Variant report

Variant	nsv427675
Chromosome Location	chr1:76070382-76187748
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1172)
CpG islands
(count:1526)
Chromatin interactive
region (count:93)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1172 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:76156263-76156463	K562	blood:	n/a	n/a
2	ARID3A	chr1:76138415-76138772	K562	blood:	n/a	n/a
3	ARID3A	chr1:76127609-76127665	K562	blood:	n/a	n/a
4	ARID3A	chr1:76143217-76143395	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:76105897-76106242	K562	blood:	n/a	n/a
6	ARID3A	chr1:76142701-76143423	K562	blood:	n/a	n/a
7	ARID3A	chr1:76172923-76173341	K562	blood:	n/a	n/a
8	ARID3A	chr1:76082080-76082152	HepG2	liver:	n/a	n/a
9	ATF1	chr1:76172970-76173277	K562	blood:	n/a	n/a
10	ATF1	chr1:76080039-76080344	K562	blood:	n/a	n/a
11	ATF1	chr1:76156227-76156551	K562	blood:	n/a	n/a
12	ATF1	chr1:76109354-76109542	K562	blood:	n/a	n/a
13	ATF1	chr1:76082531-76082931	K562	blood:	n/a	n/a
14	ATF1	chr1:76139698-76139874	K562	blood:	n/a	n/a
15	ATF1	chr1:76105885-76106222	K562	blood:	n/a	n/a
16	ATF2	chr1:76095599-76095993	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr1:76138498-76138845	K562	blood:	n/a	n/a
18	BACH1	chr1:76080097-76080757	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr1:76138455-76138930	K562	blood:	n/a	n/a
20	BACH1	chr1:76082259-76082774	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr1:76137820-76137966	K562	blood:	n/a	n/a
22	BACH1	chr1:76137871-76139155	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCLAF1	chr1:76172926-76173291	K562	blood:	n/a	n/a
24	BHLHE40	chr1:76098240-76098424	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:76105293-76105429	K562	blood:	n/a	n/a
26	BHLHE40	chr1:76172885-76173277	K562	blood:	n/a	n/a
27	BHLHE40	chr1:76107180-76107438	K562	blood:	n/a	n/a
28	BHLHE40	chr1:76082516-76082778	K562	blood:	n/a	n/a
29	BHLHE40	chr1:76137936-76138902	K562	blood:	n/a	n/a
30	BHLHE40	chr1:76105917-76106244	K562	blood:	n/a	n/a
31	BHLHE40	chr1:76186904-76187053	GM12878	blood:	n/a	n/a
32	BRCA1	chr1:76172998-76173358	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr1:76138437-76138629	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr1:76112759-76113226	K562	blood:	n/a	n/a
35	CBX3	chr1:76138277-76138932	K562	blood:	n/a	n/a
36	CBX3	chr1:76172760-76173391	K562	blood:	n/a	n/a
37	CCNT2	chr1:76159140-76159573	K562	blood:	n/a	chr1:76159162-76159171
38	CCNT2	chr1:76172904-76173197	K562	blood:	n/a	n/a
39	CCNT2	chr1:76156253-76156492	K562	blood:	n/a	n/a
40	CCNT2	chr1:76105959-76106219	K562	blood:	n/a	n/a
41	CCNT2	chr1:76081434-76081868	K562	blood:	n/a	n/a
42	CEBPB	chr1:76107129-76107469	K562	blood:	n/a	n/a
43	CEBPB	chr1:76151060-76151260	HepG2	liver:	n/a	chr1:76151076-76151087
44	CEBPB	chr1:76103067-76103358	K562	blood:	n/a	n/a
45	CEBPB	chr1:76123509-76123812	HepG2	liver:	n/a	chr1:76123673-76123684
46	CEBPB	chr1:76105433-76105469	K562	blood:	n/a	n/a
47	CEBPB	chr1:76151018-76151218	IMR90	lung:	n/a	chr1:76151076-76151087
48	CEBPB	chr1:76107117-76107372	K562	blood:	n/a	n/a
49	CEBPB	chr1:76080265-76080779	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr1:76097115-76097389	K562	blood:	n/a	chr1:76097287-76097298

