Variant report

Variant	nsv1059892
Chromosome Location	chr17:34330315-34442620
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1250)
CpG islands
(count:1405)
Chromatin interactive
region (count:13)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1250 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:34334077-34334506	HepG2	liver:	n/a	n/a
2	ATF1	chr17:34361855-34362036	K562	blood:	n/a	n/a
3	ATF1	chr17:34426809-34426814	K562	blood:	n/a	n/a
4	ATF1	chr17:34361266-34361504	K562	blood:	n/a	n/a
5	ATF1	chr17:34341720-34341879	K562	blood:	n/a	n/a
6	ATF1	chr17:34430946-34431146	K562	blood:	n/a	n/a
7	ATF2	chr17:34416498-34418343	GM12878	blood:	n/a	n/a
8	ATF2	chr17:34430645-34431355	GM12878	blood:	n/a	n/a
9	ATF2	chr17:34401643-34402183	GM12878	blood:	n/a	n/a
10	ATF2	chr17:34419659-34420045	GM12878	blood:	n/a	n/a
11	ATF2	chr17:34399719-34400326	GM12878	blood:	n/a	n/a
12	ATF2	chr17:34430629-34431300	GM12878	blood:	n/a	n/a
13	ATF2	chr17:34419597-34420077	GM12878	blood:	n/a	n/a
14	ATF2	chr17:34409407-34410313	GM12878	blood:	n/a	n/a
15	ATF2	chr17:34399801-34400263	GM12878	blood:	n/a	n/a
16	ATF2	chr17:34416674-34418415	GM12878	blood:	n/a	n/a
17	BATF	chr17:34409388-34409730	GM12878	blood:	n/a	chr17:34409554-34409565
18	BATF	chr17:34419571-34419948	GM12878	blood:	n/a	n/a
19	BATF	chr17:34409941-34410426	GM12878	blood:	n/a	n/a
20	BATF	chr17:34401764-34402121	GM12878	blood:	n/a	chr17:34401893-34401904
21	BATF	chr17:34426557-34426883	GM12878	blood:	n/a	n/a
22	BATF	chr17:34426285-34426928	GM12878	blood:	n/a	n/a
23	BATF	chr17:34361127-34361501	GM12878	blood:	n/a	n/a
24	BATF	chr17:34401773-34402067	GM12878	blood:	n/a	chr17:34401893-34401904
25	BATF	chr17:34430738-34431209	GM12878	blood:	n/a	chr17:34431116-34431129
26	BATF	chr17:34417110-34418205	GM12878	blood:	n/a	n/a
27	BATF	chr17:34361202-34361551	GM12878	blood:	n/a	n/a
28	BATF	chr17:34419651-34420012	GM12878	blood:	n/a	n/a
29	BATF	chr17:34430667-34431449	GM12878	blood:	n/a	chr17:34431116-34431129
30	BATF	chr17:34409333-34409741	GM12878	blood:	n/a	chr17:34409554-34409565
31	BATF	chr17:34410017-34410366	GM12878	blood:	n/a	n/a
32	BATF	chr17:34417074-34418195	GM12878	blood:	n/a	n/a
33	BATF	chr17:34399711-34400204	GM12878	blood:	n/a	n/a
34	BCL11A	chr17:34430710-34431370	GM12878	blood:	n/a	n/a
35	BCL11A	chr17:34428651-34428982	GM12878	blood:	n/a	n/a
36	BCL11A	chr17:34414905-34415217	GM12878	blood:	n/a	chr17:34414981-34414990
37	BCL11A	chr17:34417122-34418147	GM12878	blood:	n/a	chr17:34418015-34418023
38	BCL11A	chr17:34361182-34361479	GM12878	blood:	n/a	n/a
39	BCL11A	chr17:34430653-34431272	GM12878	blood:	n/a	n/a
40	BCL11A	chr17:34414741-34415562	GM12878	blood:	n/a	chr17:34414981-34414990
41	BCL11A	chr17:34419681-34419983	GM12878	blood:	n/a	chr17:34419796-34419805 chr17:34419898-34419905
42	BCL11A	chr17:34401794-34402107	GM12878	blood:	n/a	n/a
43	BCL11A	chr17:34409980-34410339	GM12878	blood:	n/a	n/a
44	BCL11A	chr17:34361131-34361551	GM12878	blood:	n/a	n/a
45	BCL11A	chr17:34426380-34426887	GM12878	blood:	n/a	n/a
46	BCL11A	chr17:34409897-34410367	GM12878	blood:	n/a	n/a
47	BCL11A	chr17:34426528-34426740	GM12878	blood:	n/a	n/a
48	BCL11A	chr17:34417047-34418267	GM12878	blood:	n/a	chr17:34418015-34418023
49	BCL3	chr17:34417414-34418131	GM12878	blood:	n/a	chr17:34418015-34418023
50	BCL3	chr17:34419551-34419985	GM12878	blood:	n/a	chr17:34419796-34419805 chr17:34419898-34419905

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:34344416-34344466	SK-N-MC	brain:	n/a
2	chr17:34345172-34345222	SK-N-MC	brain:	n/a
3	chr17:34344416-34344466	SK-N-MC	brain:	n/a
4	chr17:34345172-34345222	SK-N-MC	brain:	n/a
5	chr17:34345172-34345222	HNPCEpiC	eye:	n/a
6	chr17:34434265-34434315	HRPEpiC	eye:	n/a
