Variant report

Variant	esv1833433
Chromosome Location	chr9:71544920-71598165
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:768)
CpG islands
(count:61)
Chromatin interactive
region (count:28)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:71584469-71584970	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:71576402-71576900	K562	blood:	n/a	n/a
3	ARID3A	chr9:71598080-71598400	K562	blood:	n/a	n/a
4	ARID3A	chr9:71584464-71585376	K562	blood:	n/a	n/a
5	ATF1	chr9:71584518-71584727	K562	blood:	n/a	n/a
6	ATF1	chr9:71598096-71598406	K562	blood:	n/a	n/a
7	ATF1	chr9:71590616-71590989	K562	blood:	n/a	n/a
8	ATF1	chr9:71576511-71576777	K562	blood:	n/a	n/a
9	ATF2	chr9:71548349-71548993	GM12878	blood:	n/a	n/a
10	ATF2	chr9:71581453-71582017	GM12878	blood:	n/a	n/a
11	ATF2	chr9:71562782-71563303	GM12878	blood:	n/a	n/a
12	ATF2	chr9:71590432-71591070	GM12878	blood:	n/a	n/a
13	ATF2	chr9:71548216-71549106	GM12878	blood:	n/a	n/a
14	ATF2	chr9:71581505-71582024	GM12878	blood:	n/a	n/a
15	ATF2	chr9:71589185-71589864	GM12878	blood:	n/a	n/a
16	ATF2	chr9:71589241-71589855	GM12878	blood:	n/a	n/a
17	ATF2	chr9:71561786-71562440	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr9:71596689-71597229	GM12878	blood:	n/a	n/a
19	ATF2	chr9:71590514-71590994	GM12878	blood:	n/a	n/a
20	ATF2	chr9:71566854-71567581	GM12878	blood:	n/a	n/a
21	BACH1	chr9:71565650-71565999	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr9:71567800-71567984	GM12878	blood:	n/a	n/a
23	BATF	chr9:71567183-71567487	GM12878	blood:	n/a	n/a
24	BATF	chr9:71589267-71589756	GM12878	blood:	n/a	n/a
25	BATF	chr9:71567186-71567536	GM12878	blood:	n/a	n/a
26	BATF	chr9:71590609-71590951	GM12878	blood:	n/a	n/a
27	BATF	chr9:71581550-71581855	GM12878	blood:	n/a	n/a
28	BATF	chr9:71589019-71589887	GM12878	blood:	n/a	n/a
29	BATF	chr9:71562819-71563155	GM12878	blood:	n/a	chr9:71563078-71563091
30	BATF	chr9:71596762-71597136	GM12878	blood:	n/a	n/a
31	BATF	chr9:71548377-71548631	GM12878	blood:	n/a	n/a
32	BATF	chr9:71581476-71581895	GM12878	blood:	n/a	n/a
33	BCL11A	chr9:71581490-71581887	GM12878	blood:	n/a	n/a
34	BCL11A	chr9:71589287-71589748	GM12878	blood:	n/a	n/a
35	BCL11A	chr9:71561935-71562259	H1-hESC	embryonic stem cell:	n/a	n/a
36	BCL11A	chr9:71596784-71597119	GM12878	blood:	n/a	n/a
37	BCL11A	chr9:71561976-71562202	H1-hESC	embryonic stem cell:	n/a	n/a
38	BCL11A	chr9:71596778-71597163	GM12878	blood:	n/a	n/a
39	BCL3	chr9:71589285-71589775	GM12878	blood:	n/a	n/a
40	BCL3	chr9:71548345-71548717	GM12878	blood:	n/a	n/a
41	BCL3	chr9:71567095-71567504	GM12878	blood:	n/a	n/a
42	BCLAF1	chr9:71589234-71589849	GM12878	blood:	n/a	n/a
43	BCLAF1	chr9:71596671-71597179	GM12878	blood:	n/a	n/a
44	BCLAF1	chr9:71567049-71567546	GM12878	blood:	n/a	n/a
45	BCLAF1	chr9:71548216-71548848	GM12878	blood:	n/a	chr9:71548805-71548814
46	BHLHE40	chr9:71589274-71589847	GM12878	blood:	n/a	n/a
47	BHLHE40	chr9:71565142-71565395	GM12878	blood:	n/a	n/a
48	BHLHE40	chr9:71590642-71590888	K562	blood:	n/a	n/a
49	BHLHE40	chr9:71598077-71598395	K562	blood:	n/a	n/a
50	BHLHE40	chr9:71548240-71548736	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71589563-71589613	U87	brain:	n/a
2	chr9:71589563-71589613	HMEC	breast:	n/a
3	chr9:71589563-71589613	GM06990	blood:	n/a
4	chr9:71589563-71589613	SK-N-SH	brain:	n/a
5	chr9:71589563-71589613	K562	blood:	n/a
6	chr9:71589563-71589613	RPTEC	kidney:	n/a
7	chr9:71589563-71589613	AG09319	gingival:	n/a
8	chr9:71589563-71589613	HRPEpiC	eye:	n/a
9	chr9:71589563-71589613	NH-A	brain:	n/a
10	chr9:71589563-71589613	BJ	skin:	n/a
11	chr9:71589563-71589613	HCM	heart:	n/a
12	chr9:71589563-71589613	Hepatocyte	liver:	n/a
13	chr9:71589563-71589613	T-47D	breast:	n/a
14	chr9:71589563-71589613	GM19239	blood:	n/a
15	chr9:71589563-71589613	HIPEpiC	eye:	n/a
16	chr9:71589563-71589613	HPAEpiC	pulmonary alveolar:	n/a
17	chr9:71589563-71589613	IMR90	lung:	fetal
18	chr9:71589563-71589613	GM12878	blood:	n/a
19	chr9:71589563-71589613	AG09309	skin:	n/a
20	chr9:71589563-71589613	HRE	kidney:	n/a
21	chr9:71589563-71589613	GM12892	blood:	n/a
