Variant report

Variant	esv3316782
Chromosome Location	chr18:43676588-43677807
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	chr18:43677230-43677456	K562	blood:	n/a	n/a
2	ATF2	chr18:43677696-43678336	GM12878	blood:	n/a	n/a
3	BCLAF1	chr18:43677468-43678334	GM12878	blood:	n/a	n/a
4	BCLAF1	chr18:43677338-43678324	GM12878	blood:	n/a	n/a
5	CHD1	chr18:43676895-43678212	GM12878	blood:	n/a	n/a
6	CHD1	chr18:43677008-43678544	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr18:43677650-43678606	K562	blood:	n/a	n/a
8	CHD2	chr18:43677696-43678834	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr18:43677592-43678735	GM12878	blood:	n/a	n/a
10	CHD2	chr18:43677782-43679053	Hela-S3	cervix:	n/a	n/a
11	CTBP2	chr18:43677781-43678889	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr18:43677040-43677190	AG10803	skin:	n/a	n/a
13	CTCF	chr18:43677700-43677850	HEK293	kidney:	n/a	n/a
14	CTCF	chr18:43677780-43677930	BJ	skin:	n/a	n/a
15	CTCF	chr18:43677800-43678090	HBMEC	blood vessel:	n/a	n/a
16	CTCF	chr18:43676680-43676830	NHEK	skin:	n/a	n/a
17	CTCF	chr18:43677800-43677950	HMEC	breast:	n/a	n/a
18	EGR1	chr18:43677700-43678733	HCT-116	colon:	n/a	chr18:43678340-43678350 chr18:43678340-43678353 chr18:43678344-43678354 chr18:43678339-43678354 chr18:43678338-43678348 chr18:43678340-43678353 chr18:43678341-43678350 chr18:43678340-43678353
19	ELF1	chr18:43677732-43678335	GM12878	blood:	n/a	chr18:43678301-43678312 chr18:43678301-43678312 chr18:43678302-43678311
20	ELF1	chr18:43677675-43678310	GM12878	blood:	n/a	n/a
21	ELK1	chr18:43676919-43677059	K562	blood:	n/a	n/a
22	ELK1	chr18:43677756-43678465	Hela-S3	cervix:	n/a	n/a
23	EP300	chr18:43677098-43678279	GM12878	blood:	n/a	chr18:43677475-43677485
24	EP300	chr18:43677290-43677404	K562	blood:	n/a	n/a
25	EP300	chr18:43677122-43677877	GM12878	blood:	n/a	chr18:43677475-43677485
26	FOXM1	chr18:43677451-43678344	GM12878	blood:	n/a	n/a
27	FOXP2	chr18:43677799-43678358	PFSK-1	brain:	n/a	n/a
28	GABPA	chr18:43677737-43678948	HL-60	blood:	n/a	chr18:43678339-43678348 chr18:43678070-43678084
29	GABPA	chr18:43677742-43678788	K562	blood:	n/a	chr18:43678339-43678348 chr18:43678070-43678084
30	GABPA	chr18:43677779-43679053	MCF-7	breast:	n/a	chr18:43678339-43678348 chr18:43678070-43678084
31	GABPA	chr18:43677797-43678891	SK-N-SH	brain:	n/a	chr18:43678339-43678348 chr18:43678070-43678084
32	GTF2F1	chr18:43677644-43678680	Hela-S3	cervix:	n/a	n/a
33	HCFC1	chr18:43676574-43679241	Hela-S3	cervix:	n/a	n/a
34	HCFC1	chr18:43677564-43678786	K562	blood:	n/a	n/a
35	HEY1	chr18:43677476-43678311	K562	blood:	n/a	n/a
36	HEY1	chr18:43677805-43678839	HepG2	liver:	n/a	chr18:43678338-43678353
37	IKZF1	chr18:43676961-43677269	GM12878	blood:	n/a	n/a
38	IRF1	chr18:43676976-43678919	K562	blood:	n/a	chr18:43678335-43678349
