Variant report

Variant	esv3431172
Chromosome Location	chr12:31078685-31080783
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:68)
CpG islands
(count:367)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:68 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr12:31079297-31079429	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD1	chr12:31079467-31079488	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD2	chr12:31078905-31079452	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTBP2	chr12:31078500-31079604	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr12:31079360-31079510	HUVEC	blood vessel:	n/a	n/a
6	CTCF	chr12:31079340-31079490	HMEC	breast:	n/a	n/a
7	CTCF	chr12:31079320-31079470	HRE	kidney:	n/a	n/a
8	CTCF	chr12:31079400-31079550	AG04450	lung:	n/a	n/a
9	CTCF	chr12:31079320-31079470	HCPEpiC	choroid plexus:	n/a	n/a
10	CTCF	chr12:31079360-31079510	HRPEpiC	eye:	n/a	n/a
11	CTCF	chr12:31079380-31079530	AG09319	gingival:	n/a	n/a
12	CTCF	chr12:31079340-31079490	BJ	skin:	n/a	n/a
13	CTCF	chr12:31079160-31079310	HAc	cerebellar:	n/a	n/a
14	CTCF	chr12:31079420-31079570	HCM	heart:	n/a	chr12:31079543-31079551
15	CTCF	chr12:31079440-31079590	AG04449	skin:	n/a	chr12:31079543-31079551
16	CTCF	chr12:31079400-31079550	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr12:31079472-31079555	IMR90	lung:	n/a	chr12:31079543-31079551
18	CTCF	chr12:31079340-31079490	AG09319	gingival:	n/a	n/a
19	CTCF	chr12:31079380-31079530	HAc	cerebellar:	n/a	n/a
20	CTCF	chr12:31079340-31079490	HepG2	liver:	n/a	n/a
21	CTCF	chr12:31079360-31079510	RPTEC	kidney:	n/a	n/a
22	CTCF	chr12:31079240-31079390	AG04450	lung:	n/a	n/a
23	E2F6	chr12:31079061-31080402	H1-hESC	embryonic stem cell:	n/a	chr12:31079817-31079826 chr12:31079338-31079347 chr12:31079502-31079512 chr12:31079501-31079511
24	E2F6	chr12:31079705-31080226	H1-hESC	embryonic stem cell:	n/a	chr12:31079817-31079826
25	E2F6	chr12:31079119-31079669	H1-hESC	embryonic stem cell:	n/a	chr12:31079338-31079347 chr12:31079502-31079512 chr12:31079501-31079511
26	GTF2F1	chr12:31079222-31079571	H1-hESC	embryonic stem cell:	n/a	n/a
27	JUN	chr12:31078762-31078862	H1-hESC	embryonic stem cell:	n/a	n/a
28	JUND	chr12:31079056-31079520	H1-hESC	embryonic stem cell:	n/a	chr12:31079339-31079348
29	MAX	chr12:31079777-31080424	SK-N-SH	brain:	n/a	n/a
30	MAX	chr12:31079101-31080426	H1-hESC	embryonic stem cell:	n/a	chr12:31079154-31079164
31	MAX	chr12:31079118-31079641	SK-N-SH	brain:	n/a	chr12:31079154-31079164
32	MAX	chr12:31079099-31079576	SK-N-SH	brain:	n/a	chr12:31079154-31079164
33	MAX	chr12:31079172-31079572	H1-hESC	embryonic stem cell:	n/a	n/a
34	MAX	chr12:31079260-31079599	HepG2	liver:	n/a	n/a
35	MAX	chr12:31079074-31080355	H1-hESC	embryonic stem cell:	n/a	chr12:31079154-31079164
36	MAX	chr12:31079847-31080443	H1-hESC	embryonic stem cell:	n/a	n/a
37	MAX	chr12:31079219-31079709	HepG2	liver:	n/a	n/a
38	MXI1	chr12:31078649-31082379	SK-N-SH	brain:	n/a	chr12:31081271-31081286 chr12:31079353-31079368
39	MXI1	chr12:31078809-31079564	H1-hESC	embryonic stem cell:	n/a	chr12:31079353-31079368
