Variant report

Variant	nsv534344
Chromosome Location	chr3:75028665-75164716
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:324)
CpG islands
(count:245)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75050631-75050697	HepG2	liver:	n/a	n/a
2	ATF2	chr3:75150761-75151146	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr3:75150556-75150840	GM12878	blood:	n/a	n/a
4	CEBPB	chr3:75050542-75050920	H1-hESC	embryonic stem cell:	n/a	chr3:75050640-75050653
5	CEBPB	chr3:75094866-75095145	IMR90	lung:	n/a	chr3:75095016-75095029 chr3:75095016-75095029 chr3:75095016-75095027 chr3:75095016-75095029 chr3:75095018-75095029
6	CEBPB	chr3:75029160-75029513	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr3:75087558-75087752	IMR90	lung:	n/a	n/a
8	CEBPB	chr3:75079121-75079287	A549	lung:	n/a	n/a
9	CEBPB	chr3:75097578-75097711	A549	lung:	n/a	n/a
10	CEBPB	chr3:75102589-75102881	HepG2	liver:	n/a	chr3:75102718-75102729
11	CEBPB	chr3:75094960-75095164	HepG2	liver:	n/a	chr3:75095016-75095029 chr3:75095016-75095029 chr3:75095016-75095027 chr3:75095016-75095029 chr3:75095018-75095029
12	CEBPB	chr3:75050603-75050853	HepG2	liver:	n/a	chr3:75050640-75050653
13	CEBPB	chr3:75149260-75149266	A549	lung:	n/a	n/a
14	CEBPB	chr3:75068263-75068486	HepG2	liver:	n/a	chr3:75068399-75068412 chr3:75068399-75068410 chr3:75068399-75068412 chr3:75068288-75068299 chr3:75068401-75068412
15	CEBPB	chr3:75152232-75152515	HepG2	liver:	n/a	chr3:75152367-75152378
16	CHD2	chr3:75150518-75151233	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTBP2	chr3:75150599-75151276	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr3:75050600-75050750	AG09309	skin:	n/a	n/a
19	CTCF	chr3:75050558-75050734	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr3:75050620-75050770	NB4	blood:	n/a	n/a
21	CTCF	chr3:75092140-75092290	HepG2	liver:	n/a	n/a
22	CTCF	chr3:75050620-75050770	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chr3:75050640-75050790	BE2_C	brain:	n/a	n/a
24	CTCF	chr3:75050660-75050810	AG09309	skin:	n/a	n/a
25	CTCF	chr3:75032021-75032096	GM20000	blood:	n/a	n/a
26	CTCF	chr3:75092135-75092294	T-47D	breast:	n/a	n/a
27	CTCF	chr3:75050600-75050750	AG04450	lung:	n/a	n/a
28	CTCF	chr3:75092160-75092310	SAEC	small airway:	n/a	n/a
29	CTCF	chr3:75050580-75050730	HEEpiC	esophagus:	n/a	n/a
30	CTCF	chr3:75050620-75050770	MCF-7	breast:	n/a	n/a
31	CTCF	chr3:75050600-75050750	HepG2	liver:	n/a	n/a
32	CTCF	chr3:75050660-75050768	GM10248	blood:	n/a	n/a
33	CTCF	chr3:75091080-75091230	HRE	kidney:	n/a	n/a
34	CTCF	chr3:75050647-75050758	GM13977	blood:	n/a	n/a
35	CTCF	chr3:75050620-75050770	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr3:75057173-75057287	GM10248	blood:	n/a	n/a
37	CTCF	chr3:75088497-75088520	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr3:75050526-75050869	IMR90	lung:	n/a	n/a
39	CTCF	chr3:75050660-75050810	HCM	heart:	n/a	n/a
40	CTCF	chr3:75050571-75050821	LNCaP	prostate:	n/a	n/a
41	CTCF	chr3:75050600-75050750	AG04449	skin:	n/a	n/a
42	CTCF	chr3:75050660-75050810	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr3:75050620-75050770	HEK293	kidney:	n/a	n/a
44	CTCF	chr3:75050600-75050750	HRE	kidney:	n/a	n/a
45	CTCF	chr3:75052284-75052360	GM13976	blood:	n/a	n/a
46	CTCF	chr3:75050493-75050842	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:75050620-75050770	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr3:75157317-75157361	LNCaP	prostate:	n/a	n/a
49	CTCF	chr3:75092200-75092350	HMEC	breast:	n/a	n/a
50	CTCF	chr3:75050656-75050782	MCF-7	breast:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75028964-75029014	GM12878	blood:	n/a
2	chr3:75028964-75029014	GM12878	blood:	n/a
3	chr3:75033413-75033463	HAEpiC	amniotic membrane:	n/a
4	chr3:75150999-75151049	HCF	heart:	n/a
5	chr3:75033413-75033463	Hepatocyte	liver:	n/a
6	chr3:75150999-75151049	Hepatocyte	liver:	n/a
7	chr3:75033413-75033463	HCM	heart:	n/a
8	chr3:75033413-75033463	IMR90	lung:	fetal
9	chr3:75150999-75151049	H1-hESC	embryonic stem cell:	embryo
10	chr3:75146913-75146963	SK-N-SH	brain:	n/a
11	chr3:75028964-75029014	AG09309	skin:	n/a
12	chr3:75033413-75033463	GM06990	blood:	n/a
13	chr3:75033413-75033463	HRCEpiC	kidney:	n/a
14	chr3:75028964-75029014	PFSK-1	brain:	n/a
15	chr3:75150999-75151049	MCF10A-Er-Src	breast:	n/a
16	chr3:75028964-75029014	NHBE	bronchial:	n/a
17	chr3:75150999-75151049	GM12892	blood:	n/a
18	chr3:75028964-75029014	HEEpiC	esophagus:	n/a
19	chr3:75033413-75033463	NH-A	brain:	n/a
20	chr3:75033413-75033463	AG09309	skin:	n/a
21	chr3:75146913-75146963	AG04450	lung:	fetal
22	chr3:75033413-75033463	GM12891	blood:	n/a
23	chr3:75146913-75146963	ECC-1	luminal epithelium:	n/a
24	chr3:75033413-75033463	GM19239	blood:	n/a
25	chr3:75150999-75151049	A549	lung:	n/a
26	chr3:75033413-75033463	SKMC	muscle:	n/a
27	chr3:75033413-75033463	K562	blood:	n/a
28	chr3:75146913-75146963	LNCaP	prostate:	n/a
