Variant report

Variant	nsv872550
Chromosome Location	chr1:173913804-173964206
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:244)
CpG islands
(count:183)
Chromatin interactive
region (count:44)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr1:173945708-173945746	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr1:173938988-173939273	K562	blood:	n/a	chr1:173939131-173939142
3	CEBPB	chr1:173946383-173946584	IMR90	lung:	n/a	n/a
4	CEBPB	chr1:173936372-173936563	HepG2	liver:	n/a	chr1:173936505-173936517 chr1:173936408-173936419
5	CEBPB	chr1:173939074-173939239	IMR90	lung:	n/a	chr1:173939131-173939142
6	CEBPB	chr1:173932853-173932923	K562	blood:	n/a	n/a
7	CEBPB	chr1:173939110-173939265	HepG2	liver:	n/a	chr1:173939131-173939142
8	CTCF	chr1:173943260-173943410	HCM	heart:	n/a	n/a
9	CTCF	chr1:173943333-173943398	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr1:173943320-173943470	Caco-2	colon:	n/a	n/a
11	CTCF	chr1:173943338-173943378	Fibrobl	skin:	n/a	n/a
12	CTCF	chr1:173939300-173939450	MCF-7	breast:	n/a	n/a
13	CTCF	chr1:173943100-173943250	HCPEpiC	choroid plexus:	n/a	n/a
14	CTCF	chr1:173943380-173943530	MCF-7	breast:	n/a	n/a
15	CTCF	chr1:173943301-173943415	MCF-7	breast:	n/a	n/a
16	CTCF	chr1:173939609-173939745	MCF-7	breast:	n/a	n/a
17	CTCF	chr1:173922931-173922951	Fibrobl	skin:	n/a	n/a
18	CTCF	chr1:173918541-173918653	GM13976	blood:	n/a	n/a
19	CTCF	chr1:173943302-173943416	MCF-7	breast:	n/a	n/a
20	CTCF	chr1:173943360-173943510	AG09319	gingival:	n/a	n/a
21	CTCF	chr1:173943299-173943414	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:173943300-173943450	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr1:173960060-173960210	GM12868	blood:	n/a	n/a
24	CTCF	chr1:173943330-173943379	Gliobla	brain:	n/a	n/a
25	CTCF	chr1:173943360-173943510	HMEC	breast:	n/a	n/a
26	CTCF	chr1:173943340-173943490	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr1:173939616-173939741	MCF-7	breast:	n/a	n/a
28	CTCF	chr1:173925280-173925430	GM12868	blood:	n/a	n/a
29	CTCF	chr1:173943320-173943470	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr1:173943320-173943470	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr1:173943314-173943397	NHEK	skin:	n/a	n/a
32	CTCF	chr1:173943320-173943470	AG10803	skin:	n/a	n/a
33	CTCF	chr1:173943380-173943530	HAc	cerebellar:	n/a	n/a
34	CTCF	chr1:173916700-173916850	GM12869	blood:	n/a	n/a
35	CTCF	chr1:173943380-173943530	AG04450	lung:	n/a	n/a
36	CTCF	chr1:173943240-173943390	GM12872	blood:	n/a	n/a
37	CTCF	chr1:173943340-173943490	Caco-2	colon:	n/a	n/a
38	CTCF	chr1:173943360-173943510	MCF-7	breast:	n/a	n/a
39	CTCF	chr1:173943380-173943530	BJ	skin:	n/a	n/a
40	CTCF	chr1:173943380-173943530	HFF	foreskin:	n/a	n/a
41	CTCF	chr1:173943360-173943510	BE2_C	brain:	n/a	n/a
42	CTCF	chr1:173943320-173943470	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr1:173943292-173943420	MCF-7	breast:	n/a	n/a
44	CTCF	chr1:173926107-173926142	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:173943320-173943470	HCFaa	heart:	n/a	n/a
46	CTCF	chr1:173943289-173943431	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:173939659-173939722	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:173922904-173922929	Fibrobl	skin:	n/a	n/a
49	CTCF	chr1:173943240-173943390	HMEC	breast:	n/a	n/a
50	CTCF	chr1:173922449-173922462	Medullo	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:173961904-173961954	GM12891	blood:	n/a
2	chr1:173934066-173934116	NHBE	bronchial:	n/a
3	chr1:173961904-173961954	HRCEpiC	kidney:	n/a
4	chr1:173934066-173934116	Jurkat	blood:	n/a
5	chr1:173930183-173930233	Caco-2	colon:	n/a
6	chr1:173961904-173961954	IMR90	lung:	fetal
7	chr1:173930183-173930233	SK-N-SH	brain:	n/a
8	chr1:173930183-173930233	SK-N-MC	brain:	n/a
9	chr1:173961904-173961954	CMK	blood:	n/a
10	chr1:173961904-173961954	GM12892	blood:	n/a
11	chr1:173934066-173934116	LNCaP	prostate:	n/a
12	chr1:173930183-173930233	HEEpiC	esophagus:	n/a
13	chr1:173934066-173934116	PANC-1	pancreas:	n/a
14	chr1:173934066-173934116	ovcar-3	ovarian:	n/a
15	chr1:173961904-173961954	NH-A	brain:	n/a
16	chr1:173930183-173930233	HPAEpiC	pulmonary alveolar:	n/a
17	chr1:173934066-173934116	Hepatocyte	liver:	n/a
18	chr1:173934066-173934116	AG09319	gingival:	n/a
19	chr1:173934066-173934116	AG04449	skin:	fetal
20	chr1:173930183-173930233	HCT-116	colon:	n/a
21	chr1:173961904-173961954	Hela-S3	cervix:	n/a
22	chr1:173934066-173934116	HAEpiC	amniotic membrane:	n/a
23	chr1:173934066-173934116	NH-A	brain:	n/a