(count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:76138023-76138073	HRE	kidney:	n/a
2	chr1:76138023-76138073	HRE	kidney:	n/a
3	chr1:76077832-76077882	HEK293	kidney:	embryo
4	chr1:76079177-76079227	HEEpiC	esophagus:	n/a
5	chr1:76079833-76079883	SK-N-SH_RA	brain:	n/a
6	chr1:76080727-76080777	HCM	heart:	n/a
7	chr1:76082888-76082938	GM12892	blood:	n/a
8	chr1:76080459-76080509	A549	lung:	n/a
9	chr1:76080924-76080974	GM12891	blood:	n/a
10	chr1:76080410-76080460	HUVEC	blood vessel:	n/a
11	chr1:76082173-76082223	HEK293	kidney:	embryo
12	chr1:76082690-76082740	GM12891	blood:	n/a
13	chr1:76082690-76082740	Caco-2	colon:	n/a
14	chr1:76138023-76138073	MCF-7	breast:	n/a
15	chr1:76081962-76082012	U87	brain:	n/a
16	chr1:76082690-76082740	HMEC	breast:	n/a
17	chr1:76085151-76085201	PrEC	prostate:	n/a
18	chr1:76080727-76080777	HCPEpiC	choroid plexus:	n/a
19	chr1:76080459-76080509	HCT-116	colon:	n/a
20	chr1:76078176-76078226	PANC-1	pancreas:	n/a
21	chr1:76081272-76081322	SKMC	muscle:	n/a
22	chr1:76080684-76080734	HMEC	breast:	n/a
23	chr1:76082568-76082618	NHBE	bronchial:	n/a
24	chr1:76085151-76085201	BE2_C	brain:	n/a
25	chr1:76082066-76082116	HIPEpiC	eye:	n/a
26	chr1:76085151-76085201	SK-N-SH	brain:	n/a
27	chr1:76078176-76078226	HMEC	breast:	n/a
28	chr1:76080727-76080777	AG04450	lung:	fetal
29	chr1:76095838-76095888	ECC-1	luminal epithelium:	n/a
30	chr1:76081272-76081322	HCF	heart:	n/a
31	chr1:76081408-76081458	NB4	blood:	n/a
32	chr1:76080410-76080460	HCT-116	colon:	n/a
33	chr1:76085151-76085201	Hepatocyte	liver:	n/a
34	chr1:76080727-76080777	U87	brain:	n/a
35	chr1:76081379-76081429	NH-A	brain:	n/a
36	chr1:76080727-76080777	NH-A	brain:	n/a
37	chr1:76082690-76082740	Hepatocyte	liver:	n/a
38	chr1:76082173-76082223	GM12892	blood:	n/a
39	chr1:76080459-76080509	GM12892	blood:	n/a
40	chr1:76082066-76082116	SK-N-SH	brain:	n/a
41	chr1:76082888-76082938	Jurkat	blood:	n/a
42	chr1:76082173-76082223	IMR90	lung:	fetal
43	chr1:76081962-76082012	H1-hESC	embryonic stem cell:	embryo
44	chr1:76082888-76082938	T-47D	breast:	n/a
45	chr1:76081408-76081458	U87	brain:	n/a
46	chr1:76095838-76095888	BJ	skin:	n/a
47	chr1:76081962-76082012	MCF-7	breast:	n/a
48	chr1:76078176-76078226	A549	lung:	n/a
49	chr1:76080294-76080344	ProgFib	skin:	n/a
50	chr1:76082066-76082116	HEEpiC	esophagus:	n/a