7	chr17:34390310-34390360	HUVEC	blood vessel:	n/a
8	chr17:34345172-34345222	GM12891	blood:	n/a
9	chr17:34434265-34434315	SAEC	small airway:	n/a
10	chr17:34344995-34345045	NB4	blood:	n/a
11	chr17:34429905-34429955	PANC-1	pancreas:	n/a
12	chr17:34344416-34344466	NB4	blood:	n/a
13	chr17:34429905-34429955	HCM	heart:	n/a
14	chr17:34344416-34344466	HRPEpiC	eye:	n/a
15	chr17:34417074-34417124	HEK293	kidney:	embryo
16	chr17:34345136-34345186	GM06990	blood:	n/a
17	chr17:34417434-34417484	GM12878	blood:	n/a
18	chr17:34432601-34432651	ProgFib	skin:	n/a
19	chr17:34391735-34391785	AG09319	gingival:	n/a
20	chr17:34391735-34391785	HEK293	kidney:	embryo
21	chr17:34391478-34391528	GM12891	blood:	n/a
22	chr17:34390628-34390678	GM12892	blood:	n/a
23	chr17:34346433-34346483	HNPCEpiC	eye:	n/a
24	chr17:34345392-34345442	GM12878	blood:	n/a
25	chr17:34394215-34394265	HNPCEpiC	eye:	n/a
26	chr17:34345392-34345442	T-47D	breast:	n/a
27	chr17:34345136-34345186	SK-N-SH	brain:	n/a
28	chr17:34345392-34345442	NB4	blood:	n/a
29	chr17:34344995-34345045	RPTEC	kidney:	n/a
30	chr17:34417530-34417580	BJ	skin:	n/a
31	chr17:34390628-34390678	ovcar-3	ovarian:	n/a
32	chr17:34430281-34430331	ECC-1	luminal epithelium:	n/a
33	chr17:34432601-34432651	HRE	kidney:	n/a
34	chr17:34430281-34430331	PANC-1	pancreas:	n/a
35	chr17:34434265-34434315	HCM	heart:	n/a
36	chr17:34417530-34417580	PANC-1	pancreas:	n/a
37	chr17:34344416-34344466	GM12891	blood:	n/a
38	chr17:34344416-34344466	ProgFib	skin:	n/a
39	chr17:34430281-34430331	LNCaP	prostate:	n/a
40	chr17:34390310-34390360	NHBE	bronchial:	n/a
41	chr17:34345136-34345186	HUVEC	blood vessel:	n/a
42	chr17:34390310-34390360	SK-N-SH	brain:	n/a
43	chr17:34415818-34415868	GM12878	blood:	n/a
44	chr17:34346381-34346431	SK-N-SH	brain:	n/a
45	chr17:34432841-34432891	HEK293	kidney:	embryo
46	chr17:34417074-34417124	HAEpiC	amniotic membrane:	n/a
47	chr17:34434265-34434315	PrEC	prostate:	n/a
48	chr17:34330410-34330460	HRPEpiC	eye:	n/a
49	chr17:34344995-34345045	HRE	kidney:	n/a
50	chr17:34391735-34391785	IMR90	lung:	fetal

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:34339180..34340890-chr17:34344090..34346721,2	K562	blood:
2	chr17:34339180..34340890-chr17:34344090..34346721,2	K562	blood:
3	chr17:34302767..34303445-chr17:34399612..34400175,2	K562	blood:
4	chr17:34397070..34399357-chr17:34401561..34403872,2	K562	blood:
5	chr17:34359094..34361696-chr17:34362624..34365203,2	K562	blood:
6	chr17:34359094..34361696-chr17:34362624..34365203,2	K562	blood:
7	chr17:34398060..34401079-chr2:11680489..11683465,4	MCF-7	breast:
8	chr17:34389572..34391840-chr17:34397915..34400017,2	MCF-7	breast:
9	chr17:34363677..34365239-chr17:34371843..34374735,2	K562	blood:
10	chr17:34397591..34400007-chr17:34404548..34407426,3	K562	blood:
11	chr17:34417985..34420053-chr17:34421112..34423520,2	K562	blood:
12	chr17:34417985..34420053-chr17:34421112..34423520,2	K562	blood:
13	chr17:34363677..34365239-chr17:34371843..34374735,2	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCL23-1	chr17:34365072-34365175	XLOC_012449
2	lnc-CCL18-1	chr17:34402643-34402735	ENSG00000224298.2
3	lnc-CCL18-1	chr17:34400226-34400308	ENSG00000224298.2
4	lnc-CCL3-1	chr17:34416678-34417480	NONHSAT053175
5	lnc-CCL18-4	chr17:34339544-34339931	ENSG00000267431.1
6	lnc-CCL4-1	chr17:34437543-34437838	NONHSAT053179
7	lnc-CCL18-1	chr17:34415639-34415957	ENSG00000224298.2
8	lnc-CCL18-5	chr17:34336602-34336723	ENSG00000267566.1
9	lnc-CCL3-1	chr17:34415639-34415952	NONHSAT053175
10	lnc-CCL18-5	chr17:34337060-34337452	ENSG00000267566.1
11	lnc-CCL23-1	chr17:34367780-34367984	XLOC_012449
12	lnc-CCL18-1	chr17:34401996-34402208	ENSG00000224298.2
13	lnc-CCL4-2	chr17:34439685-34442216	NONHSAT053180
14	lnc-CCL18-5	chr17:34337060-34338658	ENSG00000267566.1