29	chr3:75150999-75151049	BJ	skin:	n/a
30	chr3:75146913-75146963	HIPEpiC	eye:	n/a
31	chr3:75146913-75146963	GM12891	blood:	n/a
32	chr3:75150999-75151049	T-47D	breast:	n/a
33	chr3:75028964-75029014	HUVEC	blood vessel:	n/a
34	chr3:75028964-75029014	NH-A	brain:	n/a
35	chr3:75033413-75033463	SK-N-MC	brain:	n/a
36	chr3:75028964-75029014	Caco-2	colon:	n/a
37	chr3:75150999-75151049	BE2_C	brain:	n/a
38	chr3:75028964-75029014	PrEC	prostate:	n/a
39	chr3:75146913-75146963	NT2-D1	testis:	n/a
40	chr3:75033413-75033463	SK-N-SH	brain:	n/a
41	chr3:75028964-75029014	T-47D	breast:	n/a
42	chr3:75028964-75029014	CMK	blood:	n/a
43	chr3:75146913-75146963	BE2_C	brain:	n/a
44	chr3:75033413-75033463	HNPCEpiC	eye:	n/a
45	chr3:75028964-75029014	A549	lung:	n/a
46	chr3:75150999-75151049	AG04450	lung:	fetal
47	chr3:75146913-75146963	GM19239	blood:	n/a
48	chr3:75150999-75151049	HUVEC	blood vessel:	n/a
49	chr3:75033413-75033463	T-47D	breast:	n/a
50	chr3:75146913-75146963	HepG2	liver:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:74316601..74317358-chr3:75050152..75051148,4	MCF-7	breast:
2	chr3:75126105..75128308-chr3:75131870..75133560,2	MCF-7	breast:
3	chr17:59890049..59891797-chr3:75078865..75080866,2	MCF-7	breast:
4	chr3:75105526..75106181-chr3:75220559..75221295,2	MCF-7	breast:
5	chr3:74116070..74116803-chr3:75050321..75051115,3	MCF-7	breast:
6	chr3:73917560..73918578-chr3:75050342..75051099,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-13	chr3:75133306-75134388	NONHSAT090497

No data

Variant related genes	Relation type
NIPA2P2	TF binding region
NIPA2P2	CpG island
ENSG00000113805	chromatin interactions
ENSG00000241022	chromatin interactions

Extended variants
information (count: 1875 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1875 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372491400	chr3:75028794-75028795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191062933	chr3:75028855-75028856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547786959	chr3:75028904-75028905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551800291	chr3:75028963-75028964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183959064	chr3:75028965-75028966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528003151	chr3:75029013-75029014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559347165	chr3:75029081-75029082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs578160484	chr3:75029085-75029086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561344643	chr3:75029116-75029117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150709387	chr3:75029159-75029160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs62266824	chr3:75029161-75029162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187708661	chr3:75029187-75029188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375230526	chr3:75029257-75029258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76712473	chr3:75029265-75029266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538582316	chr3:75029346-75029347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553374451	chr3:75029348-75029349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs111326691	chr3:75029382-75029383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536168773	chr3:75029398-75029399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs137926504	chr3:75029417-75029418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs576226450	chr3:75029534-75029535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557158786	chr3:75029559-75029560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529913139	chr3:75029581-75029582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs200064547	chr3:75029582-75029583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192582754	chr3:75029724-75029725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78312252	chr3:75029744-75029745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs578048422	chr3:75029763-75029764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542760297	chr3:75029774-75029775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114778028	chr3:75029846-75029847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146148820	chr3:75029854-75029855	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112796329	chr3:75029855-75029856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183090149	chr3:75029880-75029881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140203842	chr3:75029919-75029920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550112160	chr3:75029957-75029958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567208837	chr3:75029963-75029964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369170140	chr3:75030005-75030006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573199447	