Variant report

Variant	nsv976610
Chromosome Location	chr12:49577937-49580571
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:146)
CpG islands
(count:123)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:146 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr12:49578985-49579312	GM12878	blood:	n/a	n/a
2	CTCF	chr12:49579124-49579605	A549	lung:	n/a	n/a
3	CTCF	chr12:49579178-49579283	Spleen_OC	spleen:	n/a	n/a
4	CTCF	chr12:49580494-49580578	GM13976	blood:	n/a	n/a
5	CTCF	chr12:49579207-49579277	LNCaP	prostate:	n/a	n/a
6	CTCF	chr12:49579256-49579282	GM20000	blood:	n/a	n/a
7	EBF1	chr12:49579016-49579166	GM12878	blood:	n/a	n/a
8	EBF1	chr12:49578960-49579300	GM12878	blood:	n/a	n/a
9	EP300	chr12:49580326-49580663	GM12878	blood:	n/a	chr12:49580623-49580637
10	EP300	chr12:49578972-49579419	GM12878	blood:	n/a	n/a
11	GATA2	chr12:49578989-49579490	K562	blood:	n/a	n/a
12	HEY1	chr12:49580274-49580648	K562	blood:	n/a	n/a
13	HEY1	chr12:49580028-49580660	K562	blood:	n/a	n/a
14	HEY1	chr12:49578899-49579083	HepG2	liver:	n/a	n/a
15	HEY1	chr12:49579084-49579363	HepG2	liver:	n/a	n/a
16	HEY1	chr12:49578670-49579800	K562	blood:	n/a	n/a
17	HEY1	chr12:49578916-49579370	HepG2	liver:	n/a	n/a
18	HEY1	chr12:49578738-49579751	K562	blood:	n/a	n/a
19	IRF4	chr12:49578957-49579276	GM12878	blood:	n/a	n/a
20	JUND	chr12:49577058-49578092	SK-N-SH	brain:	n/a	n/a
21	JUND	chr12:49577260-49578171	SK-N-SH	brain:	n/a	n/a
22	MXI1	chr12:49579985-49584758	SK-N-SH	brain:	n/a	n/a
23	MXI1	chr12:49580546-49581674	IMR90	lung:	n/a	n/a
24	PAX5	chr12:49579174-49579428	GM12878	blood:	n/a	n/a
25	PAX5	chr12:49579064-49579706	GM12878	blood:	n/a	n/a
26	PBX3	chr12:49576977-49578130	SK-N-SH	brain:	n/a	n/a
27	PBX3	chr12:49577405-49578043	SK-N-SH	brain:	n/a	n/a
28	POLR2A	chr12:49579941-49579948	HUVEC	blood vessel:	n/a	n/a
29	POLR2A	chr12:49580293-49580632	GM12878	blood:	n/a	n/a
30	POLR2A	chr12:49578715-49579769	PFSK-1	brain:	n/a	n/a
31	POLR2A	chr12:49580214-49580530	HepG2	liver:	n/a	n/a
32	POLR2A	chr12:49580256-49580838	U87	brain:	n/a	n/a
33	POLR2A	chr12:49576930-49578155	HUVEC	blood vessel:	n/a	n/a
34	POLR2A	chr12:49577493-49578138	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr12:49578754-49579446	A549	lung:	n/a	n/a
36	POLR2A	chr12:49578993-49579160	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr12:49580460-49580612	A549	lung:	n/a	n/a
38	POLR2A	chr12:49578735-49579449	GM12878	blood:	n/a	n/a
39	POLR2A	chr12:49578367-49579450	SK-N-SH	brain:	n/a	n/a
40	POLR2A	chr12:49578744-49579295	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr12:49577076-49578294	HUVEC	blood vessel:	n/a	n/a
42	POLR2A	chr12:49578680-49579818	GM12891	blood:	n/a	n/a
43	POLR2A	chr12:49579958-49580692	GM12892	blood:	n/a	n/a
44	POLR2A	chr12:49578676-49579792	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr12:49580549-49584642	H1-neurons	neurons:	n/a	n/a
46	POLR2A	chr12:49580261-49580827	PFSK-1	brain:	n/a	n/a
47	POLR2A	chr12:49578810-49579520	U87	brain:	n/a	n/a
48	POLR2A	chr12:49578897-49579405	A549	lung:	n/a	n/a
49	POLR2A	chr12:49578939-49579080	Gliobla	brain:	n/a	n/a
50	POLR2A	chr12:49578545-49579887	GM12878	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:49579630-49579680	RPTEC	kidney:	n/a
2	chr12:49579630-49579680	RPTEC	kidney:	n/a
3	chr12:49580217-49580267	K562	blood:	n/a
4	chr12:49579630-49579680	GM06990	blood:	n/a
5	chr12:49580217-49580267	Hela-S3	cervix:	n/a
6	chr12:49580217-49580267	Jurkat	blood:	n/a
7	chr12:49579630-49579680	HCM	heart:	n/a
8	chr12:49579630-49579680	HMEC	breast:	n/a
9	chr12:49579630-49579680	PFSK-1	brain:	n/a
10	chr12:49579630-49579680	PrEC	prostate:	n/a
11	chr12:49580217-49580267	IMR90	lung:	fetal
12	chr12:49580217-49580267	PANC-1	pancreas:	n/a
13	chr12:49579630-49579680	HUVEC	blood vessel:	n/a
14	chr12:49580217-49580267	HIPEpiC	eye:	n/a
15	chr12:49580217-49580267	GM12892	blood:	n/a
16	chr12:49580217-49580267	HEEpiC	esophagus:	n/a
17	chr12:49580217-49580267	HCPEpiC	choroid plexus:	n/a
18	chr12:49579630-49579680	HAEpiC	amniotic membrane:	n/a
19	chr12:49579630-49579680	SK-N-MC	brain:	n/a
20	chr12:49580217-49580267	GM12878	blood:	n/a
21	chr12:49579630-49579680	SK-N-SH	brain:	n/a
22	chr12:49579630-49579680	GM12878	blood:	n/a
23	chr12:49580217-49580267	SK-N-SH	brain:	n/a
24	chr12:49579630-49579680	HepG2	liver:	n/a
25	chr12:49580217-49580267	SK-N-SH_RA	brain:	n/a
26	chr12:49580217-49580267	HCM	heart:	n/a
27	chr12:49580217-49580267	LNCaP	prostate:	n/a
28	chr12:49579630-49579680	HL-60	blood:	n/a
29	chr12:49579630-49579680	Jurkat	blood:	n/a
30	chr12:49580217-49580267	NH-A	brain:	n/a
31	chr12:49580217-49580267	NT2-D1	testis:	n/a
32	chr12:49580217-49580267	GM12891	blood:	n/a
33	chr12:49580217-49580267	PrEC	prostate:	n/a
34	chr12:49579630-49579680	HCT-116	colon:	n/a
35	chr12:49579630-49579680	GM12892	blood:	n/a
36	chr12:49579630-49579680	HRE	kidney:	n/a
37	chr12:49580217-49580267	HUVEC	blood vessel:	n/a
38	chr12:49580217-49580267	HRPEpiC	eye:	n/a
39	chr12:49579630-49579680	LNCaP	prostate:	n/a
40	chr12:49580217-49580267	AG04449	skin:	fetal
41	chr12:49579630-49579680	PANC-1	pancreas:	n/a
42	chr12:49580217-49580267	A549	lung:	n/a
43	chr12:49579630-49579680	CMK	blood:	n/a
44	chr12:49579630-49579680	Hela-S3	cervix:	n/a
45	chr12:49579630-49579680	HPAEpiC	pulmonary alveolar:	n/a
46	chr12:49580217-49580267	HL-60	blood:	n/a
47	chr12:49580217-49580267	ProgFib	skin:	n/a
48	chr12:49579630-49579680	IMR90	lung:	fetal
49	chr12:49580217-49580267	T-47D	breast:	n/a
50	chr12:49579630-49579680	AG04450	lung:	fetal