24	chr1:173934066-173934116	MCF-7	breast:	n/a
25	chr1:173930183-173930233	HNPCEpiC	eye:	n/a
26	chr1:173934066-173934116	AG09309	skin:	n/a
27	chr1:173934066-173934116	HNPCEpiC	eye:	n/a
28	chr1:173930183-173930233	NH-A	brain:	n/a
29	chr1:173934066-173934116	GM06990	blood:	n/a
30	chr1:173930183-173930233	IMR90	lung:	fetal
31	chr1:173934066-173934116	PFSK-1	brain:	n/a
32	chr1:173934066-173934116	HIPEpiC	eye:	n/a
33	chr1:173930183-173930233	Hepatocyte	liver:	n/a
34	chr1:173961904-173961954	AG04449	skin:	fetal
35	chr1:173934066-173934116	HEEpiC	esophagus:	n/a
36	chr1:173930183-173930233	AG09319	gingival:	n/a
37	chr1:173961904-173961954	NB4	blood:	n/a
38	chr1:173930183-173930233	NHDF-neo	bronchial:	n/a
39	chr1:173961904-173961954	RPTEC	kidney:	n/a
40	chr1:173961904-173961954	ECC-1	luminal epithelium:	n/a
41	chr1:173934066-173934116	HL-60	blood:	n/a
42	chr1:173934066-173934116	AoSMC	blood vessel:	n/a
43	chr1:173961904-173961954	NT2-D1	testis:	n/a
44	chr1:173930183-173930233	HL-60	blood:	n/a
45	chr1:173934066-173934116	GM12892	blood:	n/a
46	chr1:173961904-173961954	PANC-1	pancreas:	n/a
47	chr1:173961904-173961954	AG09319	gingival:	n/a
48	chr1:173930183-173930233	ovcar-3	ovarian:	n/a
49	chr1:173934066-173934116	HepG2	liver:	n/a
50	chr1:173934066-173934116	SK-N-SH	brain:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:173916013..173918332-chr1:173921355..173923726,3	K562	blood:
2	chr1:173912141..173914805-chr1:173943938..173945745,2	K562	blood:
3	chr1:173927128..173928975-chr1:173932544..173934289,2	K562	blood:
4	chr1:173835118..173837073-chr1:173951885..173954734,2	K562	blood:
5	chr1:173954538..173956167-chr1:173959585..173961567,2	K562	blood:
6	chr1:173946530..173949481-chr1:173953639..173956535,2	MCF-7	breast:
7	chr1:173902831..173905140-chr1:173919125..173921351,2	K562	blood:
8	chr1:173931023..173932801-chr1:173933873..173936006,2	MCF-7	breast:
9	chr1:173919966..173923901-chr1:173923919..173927060,3	K562	blood:
10	chr1:173946530..173949481-chr1:173953639..173956535,2	MCF-7	breast:
11	chr1:173912141..173914805-chr1:173943938..173945745,2	K562	blood:
12	chr1:173833863..173839457-chr1:173910408..173918981,14	MCF-7	breast:
13	chr1:173941961..173943858-chr1:173944447..173947260,2	K562	blood:
14	chr1:173951301..173953436-chr1:173954526..173956321,2	K562	blood:
15	chr1:173941461..173943094-chr1:173945131..173947112,2	MCF-7	breast:
16	chr1:173923747..173925915-chr1:174209553..174212014,2	MCF-7	breast:
17	chr1:173931023..173932801-chr1:173933873..173936006,2	MCF-7	breast:
18	chr1:173932784..173934924-chr1:173990024..173992322,2	MCF-7	breast:
19	chr1:173959770..173961680-chr1:173990983..173993365,2	K562	blood:
20	chr1:173956360..173957903-chr1:173959725..173961914,2	K562	blood:
21	chr1:173835905..173838790-chr1:173929682..173932448,3	MCF-7	breast:
22	chr1:173939340..173940107-chr1:174043783..174044572,3	MCF-7	breast:
23	chr1:173954538..173956167-chr1:173959585..173961567,2	K562	blood:
24	chr1:173919966..173923901-chr1:173923919..173927060,3	K562	blood:
25	chr1:173929519..173931322-chr1:173931556..173934242,2	MCF-7	breast:
26	chr1:173956360..173957903-chr1:173959725..173961914,2	K562	blood:
27	chr1:173906434..173908742-chr1:173914028..173915858,2	K562	blood:
28	chr1:173961254..173963664-chr1:173990369..173993312,2	MCF-7	breast:
29	chr1:173941461..173943094-chr1:173945131..173947112,2	MCF-7	breast:
30	chr1:173931135..173933401-chr1:173937060..173938685,2	K562	blood:
31	chr1:173951363..173953301-chr1:173953950..173956185,2	K562	blood:
32	chr1:173936287..173938617-chr1:173989942..173991527,2	MCF-7	breast:
33	chr1:173835820..173838442-chr1:173925397..173927036,2	K562	blood:
34	chr1:173835394..173838931-chr1:173914614..173917379,4	MCF-7	breast:
35	chr1:173927128..173928975-chr1:173932544..173934289,2	K562	blood:
36	chr1:173829121..173831364-chr1:173963945..173965806,2	MCF-7	breast:
37	chr1:173875025..173877652-chr1:173913982..173916465,2	K562	blood:
38	chr1:173919788..173922130-chr1:173930099..173932471,2	MCF-7	breast:
39	chr1:173949574..173951674-chr1:173990214..173993126,3	MCF-7	breast:
40	chr1:173955497..173957436-chr1:173990257..173992230,2	MCF-7	breast:
41	chr1:173837529..173841751-chr1:173936779..173939459,3	K562	blood:
42	chr1:173941961..173943858-chr1:173944447..173947260,2	K562	blood:
43	chr1:173916013..173918332-chr1:173921355..173923726,3	K562	blood:
44	chr1:173948314..173951882-chr1:173977865..173981423,3	MCF-7	breast:

No data

Variant related genes	Relation type