15	lnc-CCL18-1	chr17:34404070-34404162	ENSG00000224298.2
16	lnc-CCL18-1	chr17:34401016-34401031	ENSG00000224298.2
17	lnc-CCL18-1	chr17:34416892-34417208	ENSG00000224298.1
18	lnc-CCL18-1	chr17:34408992-34409067	ENSG00000224298.1
19	lnc-CCL18-1	chr17:34408854-34408870	ENSG00000224298.2
20	lnc-CCL18-1	chr17:34416892-34417203	ENSG00000224298.2
21	lnc-CCL18-1	chr17:34401996-34402208	ENSG00000224298.2
22	lnc-CCL18-1	chr17:34400238-34400308	ENSG00000224298.2
23	lnc-CCL18-1	chr17:34416685-34417480	ENSG00000224298.2

No data

Variant related genes	Relation type
CCL18	TF binding region
ENSG00000267118	TF binding region
CCL23	TF binding region
ENSG00000267566	TF binding region
CCL3	TF binding region
CCL14	TF binding region
ENSG00000267431	TF binding region
CCL15	TF binding region
ENSG00000224298	TF binding region
CCL15-CCL14	TF binding region
RN7SL301P	TF binding region
CCL4	TF binding region
CCL18	CpG island
ENSG00000267118	CpG island
CCL23	CpG island
ENSG00000267566	CpG island
CCL3	CpG island
CCL14	CpG island
ENSG00000267431	CpG island
CCL15	CpG island
ENSG00000224298	CpG island
CCL15-CCL14	CpG island
RN7SL301P	CpG island
CCL4	CpG island
ENSG00000267431	chromatin interactions
ENSG00000167236	chromatin interactions
ENSG00000264010	chromatin interactions
ENSG00000006074	chromatin interactions
ENSG00000196208	chromatin interactions

Extended variants
information (count: 4532 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:4532 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543367224	chr17:34330366-34330367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569462977	chr17:34330402-34330403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374303037	chr17:34330409-34330410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78834229	chr17:34330411-34330412	Enhancers Weak transcription	CpG island	3 gene(s)	Overlapped CNVs	n/a
5	rs540836632	chr17:34330475-34330476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558928272	chr17:34330503-34330504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181412806	chr17:34330537-34330538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543894968	chr17:34330538-34330539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148351188	chr17:34330540-34330541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529903326	chr17:34330544-34330545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144286177	chr17:34330554-34330555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112512832	chr17:34330563-34330564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs71914010	chr17:34330570-34330571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs59189888	chr17:34330580-34330581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs56267816	chr17:34330581-34330582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189507571	chr17:34330669-34330670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76144420	chr17:34330678-34330679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs180987986	chr17:34330681-34330682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs71366497	chr17:34330698-34330699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs111614894	chr17:34330709-34330710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201643905	chr17:34330710-34330711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550776962	chr17:34330721-34330722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116271347	chr17:34330725-34330726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140152125	chr17:34330746-34330747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150327341	chr17:34330783-34330784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562537270	chr17:34330797-34330798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs137874740	chr17:34330809-34330810	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
