Variant report

Variant	nsv1043383
Chromosome Location	chr9:73517062-73556679
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	chr9:73540004-73540193	K562	blood:	n/a	n/a
2	BACH1	chr9:73536143-73536470	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr9:73549591-73549940	H1-hESC	embryonic stem cell:	n/a	chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549758-73549769
4	CEBPB	chr9:73549560-73549906	ECC-1	luminal epithelium:	n/a	chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549758-73549769
5	CEBPB	chr9:73517569-73518184	IMR90	lung:	n/a	n/a
6	CEBPB	chr9:73549583-73549920	K562	blood:	n/a	chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549758-73549769
7	CEBPB	chr9:73549584-73549929	HepG2	liver:	n/a	chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549758-73549769
8	CEBPB	chr9:73549575-73549939	IMR90	lung:	n/a	chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549758-73549769
9	CEBPB	chr9:73550979-73551192	IMR90	lung:	n/a	chr9:73551074-73551087 chr9:73551074-73551087
10	CEBPB	chr9:73539039-73540243	IMR90	lung:	n/a	chr9:73539926-73539939
11	CEBPB	chr9:73549589-73549950	A549	lung:	n/a	chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549760-73549769 chr9:73549758-73549769
12	CEBPB	chr9:73517649-73517924	Hela-S3	cervix:	n/a	n/a
13	CHD1	chr9:73527729-73527752	GM12878	blood:	n/a	n/a
14	CTCF	chr9:73539903-73540196	GM12878	blood:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
15	CTCF	chr9:73539844-73540171	T-47D	breast:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
16	CTCF	chr9:73540000-73540150	GM12801	blood:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
17	CTCF	chr9:73540020-73540170	K562	blood:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
18	CTCF	chr9:73539980-73540130	AG09309	skin:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
19	CTCF	chr9:73539960-73540110	WERI-Rb-1	eye:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
20	CTCF	chr9:73539895-73540201	HUVEC	blood vessel:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
21	CTCF	chr9:73539980-73540130	HRPEpiC	eye:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
22	CTCF	chr9:73539891-73540146	A549	lung:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
23	CTCF	chr9:73539960-73540110	GM12875	blood:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
24	CTCF	chr9:73539920-73540070	HFF	foreskin:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
25	CTCF	chr9:73539885-73540154	ProgFib	skin:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
26	CTCF	chr9:73539940-73540090	HRE	kidney:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
27	CTCF	chr9:73539940-73540090	GM12867	blood:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
28	CTCF	chr9:73539980-73540130	NHDF-neo	bronchial:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
29	CTCF	chr9:73539980-73540130	HMF	breast:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
30	CTCF	chr9:73539954-73540082	GM19240	blood:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
31	CTCF	chr9:73539980-73540130	NHLF	lung:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
32	CTCF	chr9:73539926-73540160	Kidney_OC	kidney:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
33	CTCF	chr9:73539835-73540251	K562	blood:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
34	CTCF	chr9:73539940-73540090	HEK293	kidney:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
35	CTCF	chr9:73539980-73540130	Caco-2	colon:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
36	CTCF	chr9:73539964-73540132	GM20000	blood:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
37	CTCF	chr9:73539910-73540190	Spleen_OC	spleen:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
38	CTCF	chr9:73539961-73540146	Lung_OC	lung:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
39	CTCF	chr9:73539554-73540452	A549	lung:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
40	CTCF	chr9:73539940-73540090	MCF-7	breast:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
41	CTCF	chr9:73539853-73540175	ECC-1	luminal epithelium:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
42	CTCF	chr9:73539860-73540213	ECC-1	luminal epithelium:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
43	CTCF	chr9:73539960-73540110	GM12871	blood:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
44	CTCF	chr9:73540020-73540170	HFF-Myc	foreskin:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
45	CTCF	chr9:73539940-73540090	GM12872	blood:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
46	CTCF	chr9:73539940-73540090	GM12875	blood:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
47	CTCF	chr9:73539920-73540070	HUVEC	blood vessel:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
48	CTCF	chr9:73539960-73540110	HCPEpiC	choroid plexus:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
49	CTCF	chr9:73539940-73540090	GM12866	blood:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060
50	CTCF	chr9:73539960-73540110	BE2_C	brain:	n/a	chr9:73540045-73540061 chr9:73540044-73540062 chr9:73540046-73540067 chr9:73540047-73540060

No.	Distal block	Cell Line	Cell type
1	chr9:73539136..73540497-chr9:73616477..73617366,8	MCF-7	breast:
2	chr9:73539689..73540473-chr9:73864229..73864817,3	MCF-7	breast:
3	chr9:73542298..73544919-chr9:73545647..73547854,2	MCF-7	breast:
4	chr9:73539587..73540524-chr9:73864401..73865325,3	K562	blood:
5	chr9:73542298..73544919-chr9:73545647..73547854,2	MCF-7	breast:
6	chr9:73539566..73540528-chr9:73864349..73865391,8	MCF-7	breast:
7	chr9:73541049..73541656-chr9:73864349..73864905,2	K562	blood:
8	chr9:73254988..73255819-chr9:73539510..73540543,3	MCF-7	breast:
9	chr9:73539789..73540480-chr9:73863378..73863879,2	MCF-7	breast:

Variant related genes	Relation type
PIGUP1	TF binding region

Extended variants
information (count: 1521 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1521 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4143736	chr9:73517105-73517106	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539420856	chr9:73517132-73517133	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs182209831	chr9:73517163-73517164	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs571129882	chr9:73517173-73517174	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs546434097	chr9:73517183-73517184	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs535231670	chr9:73517191-73517192	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs553248396	chr9:73517192-73517193	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs116262209	chr9:73517274-73517275	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs77799565	chr9:73517290-73517291	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs557405149	chr9:73517329-73517330	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs575267623	chr9:73517338-73517339	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs368528518	chr9:73517340-73517341	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs76380090	chr9:73517411-73517412	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs150275036	chr9:73517440-73517441	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs372160726	chr9:73517441-73517442	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs532237966	chr9:73517446-73517447	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs372862278	chr9:73517526-73517527	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs76690304	chr9:73517573-73517574	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs528324226	chr9:73517600-73517601	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs187564106	chr9:73517607-73517608	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs561777108	chr9:73517610-73517611	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs192568145	chr9:73517622-73517623	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs117572624	chr9:73517673-73517674	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs556306756	chr9:73517699-73517700	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs550433057	chr9:73517701-73517702	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs562590415	chr9:73517737-73517738	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs532978355	chr9:73517756-73517757	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs569790892	chr9:73517767-73517768	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs571168178	chr9:73517814-73517815	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs535377441	chr9:73517830-73517831	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs114640835	chr9:73517831-73517832	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs568588933	chr9:73517843-73517844	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs114797871	chr9:73517851-73517852	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs370847495	chr9:73517901-73517902	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs185176705	chr9:73517902-73517903	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs115487434	chr9:73517912-73517913	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs539452390	chr9:73517937-73517938	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs557690185	chr9:73517938-73517939	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs139279423	chr9:73517970-73517971	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs149806831	chr9:73517995-73517996	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs539120083	chr9:73518078-73518079	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs558792742	chr9:73518088-73518089	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs12349493	chr9:73518104-73518105	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs145756637	chr9:73518145-73518146	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs572438008	chr9:73518157-73518158	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs544362267	chr9:73518161-73518162	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs190100409	chr9:73518257-73518258	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs562572921	chr9:73518292-73518293	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs533016677	chr9:73518293-73518294	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs551489593	chr9:73518335-73518336	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Malignant melanoma	17260012	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:326 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:73508600-73519800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr9:73515600-73517600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr9:73515600-73517800	Enhancers	NHDF-Ad	bronchial
4	chr9:73515800-73517600	Enhancers	HUVEC	blood vessel
5	chr9:73515800-73517800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr9:73516000-73517800	Enhancers	HSMM	muscle
7	chr9:73516000-73517800	Enhancers	NH-A	brain
8	chr9:73516000-73518000	Enhancers	Fetal Kidney	kidney
9	chr9:73516000-73518200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr9:73516000-73518200	Enhancers	NHLF	lung
11	chr9:73516000-73518400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr9:73516000-73518400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr9:73516200-73517200	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr9:73516600-73517600	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr9:73516600-73517800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr9:73516600-73518000	Enhancers	Stomach Mucosa	stomach
17	chr9:73516800-73517200	Flanking Active TSS	NHEK	skin
18	chr9:73516800-73517400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr9:73516800-73517400	Enhancers	Fetal Heart	heart
20	chr9:73516800-73517800	Enhancers	Osteobl	bone
21	chr9:73516800-73518000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr9:73516800-73518400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr9:73516800-73518400	Flanking Active TSS	HMEC	breast
24	chr9:73516800-73518600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr9:73517000-73517200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr9:73517000-73517400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
27	chr9:73517000-73517400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr9:73517000-73517400	Enhancers	Duodenum Mucosa	Duodenum
29	chr9:73517000-73517600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr9:73517000-73517600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr9:73517000-73517600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr9:73517000-73517800	Enhancers	Placenta Amnion	Placenta Amnion
33	chr9:73517000-73518000	Enhancers	H9 Cell Line	embryonic stem cell
34	chr9:73517000-73518200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr9:73517000-73518400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr9:73517000-73518400	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr9:73517200-73517400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr9:73517200-73517600	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr9:73517200-73517800	Enhancers	NHEK	skin
40	chr9:73517200-73518000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr9:73517200-73518200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr9:73517200-73518200	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr9:73517200-73518200	Enhancers	Brain Anterior Caudate	brain
44	chr9:73517200-73518200	Enhancers	Brain Hippocampus Middle	brain
45	chr9:73517200-73518400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr9:73517200-73518400	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr9:73517400-73517600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr9:73517400-73517600	Weak transcription	Duodenum Mucosa	Duodenum
49	chr9:73517400-73517600	Enhancers	HSMMtube	muscle
50	chr9:73517400-73517800	Enhancers	Muscle Satellite Cultured Cells	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links