Variant report

Variant	esv3409612
Chromosome Location	chr4:1230802-1233300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:108)
CpG islands
(count:369)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:108 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:1232822-1233094	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr4:1232792-1233103	A549	lung:	n/a	n/a
3	CEBPB	chr4:1232791-1233022	K562	blood:	n/a	n/a
4	CEBPB	chr4:1232796-1233114	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr4:1232781-1233126	K562	blood:	n/a	n/a
6	CEBPB	chr4:1232773-1233171	MCF-7	breast:	n/a	n/a
7	CEBPB	chr4:1232778-1233107	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:1232801-1233122	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:1232739-1233066	A549	lung:	n/a	n/a
10	CTCF	chr4:1230720-1230870	WERI-Rb-1	eye:	n/a	n/a
11	CTCF	chr4:1233080-1233230	HRPEpiC	eye:	n/a	n/a
12	EP300	chr4:1231360-1231584	GM12878	blood:	n/a	n/a
13	ESR1	chr4:1232974-1233459	ECC-1	luminal epithelium:	n/a	chr4:1233224-1233241
14	ESR1	chr4:1232973-1233397	ECC-1	luminal epithelium:	n/a	chr4:1233224-1233241
15	ESR1	chr4:1232956-1233423	ECC-1	luminal epithelium:	n/a	chr4:1233224-1233241
16	ESR1	chr4:1233117-1233419	ECC-1	luminal epithelium:	n/a	chr4:1233224-1233241
17	FOS	chr4:1232858-1232986	MCF10A-Er-Src	breast:	n/a	n/a
18	FOSL2	chr4:1231280-1231636	HepG2	liver:	n/a	n/a
19	HEY1	chr4:1231282-1231609	HepG2	liver:	n/a	n/a
20	NR3C1	chr4:1230278-1230883	A549	lung:	n/a	n/a
21	PBX3	chr4:1231358-1231489	GM12878	blood:	n/a	n/a
22	POLR2A	chr4:1231099-1231798	GM12891	blood:	n/a	n/a
23	POLR2A	chr4:1231969-1231972	K562	blood:	n/a	n/a
24	POLR2A	chr4:1232911-1235081	GM12878	blood:	n/a	n/a
25	POLR2A	chr4:1230809-1231360	K562	blood:	n/a	n/a
26	POLR2A	chr4:1231138-1231499	K562	blood:	n/a	n/a
27	POLR2A	chr4:1232958-1233762	GM12878	blood:	n/a	n/a
28	POLR2A	chr4:1233225-1233231	K562	blood:	n/a	n/a
29	POLR2A	chr4:1231984-1232134	K562	blood:	n/a	n/a
30	POLR2A	chr4:1230220-1232117	GM12891	blood:	n/a	n/a
31	POLR2A	chr4:1230117-1232164	GM12891	blood:	n/a	n/a
32	POLR2A	chr4:1230046-1232219	GM12892	blood:	n/a	n/a
33	POLR2A	chr4:1231279-1231585	A549	lung:	n/a	n/a
34	POLR2A	chr4:1233073-1233131	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr4:1231558-1234052	K562	blood:	n/a	n/a
36	POLR2A	chr4:1232253-1232327	K562	blood:	n/a	n/a
37	POLR2A	chr4:1231410-1231793	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr4:1232732-1232742	K562	blood:	n/a	n/a
39	POLR2A	chr4:1230865-1231831	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr4:1230850-1231108	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr4:1232749-1232789	K562	blood:	n/a	n/a
42	POLR2A	chr4:1231593-1232174	HL-60	blood:	n/a	n/a
43	POLR2A	chr4:1231908-1232073	K562	blood:	n/a	n/a
44	POLR2A	chr4:1230161-1231979	GM12892	blood:	n/a	n/a
45	POLR2A	chr4:1230692-1230967	K562	blood:	n/a	n/a
46	POLR2A	chr4:1231881-1231917	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr4:1231734-1231963	A549	lung:	n/a	n/a
48	POLR2A	chr4:1231317-1231764	A549	lung:	n/a	n/a
49	POLR2A	chr4:1231756-1232088	HepG2	liver:	n/a	n/a
50	POLR2A	chr4:1232572-1232648	K562	blood:	n/a	n/a

(count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1232112-1232162	ProgFib	skin:	n/a
2	chr4:1232787-1232837	HPAEpiC	pulmonary alveolar:	n/a
3	chr4:1232112-1232162	SAEC	small airway:	n/a
4	chr4:1232112-1232162	ProgFib	skin:	n/a
5	chr4:1232787-1232837	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:1232112-1232162	SAEC	small airway:	n/a
7	chr4:1232000-1232050	HRE	kidney:	n/a
8	chr4:1231840-1231890	NT2-D1	testis:	n/a
9	chr4:1232112-1232162	SK-N-SH	brain:	n/a
10	chr4:1232739-1232789	SK-N-SH_RA	brain:	n/a
11	chr4:1232787-1232837	HCT-116	colon:	n/a
12	chr4:1232112-1232162	HEEpiC	esophagus:	n/a
13	chr4:1232787-1232837	GM12878	blood:	n/a
14	chr4:1232739-1232789	AG04450	lung:	fetal
15	chr4:1232787-1232837	Caco-2	colon:	n/a
16	chr4:1232112-1232162	SK-N-SH_RA	brain:	n/a
17	chr4:1232787-1232837	HCF	heart:	n/a
18	chr4:1231840-1231890	SK-N-SH	brain:	n/a
19	chr4:1232112-1232162	SK-N-MC	brain:	n/a
20	chr4:1232170-1232220	HCM	heart:	n/a
21	chr4:1232170-1232220	HEK293	kidney:	embryo
22	chr4:1232112-1232162	HRE	kidney:	n/a
23	chr4:1232787-1232837	HRPEpiC	eye:	n/a
24	chr4:1232787-1232837	AG09319	gingival:	n/a
25	chr4:1231840-1231890	HEK293	kidney:	embryo
26	chr4:1232787-1232837	BE2_C	brain:	n/a
27	chr4:1232112-1232162	HEK293	kidney:	embryo
28	chr4:1232000-1232050	NHBE	bronchial:	n/a
29	chr4:1232739-1232789	T-47D	breast:	n/a
30	chr4:1232787-1232837	HEEpiC	esophagus:	n/a
31	chr4:1232170-1232220	U87	brain:	n/a
32	chr4:1231840-1231890	NHDF-neo	bronchial:	n/a
33	chr4:1232000-1232050	ECC-1	luminal epithelium:	n/a
34	chr4:1232170-1232220	K562	blood:	n/a
35	chr4:1232112-1232162	PANC-1	pancreas:	n/a
36	chr4:1232000-1232050	NH-A	brain:	n/a
37	chr4:1232000-1232050	AG10803	skin:	n/a