28	rs567669219	chr17:34330840-34330841	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
29	rs60380956	chr17:34330883-34330884	Enhancers Weak transcription	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs143396430	chr17:34330893-34330894	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
31	rs573464376	chr17:34330915-34330916	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
32	rs185220168	chr17:34330925-34330926	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
33	rs558596409	chr17:34330939-34330940	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
34	rs116832492	chr17:34330949-34330950	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
35	rs539149663	chr17:34330950-34330951	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
36	rs531184535	chr17:34330951-34330952	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
37	rs75478034	chr17:34330965-34330966	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
38	rs75456429	chr17:34330987-34330988	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
39	rs111983437	chr17:34331002-34331003	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
40	rs375407945	chr17:34331003-34331004	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
41	rs147150892	chr17:34331026-34331027	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
42	rs73990617	chr17:34331045-34331046	Enhancers Weak transcription	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs73990618	chr17:34331084-34331085	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs191209799	chr17:34331116-34331117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576719814	chr17:34331147-34331148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532674218	chr17:34331157-34331158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532160521	chr17:34331160-34331161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183334540	chr17:34331177-34331178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187002694	chr17:34331182-34331183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530878188	chr17:34331194-34331195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:122)

Disease	PMID	Source
Melanoma	18172304	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	17603634	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Bladder cancer	19088036	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Meningioma	19431122	CNVD
Neurocytoma	17123091	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Cervical cancer	21062161	CNVD
Colorectal cancer	22860045	CNVD
Ductal carcinoma	18381933	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16417655	CNVD
Renal cysts	20603712	CNVD
Epilepsy	21858020	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Autism	20587423	CNVD
Renal cysts	20587423	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Mayer-Rokitansky-Kuster-Hauser syndrome	19889212	CNVD
Endometrial cancer	23636398	CNVD
Urothelial cell carcinoma	18451213	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	17850661	CNVD
Primary lung adenocarcinoma	16799635	CNVD
HIV/AIDS	18848619	CNVD
Rheumatoid arthritis	19220326	CNVD
Rheumatoid arthritis	18848619	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	18848619	CNVD
Type 1 diabetes	19220326	CNVD
HIV/AIDS	17330138	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Acute monocytic leukemia	16498392	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	18663149	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20932292	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Adrenocortical carcinoma	18281524	CNVD