(count:93 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:76071710..76074403-chr1:76079679..76081378,2	K562	blood:
2	chr1:76182869..76185714-chr1:76255250..76257463,2	K562	blood:
3	chr1:76094932..76097642-chr1:76105459..76107452,2	K562	blood:
4	chr1:75984267..75985784-chr1:76081741..76084002,2	K562	blood:
5	chr1:75731173..75731698-chr1:76097693..76098339,2	MCF-7	breast:
6	chr1:76064706..76067511-chr1:76072450..76074334,2	K562	blood:
7	chr1:76184568..76187287-chr1:76187578..76190885,3	MCF-7	breast:
8	chr1:76177430..76180048-chr1:76194109..76196652,2	K562	blood:
9	chr1:76049895..76051572-chr1:76068803..76071353,2	K562	blood:
10	chr1:76168335..76170790-chr1:76173153..76175492,2	K562	blood:
11	chr1:76080033..76082466-chr1:76250224..76251859,2	MCF-7	breast:
12	chr1:76081387..76081887-chr15:39080643..39081147,2	Hela-S3	cervix:
13	chr1:76171538..76176296-chr1:76182594..76187669,7	K562	blood:
14	chr1:76079906..76082887-chr11:62607618..62609123,2	K562	blood:
15	chr1:76187424..76195796-chr1:76248839..76258922,52	K562	blood:
16	chr1:76083373..76085148-chr1:76086743..76089714,2	MCF-7	breast:
17	chr1:76136512..76138761-chr1:76260290..76263855,4	K562	blood:
18	chr1:76079907..76082887-chr11:62607623..62609125,2	K562	blood:
19	chr1:76139328..76142229-chr1:76158809..76161190,2	K562	blood:
20	chr1:76135232..76136937-chr1:76193196..76195615,2	K562	blood:
21	chr1:76154691..76156608-chr1:76251098..76253830,2	K562	blood:
22	chr1:76094932..76097642-chr1:76105459..76107452,2	K562	blood:
23	chr1:76178176..76179962-chr1:76184780..76186701,2	K562	blood:
24	chr1:76139328..76142229-chr1:76158809..76161190,2	K562	blood:
25	chr1:76157340..76160559-chr1:76189001..76191132,3	K562	blood:
26	chr1:76158932..76160525-chr1:76160690..76162510,2	K562	blood:
27	chr1:76140961..76144068-chr1:76250261..76252961,3	K562	blood:
28	chr1:76081802..76083861-chr1:76085137..76086923,2	K562	blood:
29	chr1:76178176..76179962-chr1:76184780..76186701,2	K562	blood:
30	chr1:76175057..76177134-chr1:76227565..76229242,2	K562	blood:
31	chr1:76103722..76106233-chr1:76108885..76111145,2	K562	blood:
32	chr1:76183392..76187625-chr1:76187644..76191545,4	MCF-7	breast:
33	chr1:76102793..76106233-chr1:76108594..76111145,3	K562	blood:
34	chr1:76116317..76118957-chr1:76120302..76123457,3	K562	blood:
35	chr1:76184645..76186917-chr1:76251532..76253531,2	K562	blood:
36	chr1:76066835..76069254-chr1:76079406..76081859,2	MCF-7	breast:
37	chr1:76136446..76138259-chr1:76189741..76191373,2	K562	blood:
38	chr1:76048770..76050841-chr1:76082825..76084870,2	MCF-7	breast:
39	chr1:76171538..76176296-chr1:76182594..76187669,7	K562	blood:
40	chr1:76153507..76155716-chr1:76158535..76161147,2	K562	blood:
41	chr1:76094259..76097858-chr1:76188776..76191867,4	K562	blood:
42	chr1:76153507..76155716-chr1:76158535..76161147,2	K562	blood:
43	chr1:76103722..76106233-chr1:76108885..76111145,2	K562	blood:
44	chr1:76171478..76174682-chr1:76188816..76193676,7	K562	blood:
45	chr1:76083373..76085148-chr1:76086743..76089714,2	MCF-7	breast:
46	chr1:76096029..76098574-chr1:76101114..76103972,2	K562	blood:
47	chr1:76098237..76098781-chr1:76108716..76109281,2	K562	blood:
48	chr1:76070009..76076148-chr1:76078248..76081967,7	K562	blood:
49	chr1:76081387..76082907-chr17:41398843..41401870,3	K562	blood:
50	chr1:76080604..76083289-chr1:76094142..76096069,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC44A5-4	chr1:76186030-76186090	XLOC_000872
2	lnc-SLC44A5-4	chr1:76175688-76176245	ENSG00000178193.5
3	lnc-SLC44A5-4	chr1:76143415-76143463	NONHSAT003985
4	lnc-SLC44A5-4	chr1:76186034-76186090	ENSG00000178193.5
5	lnc-SLC44A5-4	chr1:76174710-76174855	NONHSAT003984
6	lnc-SLC44A5-4	chr1:76107988-76108177	NONHSAT003985
7	lnc-SLC44A5-4	chr1:76186034-76186090	NONHSAT003984
8	lnc-SLC44A5-4	chr1:76103852-76104725	NONHSAT003984
9	lnc-SLC44A5-4	chr1:76105925-76108177	NONHSAT003984
10	lnc-SLC44A5-4	chr1:76175700-76176308	XLOC_000872

No data

Variant related genes	Relation type
ACADM	TF binding region
SLC44A5	TF binding region
ENSG00000230863	TF binding region
ACADM	CpG island
SLC44A5	CpG island
ENSG00000230863	CpG island
ENSG00000207241	chromatin interactions
ENSG00000206620	chromatin interactions
ENSG00000156873	chromatin interactions
ENSG00000201487	chromatin interactions
ENSG00000057468	chromatin interactions
ENSG00000137955	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000117054	chromatin interactions
ENSG00000178193	chromatin interactions