22	chr9:71589563-71589613	AG04449	skin:	fetal
23	chr9:71589563-71589613	HEK293	kidney:	embryo
24	chr9:71589563-71589613	ProgFib	skin:	n/a
25	chr9:71589563-71589613	HepG2	liver:	n/a
26	chr9:71589563-71589613	A549	lung:	n/a
27	chr9:71589563-71589613	PFSK-1	brain:	n/a
28	chr9:71589563-71589613	ovcar-3	ovarian:	n/a
29	chr9:71589563-71589613	MCF10A-Er-Src	breast:	n/a
30	chr9:71589563-71589613	SK-N-MC	brain:	n/a
31	chr9:71589563-71589613	HCF	heart:	n/a
32	chr9:71589563-71589613	HRCEpiC	kidney:	n/a
33	chr9:71589563-71589613	HL-60	blood:	n/a
34	chr9:71589563-71589613	H1-hESC	embryonic stem cell:	embryo
35	chr9:71589563-71589613	Caco-2	colon:	n/a
36	chr9:71589563-71589613	HUVEC	blood vessel:	n/a
37	chr9:71589563-71589613	SKMC	muscle:	n/a
38	chr9:71589563-71589613	AG10803	skin:	n/a
39	chr9:71589563-71589613	Hela-S3	cervix:	n/a
40	chr9:71589563-71589613	AG04450	lung:	fetal
41	chr9:71589563-71589613	HNPCEpiC	eye:	n/a
42	chr9:71589563-71589613	NHBE	bronchial:	n/a
43	chr9:71589563-71589613	HCT-116	colon:	n/a
44	chr9:71589563-71589613	LNCaP	prostate:	n/a
45	chr9:71589563-71589613	GM12891	blood:	n/a
46	chr9:71589563-71589613	SK-N-SH_RA	brain:	n/a
47	chr9:71589563-71589613	PrEC	prostate:	n/a
48	chr9:71589563-71589613	Jurkat	blood:	n/a
49	chr9:71589563-71589613	HEEpiC	esophagus:	n/a
50	chr9:71589563-71589613	PANC-1	pancreas:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:71577984..71579536-chr9:71582505..71585285,2	K562	blood:
2	chr9:71594449..71596709-chr9:71598735..71600800,2	K562	blood:
3	chr9:71590575..71592087-chr9:71593583..71595166,2	K562	blood:
4	chr9:71572197..71575075-chr9:71576543..71579524,4	K562	blood:
5	chr9:71545273..71547947-chr9:71556049..71558568,2	MCF-7	breast:
6	chr9:71577984..71579536-chr9:71582505..71585285,2	K562	blood:
7	chr9:71589348..71591998-chr9:71596121..71599178,3	K562	blood:
8	chr9:71491880..71494040-chr9:71553268..71555351,2	K562	blood:
9	chr9:71587606..71589215-chr9:71606682..71608603,2	MCF-7	breast:
10	chr9:71568914..71571612-chr9:71576098..71578241,2	K562	blood:
11	chr9:71590575..71592087-chr9:71593583..71595166,2	K562	blood:
12	chr9:71545273..71547947-chr9:71556049..71558568,2	MCF-7	breast:
13	chr9:71584135..71587170-chr9:71595047..71597666,3	K562	blood:
14	chr9:71576569..71578561-chr9:71582492..71584226,2	MCF-7	breast:
15	chr9:71577956..71581283-chr9:71582183..71585440,6	K562	blood:
16	chr9:71546260..71548319-chr9:71558934..71561181,2	K562	blood:
17	chr9:71573438..71576022-chr9:71576543..71579524,3	K562	blood:
18	chr9:71576569..71578561-chr9:71582492..71584226,2	MCF-7	breast:
19	chr9:71587881..71589909-chr9:71610346..71613287,2	K562	blood:
20	chr9:71568914..71571612-chr9:71576098..71578241,2	K562	blood:
21	chr9:71546260..71548319-chr9:71558934..71561181,2	K562	blood:
22	chr9:71568407..71571024-chr9:71572381..71575201,2	K562	blood:
23	chr9:71584135..71587170-chr9:71595047..71597666,3	K562	blood:
24	chr9:71589348..71591998-chr9:71596121..71599178,3	K562	blood:
25	chr9:71577956..71581283-chr9:71582183..71585440,6	K562	blood:
26	chr9:71573438..71576022-chr9:71576543..71579524,3	K562	blood:
27	chr9:71572197..71575075-chr9:71576543..71579524,4	K562	blood:
28	chr9:71568407..71571024-chr9:71572381..71575201,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKACG-5	chr9:71563250-71563521	expReg_chr9_3063_-
2	lnc-PRKACG-1	chr9:71570856-71572127	NONHSAT131759
3	lnc-PRKACG-1	chr9:71590580-71590757	ENSG00000249652
4	lnc-PRKACG-1	chr9:71590580-71590735	NONHSAT131759
5	lnc-PRKACG-1	chr9:71571942-71572127	ENSG00000249652
6	lnc-PRKACG-1	chr9:71568004-71569861	ENSG00000249652

No data

Variant related genes	Relation type
RNU6-820P	TF binding region
RNU6-820P	CpG island
SMAD7	miRNA target sites
NFIB	miRNA target sites
TRIP12	miRNA target sites

Extended variants