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:49523189..49526160-chr12:49580301..49583522,3	K562	blood:
2	chr12:49523810..49525846-chr12:49575368..49579813,5	K562	blood:
3	chr12:49524206..49526394-chr12:49575960..49578007,2	MCF-7	breast:
4	chr12:49455381..49457675-chr12:49576315..49579055,2	MCF-7	breast:
5	chr12:49577117..49578684-chr12:49582643..49584249,2	K562	blood:
6	chr12:49522685..49527255-chr12:49580115..49585539,18	MCF-7	breast:
7	chr12:49523732..49525684-chr12:49574789..49577975,3	K562	blood:
8	chr12:49521045..49522741-chr12:49576322..49578574,2	K562	blood:
9	chr12:49523298..49526534-chr12:49578242..49583023,5	K562	blood:

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	TUBA1A	hsa-miR-10a-5p	chr12:49578756-49578779
2	TUBA1A	hsa-miR-16-5p	chr12:49578772-49578766
3	TUBA1A	hsa-miR-16-5p	chr12:49578766-49578787

Variant related genes	Relation type
TUBA1C	TF binding region
TUBA1C	CpG island
ENSG00000258017	chromatin interactions
ENSG00000123416	chromatin interactions
ENSG00000167552	chromatin interactions
ENSG00000200309	chromatin interactions