38	chr4:1232787-1232837	PrEC	prostate:	n/a
39	chr4:1232000-1232050	HRPEpiC	eye:	n/a
40	chr4:1232739-1232789	SAEC	small airway:	n/a
41	chr4:1232787-1232837	NH-A	brain:	n/a
42	chr4:1232787-1232837	HEK293	kidney:	embryo
43	chr4:1231840-1231890	Hepatocyte	liver:	n/a
44	chr4:1232112-1232162	GM19239	blood:	n/a
45	chr4:1232170-1232220	ECC-1	luminal epithelium:	n/a
46	chr4:1232787-1232837	HCM	heart:	n/a
47	chr4:1232000-1232050	Caco-2	colon:	n/a
48	chr4:1232112-1232162	HCM	heart:	n/a
49	chr4:1232739-1232789	HRE	kidney:	n/a
50	chr4:1231840-1231890	GM12878	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1233077..1236112-chr4:1282661..1284848,3	MCF-7	breast:
2	chr4:1232098..1233809-chr4:1299016..1301525,2	K562	blood:
3	chr4:1227874..1230921-chr4:1231910..1234082,4	MCF-7	breast:
4	chr4:976786..978609-chr4:1230405..1232762,2	K562	blood:
5	chr4:1231578..1233749-chr4:1664343..1666547,2	K562	blood:
6	chr4:1144843..1147526-chr4:1230222..1232389,2	MCF-7	breast:
7	chr4:1227874..1230921-chr4:1231910..1234082,4	MCF-7	breast:
8	chr4:1230672..1232310-chr4:1283727..1285762,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CTBP1	hsa-miR-10b-5p	chr4:1231354-1231376

Variant related genes	Relation type
CTBP1	TF binding region
CTBP1	CpG island
ENSG00000215367	chromatin interactions
ENSG00000227189	chromatin interactions
ENSG00000090316	chromatin interactions

Extended variants
information (count: 163 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:163 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575690900	chr4:1230811-1230812	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs542756153	chr4:1230830-1230831	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs560933519	chr4:1230869-1230870	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs576604389	chr4:1230877-1230878	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs118115252	chr4:1230883-1230884	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs116513771	chr4:1230902-1230903	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs369599332	chr4:1230938-1230939	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs577959669	chr4:1230947-1230948	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs79897798	chr4:1230959-1230960	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs76602977	chr4:1230960-1230961	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs532306540	chr4:1230983-1230984	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs550745655	chr4:1231007-1231008	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs562579752	chr4:1231023-1231024	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs529799021	chr4:1231036-1231037	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs548332282	chr4:1231037-1231038	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs531498684	chr4:1231058-1231059	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs141983754	chr4:1231059-1231060	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs533734284	chr4:1231084-1231085	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs551897203	chr4:1231112-1231113	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs571864037	chr4:1231121-1231122	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs367585132	chr4:1231150-1231151	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs371341013	chr4:1231157-1231158	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs557524079	chr4:1231183-1231184	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs112296638	chr4:1231209-1231210	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs575470194	chr4:1231219-1231220	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs113981130	chr4:1231238-1231239	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs112203392	chr4:1231245-1231246	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs369135878	chr4:1231259-1231260	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs200291490	chr4:1231312-1231313	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs554617340	chr4:1231324-1231325	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs76762203	chr4:1231359-1231360	Weak transcription Strong transcription	TF binding region Chromatin interactive region miRNA target site	3 gene(s)	Overlapped CNVs	n/a
32	rs540572015	chr4:1231366-1231367	Weak transcription Strong transcription	TF binding region Chromatin interactive region miRNA target site	3 gene(s)	Overlapped CNVs	n/a
33	rs111585941	chr4:1231378-1231379	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs111709671	chr4:1231385-1231386	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs558725490	chr4:1231407-1231408	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs577055279	chr4:1231426-1231427	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs544213561	chr4:1231427-1231428	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs562680196	chr4:1231428-1231429	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs151114452	chr4:1231435-1231436	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