information (count: 1922 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1922 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577824798	chr9:71544924-71544925	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147308301	chr9:71544951-71544952	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76637272	chr9:71544957-71544958	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572285863	chr9:71544958-71544959	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369066589	chr9:71544976-71544977	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561255889	chr9:71545016-71545017	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs180687026	chr9:71545023-71545024	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543221936	chr9:71545030-71545031	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185399736	chr9:71545036-71545037	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140886087	chr9:71545039-71545040	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs117911594	chr9:71545049-71545050	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs71503645	chr9:71545058-71545059	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189342362	chr9:71545076-71545077	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs377537782	chr9:71545088-71545089	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563181964	chr9:71545107-71545108	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567979680	chr9:71545113-71545114	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538405806	chr9:71545190-71545191	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144330052	chr9:71545203-71545204	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370799897	chr9:71545221-71545222	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150732454	chr9:71545291-71545292	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538399253	chr9:71545344-71545345	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs60502138	chr9:71545380-71545381	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs571901666	chr9:71545390-71545391	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542631770	chr9:71545437-71545438	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376418564	chr9:71545477-71545478	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554535060	chr9:71545515-71545516	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200904392	chr9:71545517-71545518	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10869543	chr9:71545518-71545519	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs543191551	chr9:71545521-71545522	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564784457	chr9:71545541-71545542	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374487040	chr9:71545566-71545567	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146730497	chr9:71545591-71545592	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374303718	chr9:71545592-71545593	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs74533484	chr9:71545615-71545616	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373424418	chr9:71545629-71545630	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530160321	chr9:71545672-71545673	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145696886	chr9:71545673-71545674	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560637123	chr9:71545709-71545710	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78943163	chr9:71545710-71545711	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111327764	chr9:71545720-71545721	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549372445	chr9:71545756-71545757	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369548236	chr9:71545778-71545779	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181887526	chr9:71545802-71545803	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532069387	chr9:71545817-71545818	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139043920	chr9:71545820-71545821	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186531881	chr9:71545830-71545831	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552232205	chr9:71545863-71545864	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539228399	chr9:71545987-71545988	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547151419	chr9:71546012-71546013	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373029739	chr9:71546071-71546072	Strong transcription Weak transcription Enhancers	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