39	IRF1	chr18:43677484-43677822	K562	blood:	n/a	n/a
40	MAFF	chr18:43677496-43678008	HepG2	liver:	n/a	n/a
41	MAX	chr18:43677436-43677598	K562	blood:	n/a	n/a
42	MAX	chr18:43677638-43678839	HCT-116	colon:	n/a	chr18:43678507-43678520 chr18:43678508-43678519 chr18:43678509-43678519 chr18:43678509-43678519 chr18:43678507-43678522 chr18:43678508-43678519 chr18:43678346-43678356 chr18:43678508-43678518 chr18:43678509-43678518 chr18:43678508-43678517
43	MAX	chr18:43677567-43679086	A549	lung:	n/a	chr18:43678507-43678520 chr18:43678508-43678519 chr18:43678509-43678519 chr18:43678509-43678519 chr18:43678507-43678522 chr18:43678508-43678519 chr18:43678346-43678356 chr18:43678508-43678518 chr18:43678509-43678518 chr18:43678508-43678517
44	MAX	chr18:43677393-43678862	HepG2	liver:	n/a	chr18:43678507-43678520 chr18:43678508-43678519 chr18:43678509-43678519 chr18:43678509-43678519 chr18:43678507-43678522 chr18:43678508-43678519 chr18:43678346-43678356 chr18:43678508-43678518 chr18:43678509-43678518 chr18:43678508-43678517
45	MAX	chr18:43677783-43678954	H1-hESC	embryonic stem cell:	n/a	chr18:43678507-43678520 chr18:43678508-43678519 chr18:43678509-43678519 chr18:43678509-43678519 chr18:43678507-43678522 chr18:43678508-43678519 chr18:43678346-43678356 chr18:43678508-43678518 chr18:43678509-43678518 chr18:43678508-43678517
46	MAX	chr18:43677764-43678730	K562	blood:	n/a	chr18:43678507-43678520 chr18:43678508-43678519 chr18:43678509-43678519 chr18:43678509-43678519 chr18:43678507-43678522 chr18:43678508-43678519 chr18:43678346-43678356 chr18:43678508-43678518 chr18:43678509-43678518 chr18:43678508-43678517
47	MAX	chr18:43677343-43678971	Hela-S3	cervix:	n/a	chr18:43678507-43678520 chr18:43678508-43678519 chr18:43678509-43678519 chr18:43678509-43678519 chr18:43678507-43678522 chr18:43678508-43678519 chr18:43678346-43678356 chr18:43678508-43678518 chr18:43678509-43678518 chr18:43678508-43678517
48	MAX	chr18:43677691-43678838	SK-N-SH	brain:	n/a	chr18:43678507-43678520 chr18:43678508-43678519 chr18:43678509-43678519 chr18:43678509-43678519 chr18:43678507-43678522 chr18:43678508-43678519 chr18:43678346-43678356 chr18:43678508-43678518 chr18:43678509-43678518 chr18:43678508-43678517
49	MAX	chr18:43677750-43679086	A549	lung:	n/a	chr18:43678507-43678520 chr18:43678508-43678519 chr18:43678509-43678519 chr18:43678509-43678519 chr18:43678507-43678522 chr18:43678508-43678519 chr18:43678346-43678356 chr18:43678508-43678518 chr18:43678509-43678518 chr18:43678508-43678517
50	MAX	chr18:43677802-43678861	SK-N-SH	brain:	n/a	chr18:43678507-43678520 chr18:43678508-43678519 chr18:43678509-43678519 chr18:43678509-43678519 chr18:43678507-43678522 chr18:43678508-43678519 chr18:43678346-43678356 chr18:43678508-43678518 chr18:43678509-43678518 chr18:43678508-43678517