Extended variants
information (count: 117 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:117 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557916301	chr12:49577950-49577951	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs74487599	chr12:49577957-49577958	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs553012488	chr12:49578012-49578013	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs556926129	chr12:49578064-49578065	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs573513531	chr12:49578111-49578112	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs12296189	chr12:49578118-49578119	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs559586349	chr12:49578119-49578120	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs528697062	chr12:49578127-49578128	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs12296265	chr12:49578128-49578129	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs7953169	chr12:49578172-49578173	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs531021645	chr12:49578202-49578203	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs530673877	chr12:49578250-49578251	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs550754746	chr12:49578276-49578277	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs372624920	chr12:49578334-49578335	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs566988766	chr12:49578355-49578356	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs139597300	chr12:49578376-49578377	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs180884019	chr12:49578418-49578419	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs139680402	chr12:49578419-49578420	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs549311843	chr12:49578469-49578470	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs565964017	chr12:49578494-49578495	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs550397299	chr12:49578504-49578505	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs569104720	chr12:49578527-49578528	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs140121590	chr12:49578582-49578583	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs1062441	chr12:49578619-49578620	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs557975791	chr12:49578647-49578648	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs1062440	chr12:49578661-49578662	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs571426354	chr12:49578669-49578670	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs150293856	chr12:49578679-49578680	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs556755463	chr12:49578680-49578681	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs1062439	chr12:49578687-49578688	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs11558066	chr12:49578706-49578707	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs185938303	chr12:49578767-49578768	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	Overlapped CNVs	n/a
33	rs1062437	chr12:49578780-49578781	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	Overlapped CNVs	n/a
34	rs371718931	chr12:49578784-49578785	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	Overlapped CNVs	n/a
35	rs200873943	chr12:49578802-49578803	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs1065730	chr12:49578810-49578811	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs11558069	chr12:49578829-49578830	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs137853050	chr12:49578884-49578885	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs137853049	chr12:49578885-49578886	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs11558070	chr12:49578886-49578887	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs11558065	chr12:49578891-49578892	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs137853047	chr12:49578893-49578894	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs201884190	chr12:49578895-49578896	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs3206694	chr12:49578901-49578902	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs137853044	chr12:49578944-49578945	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs1065724	chr12:49578946-49578947	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs137853048	chr12:49578959-49578960	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs199813289	chr12:49578982-49578983	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs200449362	chr12:49579035-49579036	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs140737357	chr12:49579054-49579055	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Cancer	17160897	CNVD
Cancer	20164919	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:49570600-49581000	Weak transcription	GM12878-XiMat	blood
2	chr12:49570800-49578400	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr12:49574200-49578600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr12:49574200-49580600	Weak transcription	Primary B cells from cord blood	blood
5	chr12:49575000-49578400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr12:49575200-49578200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr12:49575200-49578800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr12:49575800-49578000	Weak transcription	Fetal Stomach	stomach
9	chr12:49575800-49578200	Weak transcription	Fetal Lung	lung
10	chr12:49576000-49578200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr12:49576000-49578200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr12:49576000-49578200	Weak transcription	Fetal Intestine Large	intestine
13	chr12:49576000-49578600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr12:49576000-49580800	Weak transcription	A549	lung
15	chr12:49576200-49578000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr12:49576200-49578200	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr12:49576200-49578600	Weak transcription	Placenta	Placenta
18	chr12:49576200-49579200	Weak transcription	Fetal Intestine Small	intestine
19	chr12:49576200-49580800	Weak transcription	Fetal Kidney	kidney
20	chr12:49576400-49578000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr12:49576400-49578000	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr12:49576400-49578000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr12:49576400-49578000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr12:49576400-49578000	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr12:49576400-49578200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:49576400-49578200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr12:49576400-49578400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr12:49576400-49578600	Weak transcription	Aorta	Aorta
29	chr12:49576400-49578800	Weak transcription	Brain Substantia Nigra	brain
30	chr12:49576400-49578800	Weak transcription	Colon Smooth Muscle	Colon
31	chr12:49576400-49580000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr12:49576600-49578200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr12:49576600-49578200	Weak transcription	Spleen	Spleen
34	chr12:49576600-49578800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr12:49576800-49578400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr12:49576800-49578400	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr12:49576800-49578400	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr12:49576800-49578400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr12:49576800-49578400	Weak transcription	Duodenum Mucosa	Duodenum
40	chr12:49576800-49578400	Weak transcription	Dnd41	blood
41	chr12:49576800-49581800	Weak transcription	Liver	Liver
42	chr12:49577000-49578000	Weak transcription	Fetal Thymus	thymus
43	chr12:49577000-49578600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr12:49577000-49578600	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr12:49577000-49579200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr12:49577000-49579400	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr12:49577000-49580200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr12:49577000-49581600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr12:49577200-49578400	Weak transcription	HUVEC	blood vessel
50	chr12:49577200-49578600	Genic enhancers	Brain Anterior Caudate	brain

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