Melanoma	22183965	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
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD

Chromatin state (count:924 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71510400-71576200	Weak transcription	Stomach Mucosa	stomach
2	chr9:71512200-71548800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr9:71514200-71553600	Weak transcription	Aorta	Aorta
4	chr9:71514200-71557800	Weak transcription	Lung	lung
5	chr9:71519400-71573000	Weak transcription	Gastric	stomach
6	chr9:71532800-71556800	Weak transcription	Right Ventricle	heart
7	chr9:71535000-71569600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr9:71535200-71546000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr9:71535200-71547600	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr9:71535200-71555400	Weak transcription	Left Ventricle	heart
11	chr9:71535400-71546400	Weak transcription	GM12878-XiMat	blood
12	chr9:71535800-71547600	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr9:71536200-71548400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr9:71536400-71546200	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr9:71536600-71557400	Weak transcription	Colonic Mucosa	Colon
16	chr9:71542000-71551600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr9:71542200-71564400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr9:71542400-71549800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr9:71542400-71549800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr9:71543000-71553600	Weak transcription	Primary hematopoietic stem cells	blood
21	chr9:71543400-71545200	Strong transcription	Primary B cells from peripheral blood	blood
22	chr9:71543800-71545000	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr9:71543800-71545000	Weak transcription	K562	blood
24	chr9:71543800-71546600	Weak transcription	Pancreas	Pancrea
25	chr9:71543800-71547200	Strong transcription	Primary B cells from cord blood	blood
26	chr9:71544200-71545200	Strong transcription	Duodenum Mucosa	Duodenum
27	chr9:71544800-71545400	Strong transcription	Fetal Intestine Small	intestine
28	chr9:71544800-71545400	Strong transcription	HepG2	liver
29	chr9:71544800-71547800	Strong transcription	Fetal Intestine Large	intestine
30	chr9:71545000-71545200	Strong transcription	Rectal Mucosa Donor 31	rectum
31	chr9:71545000-71545400	Enhancers	K562	blood
32	chr9:71545000-71561600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr9:71545200-71545400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
34	chr9:71545200-71548000	Weak transcription	Primary B cells from peripheral blood	blood
35	chr9:71545200-71553600	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr9:71545400-71549600	Weak transcription	Fetal Intestine Small	intestine
37	chr9:71545400-71553600	Weak transcription	Duodenum Mucosa	Duodenum
38	chr9:71545400-71553600	Weak transcription	HepG2	liver
39	chr9:71545400-71562400	Weak transcription	K562	blood
40	chr9:71546000-71547200	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr9:71546000-71547200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr9:71546200-71546800	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr9:71546200-71547200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr9:71546200-71547200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr9:71546200-71547200	Enhancers	Dnd41	blood
46	chr9:71546200-71547400	Enhancers	Primary T cells from cord blood	blood
47	chr9:71546400-71547200	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr9:71546400-71547200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
49	chr9:71546400-71547200	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr9:71546400-71547200	Enhancers	Primary T killer memory cells from peripheral blood	blood

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