Variant report

Variant	esv2762645
Chromosome Location	chr2:55892248-55963418
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1087)
CpG islands
(count:915)
Chromatin interactive
region (count:77)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1087 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:55942435-55942557	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:55920973-55921350	K562	blood:	n/a	n/a
3	ARID3A	chr2:55920674-55921347	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:55945346-55945659	HepG2	liver:	n/a	n/a
5	ATF1	chr2:55920842-55921225	K562	blood:	n/a	n/a
6	ATF2	chr2:55920708-55921249	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr2:55920700-55921352	GM12878	blood:	n/a	n/a
8	ATF3	chr2:55920763-55921385	A549	lung:	n/a	n/a
9	ATF3	chr2:55920613-55921267	A549	lung:	n/a	n/a
10	BCL3	chr2:55920529-55921291	A549	lung:	n/a	chr2:55921017-55921026
11	BCL3	chr2:55920594-55921316	A549	lung:	n/a	chr2:55921017-55921026
12	BCL3	chr2:55905107-55905379	GM12878	blood:	n/a	n/a
13	BCLAF1	chr2:55920670-55921264	GM12878	blood:	n/a	chr2:55921017-55921026
14	BCLAF1	chr2:55920680-55921228	GM12878	blood:	n/a	chr2:55921017-55921026
15	BHLHE40	chr2:55932430-55932719	K562	blood:	n/a	n/a
16	BHLHE40	chr2:55945473-55945569	K562	blood:	n/a	n/a
17	BHLHE40	chr2:55920736-55921304	GM12878	blood:	n/a	n/a
18	BHLHE40	chr2:55920705-55921206	K562	blood:	n/a	n/a
19	BHLHE40	chr2:55920674-55921168	HepG2	liver:	n/a	n/a
20	BHLHE40	chr2:55932472-55932647	HepG2	liver:	n/a	n/a
21	BRCA1	chr2:55920863-55921320	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr2:55945378-55945616	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr2:55920797-55921147	HepG2	liver:	n/a	n/a
24	CBX3	chr2:55920791-55921259	K562	blood:	n/a	n/a
25	CBX3	chr2:55920607-55921412	HCT-116	colon:	n/a	n/a
26	CBX3	chr2:55920453-55921347	K562	blood:	n/a	n/a
27	CCNT2	chr2:55920752-55921142	K562	blood:	n/a	n/a
28	CEBPB	chr2:55948912-55949291	IMR90	lung:	n/a	chr2:55949206-55949217
29	CEBPB	chr2:55945360-55945674	K562	blood:	n/a	chr2:55945516-55945529 chr2:55945516-55945527
30	CEBPB	chr2:55926536-55926873	HepG2	liver:	n/a	chr2:55926700-55926711
31	CEBPB	chr2:55948782-55949109	MCF-7	breast:	n/a	n/a
32	CEBPB	chr2:55945423-55945678	MCF-7	breast:	n/a	chr2:55945516-55945529 chr2:55945516-55945527
33	CEBPB	chr2:55926680-55926739	IMR90	lung:	n/a	chr2:55926700-55926711
34	CEBPB	chr2:55922763-55922888	H1-hESC	embryonic stem cell:	n/a	chr2:55922831-55922842
35	CEBPB	chr2:55920755-55921304	IMR90	lung:	n/a	chr2:55920993-55921001
36	CEBPB	chr2:55945370-55945664	A549	lung:	n/a	chr2:55945516-55945529 chr2:55945516-55945527
37	CEBPB	chr2:55920770-55921334	Hela-S3	cervix:	n/a	chr2:55920993-55921001
38	CEBPB	chr2:55922752-55922867	A549	lung:	n/a	chr2:55922831-55922842
39	CEBPB	chr2:55921038-55921179	K562	blood:	n/a	n/a
40	CEBPB	chr2:55920919-55921293	H1-hESC	embryonic stem cell:	n/a	chr2:55920993-55921001