Extended variants
information (count: 2594 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:2594 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563265799	chr1:76070383-76070384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576930467	chr1:76070426-76070427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572174822	chr1:76070430-76070431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183427495	chr1:76070440-76070441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141120401	chr1:76070441-76070442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371103861	chr1:76070442-76070443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138272563	chr1:76070451-76070452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34812110	chr1:76070452-76070453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs211696	chr1:76070507-76070508	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs369079301	chr1:76070510-76070511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543051560	chr1:76070513-76070514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373385646	chr1:76070546-76070547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187750089	chr1:76070623-76070624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs193157228	chr1:76070662-76070663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376645520	chr1:76070704-76070705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185010705	chr1:76070744-76070745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559004426	chr1:76070830-76070831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199861076	chr1:76070928-76070929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370697297	chr1:76070932-76070933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375652471	chr1:76070933-76070934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368640650	chr1:76070934-76070935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142152041	chr1:76070945-76070946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551942866	chr1:76070994-76070995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570263386	chr1:76071005-76071006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs211697	chr1:76071011-76071012	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs549412559	chr1:76071031-76071032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567697746	chr1:76071101-76071102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188321406	chr1:76071143-76071144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530864665	chr1:76071174-76071175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553548816	chr1:76071188-76071189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113416343	chr1:76071217-76071218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2065481	chr1:76071271-76071272	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs539263966	chr1:76071317-76071318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570469911	chr1:76071323-76071324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557886524	chr1:76071394-76071395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs56253866	chr1:76071455-76071456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576281444	chr1:76071463-76071464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536915744	chr1:76071503-76071504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151278754	chr1:76071517-76071518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573333598	chr1:76071549-76071550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540621996	chr1:76071559-76071560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559063878	chr1:76071568-76071569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577627324	chr1:76071574-76071575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545276413	chr1:76071587-76071588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192599266	chr1:76071605-76071606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530995757	chr1:76071612-76071613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549725626	chr1:76071613-76071614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561564811	chr1:76071644-76071645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528533282	chr1:76071696-76071697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546972849	chr1:76071697-76071698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:740 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76070000-76078400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr1:76072400-76072600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:76072400-76072600	Enhancers	Fetal Brain Male	brain
4	chr1:76072600-76075200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr1:76072600-76077600	Weak transcription	Fetal Brain Male	brain
6	chr1:76077600-76079400	Enhancers	Fetal Brain Male	brain
7	chr1:76077800-76078000	Enhancers	Fetal Brain Female	brain
8	chr1:76078000-76078600	Active TSS	Fetal Brain Female	brain
9	chr1:76078400-76078800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:76078600-76079000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:76078600-76079000	Flanking Active TSS	Fetal Brain Female	brain
12	chr1:76078800-76079800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr1:76078800-76080600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:76079000-76079400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:76079000-76079400	Active TSS	Fetal Brain Female	brain
16	chr1:76079400-76079600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:76079400-76079600	Enhancers	Brain Germinal Matrix	brain
18	chr1:76079400-76079800	Flanking Active TSS	Fetal Brain Female	brain
19	chr1:76079400-76081400	Active TSS	Fetal Brain Male	brain
20	chr1:76079600-76080000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:76079600-76080000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:76079600-76080000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
23	chr1:76079600-76080200	Enhancers	Fetal Heart	heart
24	chr1:76079600-76080400	Flanking Active TSS	Brain Germinal Matrix	brain
25	chr1:76079600-76080600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
26	chr1:76079800-76080000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
27	chr1:76079800-76080000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:76079800-76080000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
29	chr1:76079800-76080000	Flanking Active TSS	Brain Anterior Caudate	brain
30	chr1:76079800-76080000	Flanking Active TSS	Brain Substantia Nigra	brain
31	chr1:76079800-76080200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr1:76079800-76080200	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr1:76079800-76080200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:76079800-76080200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr1:76079800-76080200	Active TSS	Brain Angular Gyrus	brain
36	chr1:76079800-76080200	Enhancers	Brain Cingulate Gyrus	brain
37	chr1:76079800-76080200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
38	chr1:76079800-76080400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
39	chr1:76079800-76080400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
40	chr1:76079800-76080400	Bivalent Enhancer	Stomach Mucosa	stomach
41	chr1:76079800-76081200	Active TSS	Fetal Brain Female	brain
42	chr1:76079800-76082200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
43	chr1:76079800-76082600	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr1:76080000-76080200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
45	chr1:76080000-76080200	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
46	chr1:76080000-76080200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
47	chr1:76080000-76080200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
48	chr1:76080000-76080200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr1:76080000-76080200	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr1:76080000-76080200	Active TSS	Brain Substantia Nigra	brain

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