Lung cancer	21569311	CNVD
Gastric cancer	21811585	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20824076	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:587 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:34327800-34332200	Enhancers	GM12878-XiMat	blood
2	chr17:34328000-34331000	Weak transcription	Small Intestine	intestine
3	chr17:34329200-34333400	Enhancers	Fetal Intestine Small	intestine
4	chr17:34329200-34333800	Enhancers	Fetal Intestine Large	intestine
5	chr17:34329200-34336400	Enhancers	HepG2	liver
6	chr17:34329400-34331400	Weak transcription	Fetal Kidney	kidney
7	chr17:34329600-34330400	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr17:34329600-34331400	Enhancers	Duodenum Mucosa	Duodenum
9	chr17:34329600-34332400	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr17:34329800-34331000	Weak transcription	Lung	lung
11	chr17:34329800-34332800	Weak transcription	Pancreas	Pancrea
12	chr17:34330000-34331200	Weak transcription	Stomach Mucosa	stomach
13	chr17:34330200-34330400	Enhancers	Colonic Mucosa	Colon
14	chr17:34330200-34335400	Enhancers	Liver	Liver
15	chr17:34330400-34330600	Enhancers	Rectal Mucosa Donor 29	rectum
16	chr17:34330600-34331400	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr17:34330800-34332400	Enhancers	Primary hematopoietic stem cells	blood
18	chr17:34331000-34331200	Enhancers	Lung	lung
19	chr17:34331000-34331200	Enhancers	Small Intestine	intestine
20	chr17:34331000-34331400	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr17:34331000-34332400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr17:34331000-34332400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr17:34331200-34331800	Weak transcription	Small Intestine	intestine
24	chr17:34331200-34332400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr17:34331200-34333800	Enhancers	Stomach Mucosa	stomach
26	chr17:34331400-34331600	Flanking Active TSS	Primary B cells from peripheral blood	blood
27	chr17:34331400-34332000	Enhancers	Fetal Kidney	kidney
28	chr17:34331400-34332200	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr17:34331400-34332400	Enhancers	Primary B cells from cord blood	blood
30	chr17:34331400-34332600	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr17:34331600-34332400	Enhancers	Primary B cells from peripheral blood	blood
32	chr17:34331800-34332000	Enhancers	Small Intestine	intestine
33	chr17:34331800-34332200	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr17:34332000-34332600	Weak transcription	Small Intestine	intestine
35	chr17:34332400-34333600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr17:34332400-34335600	Weak transcription	Primary B cells from peripheral blood	blood
37	chr17:34332800-34333000	Enhancers	Small Intestine	intestine
38	chr17:34332800-34333200	Enhancers	Pancreas	Pancrea
39	chr17:34333200-34334800	Weak transcription	Pancreas	Pancrea
40	chr17:34333400-34334800	Weak transcription	Fetal Intestine Small	intestine
41	chr17:34333600-34333800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr17:34333600-34333800	Enhancers	Duodenum Mucosa	Duodenum
43	chr17:34334800-34335000	Enhancers	Pancreas	Pancrea
44	chr17:34334800-34340800	ZNF genes & repeats	Fetal Intestine Small	intestine
45	chr17:34335400-34337200	Weak transcription	Liver	Liver
46	chr17:34335600-34336600	Enhancers	Primary B cells from peripheral blood	blood
47	chr17:34336000-34336400	Enhancers	GM12878-XiMat	blood
48	chr17:34336200-34336400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr17:34336200-34336600	Active TSS	K562	blood
50	chr17:34337000-34337200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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