No.	Distal block	Cell Line	Cell type
1	chr18:43676858..43680433-chr18:43682158..43685518,5	MCF-7	breast:
2	chr18:43676576..43678249-chr18:43751942..43754579,2	MCF-7	breast:
3	chr18:43669948..43672641-chr18:43676747..43679041,2	K562	blood:
4	chr18:43676160..43680812-chr18:43682051..43685941,8	K562	blood:
5	chr18:43545858..43548536-chr18:43676652..43678402,2	MCF-7	breast:
6	chr16:22448047..22448923-chr18:43677782..43678339,2	HCT-116	colon:
7	chr18:43669796..43671297-chr18:43673823..43676678,2	K562	blood:
8	chr18:43677240..43681670-chr18:43684014..43685946,4	K562	blood:
9	chr18:43671600..43674875-chr18:43675841..43678916,7	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HAUS1-1	chr18:43676293-43678434	NONHSAT059127

Variant related genes	Relation type
ATP5A1	TF binding region
ENSG00000152240	chromatin interactions
ENSG00000152223	chromatin interactions
ENSG00000237296	chromatin interactions
ENSG00000140743	chromatin interactions
ENSG00000152242	chromatin interactions
ENSG00000152234	chromatin interactions

Extended variants
information (count: 51 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:51 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374648518	chr18:43676600-43676601	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
2	rs570286122	chr18:43676614-43676615	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
3	rs190457081	chr18:43676626-43676627	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
4	rs10617047	chr18:43676645-43676646	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
5	rs375580885	chr18:43676646-43676647	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
6	rs552713375	chr18:43676680-43676681	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
7	rs183051496	chr18:43676700-43676701	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
8	rs2578183	chr18:43676720-43676721	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs552970258	chr18:43676722-43676723	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
10	rs111442315	chr18:43676735-43676736	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
11	rs186385644	chr18:43676768-43676769	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
12	rs535398818	chr18:43676778-43676779	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
13	rs566396309	chr18:43676847-43676848	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
14	rs556706885	chr18:43676873-43676874	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
15	rs60920014	chr18:43676897-43676898	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
16	rs2578184	chr18:43676915-43676916	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs541535825	chr18:43676949-43676950	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
18	rs71160709	chr18:43676968-43676969	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
19	rs2578185	chr18:43676972-43676973	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
20	rs2578186	chr18:43676975-43676976	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
21	rs374012405	chr18:43677135-43677136	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
22	rs150464061	chr18:43677150-43677151	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
23	rs2578187	chr18:43677151-43677152	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs572730732	chr18:43677265-43677266	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs182968874	chr18:43677280-43677281	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs561547357	chr18:43677281-43677282	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs187541622	chr18:43677316-43677317	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs76805885	chr18:43677319-43677320	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
29	rs138319097	chr18:43677321-43677322	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs199941889	chr18:43677342-43677343	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs142897574	chr18:43677361-43677362	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
32	rs552701198	chr18:43677384-43677385	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
33	rs568588365	chr18:43677439-43677440	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
34	rs146093758	chr18:43677453-43677454	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
35	rs534693041	chr18:43677455-43677456	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
36	rs370707569	chr18:43677462-43677463	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
37	rs116530480	chr18:43677494-43677495	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
38	rs139998178	chr18:43677529-43677530	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
39	rs535316250	chr18:43677534-43677535	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
40	rs556843974	chr18:43677537-43677538	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
41	rs377442698	chr18:43677550-43677551	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
42	rs539278820	chr18:43677558-43677559	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
43	rs192655464	chr18:43677561-43677562	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
44	rs572863567	chr18:43677675-43677676	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
45	rs539977510	chr18:43677726-43677727	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
46	rs74634459	chr18:43677748-43677749	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
47	rs183214508	chr18:43677760-43677761	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
48	rs187365158	chr18:43677790-43677791	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
49	rs34907121	chr18:43677793-43677794	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs368370550	chr18:43677797-43677798	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:43657800-43676600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr18:43670000-43676600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr18:43670400-43677200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr18:43670600-43676800	Weak transcription	Stomach Mucosa	stomach
5	chr18:43671800-43676600	Weak transcription	Fetal Kidney	kidney
6	chr18:43671800-43676600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr18:43671800-43676600	Weak transcription	NHLF	lung
8	chr18:43673200-43676600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr18:43673600-43676600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr18:43673800-43676600	Weak transcription	Colonic Mucosa	Colon
11	chr18:43673800-43676600	Weak transcription	Lung	lung
12	chr18:43673800-43676600	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr18:43673800-43676600	Weak transcription	Spleen	Spleen
14	chr18:43674000-43676600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr18:43674000-43677000	Enhancers	Fetal Brain Male	brain
16	chr18:43674400-43676600	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr18:43674400-43676600	Weak transcription	Gastric	stomach
18	chr18:43674600-43676600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr18:43674600-43678800	Active TSS	Right Atrium	heart
20	chr18:43674800-43676600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr18:43674800-43676800	Enhancers	Brain Substantia Nigra	brain
22	chr18:43675000-43676600	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr18:43675200-43676600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr18:43675200-43676600	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr18:43675200-43676600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr18:43675200-43676600	Enhancers	Adipose Nuclei	Adipose
27	chr18:43675200-43676600	Enhancers	Liver	Liver
28	chr18:43675200-43676600	Enhancers	Thymus	Thymus
29	chr18:43675400-43676600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr18:43675400-43676600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr18:43675400-43676600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr18:43675400-43676600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr18:43675400-43676600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr18:43675400-43676600	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr18:43675400-43676600	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr18:43675400-43676600	Enhancers	Pancreas	Pancrea
37	chr18:43675400-43676600	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr18:43675400-43676600	Weak transcription	A549	lung
39	chr18:43675400-43676600	Enhancers	HUVEC	blood vessel
40	chr18:43675400-43676600	Weak transcription	NH-A	brain
41	chr18:43675400-43676600	Weak transcription	NHDF-Ad	bronchial
42	chr18:43675400-43676800	Enhancers	Primary B cells from peripheral blood	blood
43	chr18:43675400-43678600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr18:43675600-43676600	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr18:43675600-43676600	Enhancers	Esophagus	oesophagus
46	chr18:43675600-43676600	Weak transcription	Fetal Lung	lung
47	chr18:43675600-43676600	Genic enhancers	Fetal Stomach	stomach
48	chr18:43675600-43676800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr18:43675600-43678600	Active TSS	Hela-S3	cervix
50	chr18:43675800-43676600	Weak transcription	H1 Cell Line	embryonic stem cell

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