40	MXI1	chr12:31079119-31079802	IMR90	lung:	n/a	chr12:31079353-31079368
41	MYC	chr12:31079993-31080159	H1-hESC	embryonic stem cell:	n/a	n/a
42	MYC	chr12:31078979-31079572	H1-hESC	embryonic stem cell:	n/a	chr12:31079154-31079164
43	POLR2A	chr12:31079198-31079556	SK-N-SH	brain:	n/a	n/a
44	POLR2A	chr12:31079388-31079757	HUVEC	blood vessel:	n/a	n/a
45	POLR2A	chr12:31078506-31080634	SK-N-MC	brain:	n/a	n/a
46	POLR2A	chr12:31080077-31080266	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr12:31078945-31080180	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr12:31079814-31080050	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr12:31079233-31079674	HUVEC	blood vessel:	n/a	n/a
50	POLR2A	chr12:31080198-31080342	H1-hESC	embryonic stem cell:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31078979-31079029	SAEC	small airway:	n/a
2	chr12:31078979-31079029	SAEC	small airway:	n/a
3	chr12:31080052-31080102	AG04450	lung:	fetal
4	chr12:31079406-31079456	ovcar-3	ovarian:	n/a
5	chr12:31078979-31079029	HPAEpiC	pulmonary alveolar:	n/a
6	chr12:31079406-31079456	NHBE	bronchial:	n/a
7	chr12:31079406-31079456	PFSK-1	brain:	n/a
8	chr12:31078979-31079029	PANC-1	pancreas:	n/a
9	chr12:31079406-31079456	HCM	heart:	n/a
10	chr12:31079406-31079456	AG04450	lung:	fetal
11	chr12:31079694-31079744	GM12892	blood:	n/a
12	chr12:31079406-31079456	HCT-116	colon:	n/a
13	chr12:31079406-31079456	AoSMC	blood vessel:	n/a
14	chr12:31078979-31079029	ProgFib	skin:	n/a
15	chr12:31079406-31079456	GM12878	blood:	n/a
16	chr12:31079406-31079456	CMK	blood:	n/a
17	chr12:31078979-31079029	K562	blood:	n/a
18	chr12:31078979-31079029	NH-A	brain:	n/a
19	chr12:31078979-31079029	AG04449	skin:	fetal
20	chr12:31079406-31079456	IMR90	lung:	fetal
21	chr12:31078790-31078840	LNCaP	prostate:	n/a
22	chr12:31079406-31079456	HepG2	liver:	n/a
23	chr12:31078790-31078840	SK-N-MC	brain:	n/a
24	chr12:31080052-31080102	HMEC	breast:	n/a
25	chr12:31078979-31079029	GM12891	blood:	n/a
26	chr12:31079406-31079456	HL-60	blood:	n/a
27	chr12:31079694-31079744	BE2_C	brain:	n/a
28	chr12:31078979-31079029	Hepatocyte	liver:	n/a
29	chr12:31078979-31079029	AG10803	skin:	n/a
30	chr12:31078979-31079029	PrEC	prostate:	n/a
31	chr12:31079694-31079744	HL-60	blood:	n/a
32	chr12:31078979-31079029	HRCEpiC	kidney:	n/a
33	chr12:31079583-31079633	SK-N-SH_RA	brain:	n/a
34	chr12:31078979-31079029	HCM	heart:	n/a
35	chr12:31079406-31079456	NH-A	brain:	n/a
36	chr12:31079694-31079744	ECC-1	luminal epithelium:	n/a
37	chr12:31078979-31079029	SK-N-SH	brain:	n/a
38	chr12:31080052-31080102	AG09309	skin:	n/a
39	chr12:31079406-31079456	AG09309	skin:	n/a
40	chr12:31078790-31078840	AG10803	skin:	n/a
41	chr12:31079583-31079633	SK-N-SH	brain:	n/a
42	chr12:31079583-31079633	BJ	skin:	n/a
43	chr12:31078790-31078840	HIPEpiC	eye:	n/a
44	chr12:31079583-31079633	HRCEpiC	kidney:	n/a
45	chr12:31078790-31078840	MCF-7	breast:	n/a
46	chr12:31078979-31079029	AG09319	gingival:	n/a
47	chr12:31080052-31080102	HRCEpiC	kidney:	n/a
48	chr12:31079583-31079633	GM12892	blood:	n/a
49	chr12:31080052-31080102	H1-hESC	embryonic stem cell:	embryo
50	chr12:31080052-31080102	MCF-7	breast:	n/a