RNA5SP68	TF binding region
RC3H1	TF binding region
RNA5SP68	CpG island
RC3H1	CpG island
ENSG00000185278	chromatin interactions
ENSG00000208317	chromatin interactions
ENSG00000135870	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000224977	chromatin interactions
ENSG00000200755	chromatin interactions

Extended variants
information (count: 1726 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1726 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1322781	chr1:173913804-173913805	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566978979	chr1:173913837-173913838	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs61828898	chr1:173913845-173913846	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs574547291	chr1:173913911-173913912	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs569161554	chr1:173913934-173913935	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs113901620	chr1:173913946-173913947	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs538193955	chr1:173913989-173913990	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs556530309	chr1:173914032-173914033	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs139503544	chr1:173914119-173914120	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs78999671	chr1:173914196-173914197	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs183792947	chr1:173914239-173914240	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs552757748	chr1:173914242-173914243	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs565210763	chr1:173914264-173914265	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs71718815	chr1:173914269-173914270	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs12063266	chr1:173914417-173914418	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs541612091	chr1:173914448-173914449	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs546224771	chr1:173914517-173914518	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs561908355	chr1:173914519-173914520	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs575598010	chr1:173914560-173914561	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs544550646	chr1:173914627-173914628	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs61828899	chr1:173914633-173914634	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs533148572	chr1:173914653-173914654	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs546989798	chr1:173914654-173914655	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs116383932	chr1:173914662-173914663	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs529394848	chr1:173914680-173914681	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs79988809	chr1:173914706-173914707	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs569149203	chr1:173914711-173914712	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs538134159	chr1:173914768-173914769	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs189283354	chr1:173914785-173914786	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs571622231	chr1:173914808-173914809	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs539022556	chr1:173914819-173914820	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs552936506	chr1:173914827-173914828	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs199936325	chr1:173914852-173914853	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs551553727	chr1:173914854-173914855	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs566441709	chr1:173914871-173914872	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs571774711	chr1:173914881-173914882	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs535574113	chr1:173914910-173914911	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs555583678	chr1:173914953-173914954	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs575536658	chr1:173914981-173914982	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs544442514	chr1:173914989-173914990	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs141145413	chr1:173915006-173915007	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs577881565	chr1:173915023-173915024	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs540219334	chr1:173915025-173915026	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs12563099	chr1:173915035-173915036	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs375813450	chr1:173915036-173915037	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs529361017	chr1:173915044-173915045	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs118154539	chr1:173915068-173915069	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs75580199	chr1:173915083-173915084	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs150708176	chr1:173915099-173915100	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs182245728	chr1:173915132-173915133	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