40	rs372900971	chr4:1231466-1231467	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs376112446	chr4:1231470-1231471	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs113461383	chr4:1231486-1231487	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs529885937	chr4:1231498-1231499	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs112048066	chr4:1231505-1231506	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs370857343	chr4:1231521-1231522	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs185297901	chr4:1231534-1231535	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs560250263	chr4:1231547-1231548	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs527386773	chr4:1231556-1231557	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs552147686	chr4:1231570-1231571	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs570394785	chr4:1231576-1231577	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20393555	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1204400-1235800	Strong transcription	HUES6 Cell Line	embryonic stem cell
2	chr4:1204600-1236200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:1204800-1237000	Weak transcription	Psoas Muscle	Psoas
4	chr4:1211400-1235400	Weak transcription	Small Intestine	intestine
5	chr4:1211600-1235400	Strong transcription	Sigmoid Colon	Sigmoid Colon
6	chr4:1212600-1237000	Strong transcription	Dnd41	blood
7	chr4:1214200-1235600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr4:1214200-1236800	Strong transcription	Primary T cells from cord blood	blood
9	chr4:1214400-1235200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr4:1214400-1235600	Strong transcription	H1 Cell Line	embryonic stem cell
11	chr4:1214400-1236400	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr4:1214400-1238400	Strong transcription	Thymus	Thymus
13	chr4:1214600-1235800	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr4:1214600-1236200	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr4:1215000-1235200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr4:1215000-1236000	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr4:1215400-1236000	Strong transcription	Primary B cells from peripheral blood	blood
18	chr4:1215800-1235600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr4:1216400-1235400	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chr4:1216400-1236000	Strong transcription	Fetal Thymus	thymus
21	chr4:1216600-1236000	Strong transcription	GM12878-XiMat	blood
22	chr4:1217200-1235400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
23	chr4:1217200-1235800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
24	chr4:1217600-1235200	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr4:1218200-1234600	Strong transcription	Primary T cells fromperipheralblood	blood
26	chr4:1218800-1235400	Strong transcription	H9 Cell Line	embryonic stem cell
27	chr4:1219000-1235400	Strong transcription	Gastric	stomach
28	chr4:1219000-1240200	Weak transcription	Hela-S3	cervix
29	chr4:1219800-1234800	Strong transcription	Fetal Intestine Large	intestine
30	chr4:1220600-1235400	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr4:1221600-1236400	Weak transcription	Fetal Heart	heart
32	chr4:1221600-1240200	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr4:1221800-1236400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr4:1222000-1240800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr4:1222600-1236000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr4:1223000-1236600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr4:1223200-1236800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
38	chr4:1223600-1234200	Strong transcription	Osteobl	bone
39	chr4:1223600-1234800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr4:1223800-1236200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:1224000-1235400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
42	chr4:1225000-1240200	Weak transcription	K562	blood
43	chr4:1226800-1232200	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr4:1226800-1235000	Strong transcription	Brain Substantia Nigra	brain
45	chr4:1227000-1235200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
46	chr4:1227200-1235200	Strong transcription	HepG2	liver
47	chr4:1227600-1234800	Strong transcription	Colonic Mucosa	Colon
48	chr4:1227600-1235800	Strong transcription	Placenta Amnion	Placenta Amnion
49	chr4:1227800-1236600	Strong transcription	Fetal Brain Female	brain
50	chr4:1228000-1231000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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