No data

Variant related genes	Relation type
TSPAN11	TF binding region
TSPAN11	CpG island

Extended variants
information (count: 75 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:75 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530166320	chr12:31078691-31078692	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs7966761	chr12:31078704-31078705	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
3	rs528592102	chr12:31078714-31078715	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs570122315	chr12:31078731-31078732	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs373832791	chr12:31078745-31078746	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs530930080	chr12:31078747-31078748	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs529058318	chr12:31078802-31078803	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs552601937	chr12:31078812-31078813	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs145308498	chr12:31078881-31078882	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs191418057	chr12:31078886-31078887	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs149196621	chr12:31078889-31078890	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs74086309	chr12:31078925-31078926	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs183626730	chr12:31078970-31078971	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs143368900	chr12:31078979-31078980	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs201659614	chr12:31078989-31078990	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs34766904	chr12:31079005-31079006	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs540662372	chr12:31079046-31079047	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs187185584	chr12:31079070-31079071	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs545440231	chr12:31079260-31079261	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs557322152	chr12:31079293-31079294	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs577153132	chr12:31079315-31079316	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs541690336	chr12:31079346-31079347	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs376968094	chr12:31079347-31079348	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs530325756	chr12:31079355-31079356	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs373347176	chr12:31079356-31079357	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs565118942	chr12:31079362-31079363	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs75049326	chr12:31079369-31079370	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs547553287	chr12:31079384-31079385	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs531013967	chr12:31079387-31079388	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs191590777	chr12:31079399-31079400	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs375384121	chr12:31079413-31079414	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs565661097	chr12:31079414-31079415	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs182316817	chr12:31079485-31079486	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs546891367	chr12:31079486-31079487	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs7305930	chr12:31079518-31079519	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs535643613	chr12:31079538-31079539	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs888563	chr12:31079567-31079568	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs878161	chr12:31079598-31079599	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs878162	chr12:31079669-31079670	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs557360798	chr12:31079707-31079708	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs576420076	chr12:31079732-31079733	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs572818850	chr12:31079758-31079759	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs533512942	chr12:31079775-31079776	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs369098633	chr12:31079798-31079799	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs112653220	chr12:31079808-31079809	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs553631216	chr12:31079823-31079824	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs575028689	chr12:31079884-31079885	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs375365156	chr12:31079908-31079909	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542449510	chr12:31079921-31079922	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563853738	chr12:31079928-31079929	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
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
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31076400-31079000	Weak transcription	Right Atrium	heart
2	chr12:31076600-31078800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr12:31077800-31079000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:31077800-31079000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr12:31078000-31079000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:31078200-31079000	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr12:31078400-31078800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr12:31078400-31078800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
9	chr12:31078400-31079000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr12:31078400-31079000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
11	chr12:31078400-31079200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
12	chr12:31078400-31080000	Enhancers	Fetal Heart	heart
13	chr12:31078600-31078800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
14	chr12:31078600-31078800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
15	chr12:31078600-31078800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr12:31078600-31078800	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr12:31078600-31078800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
18	chr12:31078600-31078800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
19	chr12:31078600-31078800	Enhancers	Brain Cingulate Gyrus	brain
20	chr12:31078600-31078800	Enhancers	Brain Germinal Matrix	brain
21	chr12:31078600-31078800	Enhancers	Fetal Brain Female	brain
22	chr12:31078600-31078800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
23	chr12:31078600-31078800	Bivalent/Poised TSS	Hela-S3	cervix
24	chr12:31078600-31079000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:31078600-31079000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr12:31078600-31079000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:31078600-31079000	Bivalent Enhancer	Brain Anterior Caudate	brain
28	chr12:31078600-31079000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr12:31078600-31079000	Bivalent Enhancer	Fetal Stomach	stomach
30	chr12:31078600-31079200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr12:31078600-31079200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
32	chr12:31078600-31079200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
33	chr12:31078600-31079200	Enhancers	Left Ventricle	heart
34	chr12:31078600-31079200	Enhancers	Lung	lung
35	chr12:31078800-31079000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
36	chr12:31078800-31079000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
37	chr12:31078800-31079000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
38	chr12:31078800-31079000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr12:31078800-31079000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr12:31078800-31079000	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr12:31078800-31079000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr12:31078800-31079000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr12:31078800-31079000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr12:31078800-31079000	Bivalent Enhancer	Adipose Nuclei	Adipose
45	chr12:31078800-31079000	Enhancers	Brain Angular Gyrus	brain
46	chr12:31078800-31079000	Enhancers	Brain Hippocampus Middle	brain
47	chr12:31078800-31079000	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
48	chr12:31078800-31079000	Enhancers	Brain Substantia Nigra	brain
49	chr12:31078800-31079000	Bivalent Enhancer	Colonic Mucosa	Colon
50	chr12:31078800-31079000	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum

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