Autism	22495309	CNVD
Breast cancer	21611746	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1427 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:173894600-173914400	Weak transcription	Right Ventricle	heart
2	chr1:173896400-173914400	Weak transcription	Pancreas	Pancrea
3	chr1:173898000-173915200	Weak transcription	Aorta	Aorta
4	chr1:173899400-173917400	Strong transcription	Duodenum Smooth Muscle	Duodenum
5	chr1:173899400-173927200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
6	chr1:173899400-173929600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:173899600-173923200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:173899800-173953800	Strong transcription	Primary T cells fromperipheralblood	blood
9	chr1:173900000-173929600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr1:173900000-173958600	Strong transcription	Rectal Mucosa Donor 31	rectum
11	chr1:173900000-173962400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr1:173900000-173966600	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr1:173900000-173968200	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr1:173900200-173966400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr1:173900400-173964600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:173900800-173963800	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr1:173901200-173931400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:173901400-173962200	Strong transcription	Duodenum Mucosa	Duodenum
19	chr1:173901600-173966400	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr1:173901600-173966400	Strong transcription	Dnd41	blood
21	chr1:173902200-173921200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr1:173902200-173928200	Strong transcription	Rectal Mucosa Donor 29	rectum
23	chr1:173902200-173954600	Strong transcription	Primary B cells from peripheral blood	blood
24	chr1:173902600-173954400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr1:173903200-173925000	Strong transcription	Fetal Muscle Trunk	muscle
26	chr1:173903200-173925600	Strong transcription	Primary T helper cells PMA-I stimulated	--
27	chr1:173903400-173915600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr1:173903400-173917400	Strong transcription	HUVEC	blood vessel
29	chr1:173903400-173927000	Strong transcription	Fetal Muscle Leg	muscle
30	chr1:173903400-173927000	Strong transcription	Fetal Thymus	thymus
31	chr1:173904000-173929200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr1:173904000-173966400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr1:173904800-173921400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr1:173904800-173921400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr1:173904800-173923200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr1:173904800-173954200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr1:173905000-173927000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr1:173905000-173938400	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr1:173905000-173962400	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr1:173905200-173954600	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr1:173906000-173920800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr1:173906000-173925600	Strong transcription	Placenta	Placenta
43	chr1:173906000-173940400	Strong transcription	Adipose Nuclei	Adipose
44	chr1:173906000-173959000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr1:173906200-173920200	Strong transcription	Muscle Satellite Cultured Cells	--
46	chr1:173906200-173920400	Strong transcription	Skeletal Muscle Male	skeletal muscle
47	chr1:173906200-173921400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr1:173906200-173937600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr1:173906400-173931800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr1:173906800-173918400	Strong transcription	iPS-18 Cell Line	embryonic stem cell

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