chr3:75030031-75030032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532092633	chr3:75030133-75030134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs114295829	chr3:75030302-75030303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564430544	chr3:75030341-75030342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529705442	chr3:75030350-75030351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143797185	chr3:75030378-75030379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144788265	chr3:75030386-75030387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537220285	chr3:75030420-75030421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558485797	chr3:75030428-75030429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550085941	chr3:75030464-75030465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186991479	chr3:75030480-75030481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554207713	chr3:75030546-75030547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148523608	chr3:75030547-75030548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543054218	chr3:75030578-75030579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561583674	chr3:75030585-75030586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75028400-75030000	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr3:75028600-75029000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr3:75028600-75029200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
4	chr3:75028600-75029800	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr3:75028600-75029800	Enhancers	H1 Cell Line	embryonic stem cell
6	chr3:75028600-75029800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr3:75028600-75030000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr3:75028600-75030400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr3:75028600-75030600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr3:75028800-75029000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr3:75028800-75029800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr3:75029000-75029200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr3:75029200-75029600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr3:75029600-75029800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr3:75029600-75030600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr3:75029600-75035600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr3:75030400-75035400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr3:75030600-75035000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr3:75035000-75035800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr3:75035000-75036000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr3:75035200-75036000	Enhancers	H1 Cell Line	embryonic stem cell
22	chr3:75035400-75035800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr3:75035400-75036000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr3:75035600-75035800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr3:75040400-75041200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr3:75060600-75060800	Enhancers	Fetal Brain Male	brain
27	chr3:75060800-75061600	Weak transcription	Fetal Brain Male	brain
28	chr3:75061000-75063600	Enhancers	Brain Germinal Matrix	brain
29	chr3:75061200-75063000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr3:75061400-75064000	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr3:75061600-75061800	Enhancers	Fetal Brain Male	brain
32	chr3:75061600-75062800	Enhancers	Fetal Heart	heart
33	chr3:75061600-75063400	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr3:75061800-75063200	Weak transcription	Fetal Brain Male	brain
35	chr3:75061800-75064200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr3:75062000-75062800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr3:75063200-75063600	Enhancers	Fetal Brain Male	brain
38	chr3:75063600-75065400	Weak transcription	Fetal Brain Male	brain
39	chr3:75064000-75067000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr3:75065400-75065600	Enhancers	Fetal Brain Male	brain
41	chr3:75067000-75067200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr3:75067200-75067600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr3:75067600-75069600	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr3:75068600-75068800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr3:75070400-75071000	Enhancers	Rectal Smooth Muscle	rectum
46	chr3:75076800-75077200	Enhancers	Fetal Intestine Large	intestine
47	chr3:75077200-75078200	Weak transcription	Fetal Intestine Large	intestine
48	chr3:75078200-75080600	Enhancers	Fetal Intestine Large	intestine
49	chr3:75078400-75081200	Enhancers	Fetal Intestine Small	intestine
50	chr3:75078800-75079800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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