interactions
ENSG00000257258	chromatin interactions

Extended variants
information (count: 699 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:699 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3764952	chr12:29501941-29501942	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369200675	chr12:29501946-29501947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200840441	chr12:29502011-29502012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200158590	chr12:29502012-29502013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533307798	chr12:29502018-29502019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538458758	chr12:29502050-29502051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs199688319	chr12:29502059-29502060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376952708	chr12:29502113-29502114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370711662	chr12:29502135-29502136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528732899	chr12:29502225-29502226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs3764953	chr12:29502236-29502237	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs114575020	chr12:29502274-29502275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534270256	chr12:29502275-29502276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555826158	chr12:29502287-29502288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563969685	chr12:29502298-29502299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571873568	chr12:29502356-29502357	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574104022	chr12:29502385-29502386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183421674	chr12:29502435-29502436	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185855232	chr12:29502471-29502472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191991292	chr12:29502485-29502486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369325553	chr12:29502545-29502546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549846057	chr12:29502563-29502564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545322006	chr12:29502602-29502603	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565487018	chr12:29502658-29502659	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545615128	chr12:29502668-29502669	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs141169455	chr12:29502785-29502786	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs34762815	chr12:29502829-29502830	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs12580072	chr12:29502852-29502853	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs560615928	chr12:29502905-29502906	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs373369156	chr12:29502923-29502924	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372031276	chr12:29502927-29502928	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs376348079	chr12:29502937-29502938	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531219614	chr12:29502994-29502995	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549322300	chr12:29503008-29503009	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs374870823	chr12:29503017-29503018	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs565082336	chr12:29503024-29503025	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs139010014	chr12:29503027-29503028	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs547309543	chr12:29503052-29503053	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs182909183	chr12:29503069-29503070	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs529884139	chr12:29503106-29503107	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs549511163	chr12:29503113-29503114	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs567720959	chr12:29503152-29503153	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs35962253	chr12:29503215-29503216	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs188115776	chr12:29503274-29503275	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs192744342	chr12:29503299-29503300	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs374978512	chr12:29503308-29503309	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs554142775	chr12:29503310-29503311	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs143775713	chr12:29503367-29503368	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs542772387	chr12:29503379-29503380	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs113773206	chr12:29503383-29503384	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Acute myeloid leukemia	20729466	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:566 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29427200-29527400	Weak transcription	Small Intestine	intestine
2	chr12:29462600-29533000	Weak transcription	Aorta	Aorta
3	chr12:29470800-29508400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr12:29470800-29532800	Weak transcription	Right Ventricle	heart
5	chr12:29473800-29522600	Weak transcription	NHEK	skin
6	chr12:29476000-29502600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr12:29476200-29509400	Weak transcription	Spleen	Spleen
8	chr12:29476200-29512800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr12:29476200-29533400	Weak transcription	Pancreas	Pancrea
10	chr12:29476400-29509600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr12:29476400-29532600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr12:29476400-29533200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr12:29477000-29517800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr12:29483400-29518000	Weak transcription	Brain Hippocampus Middle	brain
15	chr12:29484200-29532000	Weak transcription	Fetal Brain Male	brain
16	chr12:29485600-29533400	Weak transcription	Gastric	stomach
17	chr12:29486800-29528600	Weak transcription	Psoas Muscle	Psoas
18	chr12:29487000-29533000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr12:29488600-29503800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr12:29488800-29532000	Weak transcription	NHLF	lung
21	chr12:29489600-29525600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr12:29489800-29510000	Weak transcription	Brain Germinal Matrix	brain
23	chr12:29490000-29502800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr12:29490000-29533400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:29490000-29533400	Weak transcription	Esophagus	oesophagus
26	chr12:29490200-29502000	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr12:29490200-29502200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:29490200-29506000	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr12:29490400-29502800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr12:29490400-29524600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr12:29490600-29502000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr12:29490600-29503000	Strong transcription	Primary monocytes fromperipheralblood	blood
33	chr12:29491000-29511400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr12:29491200-29502600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr12:29491400-29506400	Strong transcription	Primary T helper cells PMA-I stimulated	--
36	chr12:29492200-29502800	Strong transcription	Placenta	Placenta
37	chr12:29492400-29502000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
38	chr12:29492400-29511800	Strong transcription	HUES64 Cell Line	embryonic stem cell
39	chr12:29492400-29518000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr12:29492800-29511800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr12:29492800-29519000	Weak transcription	HepG2	liver
42	chr12:29493000-29503200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr12:29493200-29504800	Strong transcription	Primary T helper cells fromperipheralblood	blood
44	chr12:29493600-29532600	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr12:29494400-29517800	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr12:29494400-29532400	Weak transcription	Brain Substantia Nigra	brain
47	chr12:29494600-29509000	Weak transcription	Lung	lung
48	chr12:29494600-29511800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr12:29494600-29532800	Weak transcription	Colonic Mucosa	Colon
50	chr12:29495800-29503400	Strong transcription	HUES6 Cell Line	embryonic stem cell

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