41	CEBPB	chr2:55922691-55922925	K562	blood:	n/a	chr2:55922831-55922842
42	CEBPB	chr2:55899983-55900178	K562	blood:	n/a	chr2:55900036-55900047
43	CEBPB	chr2:55948731-55949160	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr2:55909499-55909628	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:55945351-55945798	H1-hESC	embryonic stem cell:	n/a	chr2:55945516-55945529 chr2:55945516-55945527
46	CEBPB	chr2:55920825-55921289	K562	blood:	n/a	chr2:55920993-55921001
47	CEBPB	chr2:55920783-55921309	A549	lung:	n/a	chr2:55920993-55921001
48	CEBPB	chr2:55922691-55922959	HepG2	liver:	n/a	chr2:55922831-55922842
49	CEBPB	chr2:55926697-55926717	A549	lung:	n/a	chr2:55926700-55926711
50	CEBPB	chr2:55920656-55921443	A549	lung:	n/a	chr2:55920993-55921001

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:55921094-55921144	Hela-S3	cervix:	n/a
2	chr2:55920477-55920527	AG09319	gingival:	n/a
3	chr2:55919983-55920033	GM06990	blood:	n/a
4	chr2:55921061-55921111	AoSMC	blood vessel:	n/a
5	chr2:55919983-55920033	BJ	skin:	n/a
6	chr2:55920781-55920831	NH-A	brain:	n/a
7	chr2:55921072-55921122	U87	brain:	n/a
8	chr2:55921061-55921111	H1-hESC	embryonic stem cell:	embryo
9	chr2:55921125-55921175	HCPEpiC	choroid plexus:	n/a
10	chr2:55921094-55921144	PFSK-1	brain:	n/a
11	chr2:55921061-55921111	AG09309	skin:	n/a
12	chr2:55920613-55920663	AG09309	skin:	n/a
13	chr2:55921061-55921111	ProgFib	skin:	n/a
14	chr2:55921045-55921095	HNPCEpiC	eye:	n/a
15	chr2:55923768-55923818	Hepatocyte	liver:	n/a
16	chr2:55920781-55920831	A549	lung:	n/a
17	chr2:55923768-55923818	HCM	heart:	n/a
18	chr2:55920932-55920982	GM06990	blood:	n/a
19	chr2:55921045-55921095	Hepatocyte	liver:	n/a
20	chr2:55920613-55920663	HPAEpiC	pulmonary alveolar:	n/a
21	chr2:55920613-55920663	K562	blood:	n/a
22	chr2:55923768-55923818	GM12878	blood:	n/a
23	chr2:55920781-55920831	ProgFib	skin:	n/a
24	chr2:55916793-55916843	PANC-1	pancreas:	n/a
25	chr2:55920477-55920527	Hela-S3	cervix:	n/a
26	chr2:55920781-55920831	ovcar-3	ovarian:	n/a
27	chr2:55920564-55920614	MCF-7	breast:	n/a
28	chr2:55920781-55920831	HRCEpiC	kidney:	n/a
29	chr2:55920613-55920663	LNCaP	prostate:	n/a
30	chr2:55923768-55923818	ProgFib	skin:	n/a
31	chr2:55920477-55920527	HRPEpiC	eye:	n/a
32	chr2:55921072-55921122	AG04450	lung:	fetal
33	chr2:55920932-55920982	CMK	blood:	n/a
34	chr2:55916793-55916843	NH-A	brain:	n/a
35	chr2:55920613-55920663	SAEC	small airway:	n/a
36	chr2:55920564-55920614	H1-hESC	embryonic stem cell:	embryo
37	chr2:55920932-55920982	T-47D	breast:	n/a
38	chr2:55920564-55920614	Caco-2	colon:	n/a
39	chr2:55923768-55923818	HepG2	liver:	n/a
40	chr2:55921863-55921913	HUVEC	blood vessel:	n/a
41	chr2:55921064-55921114	BJ	skin:	n/a
42	chr2:55920613-55920663	GM12878	blood:	n/a
43	chr2:55920613-55920663	H1-hESC	embryonic stem cell:	embryo
44	chr2:55921045-55921095	RPTEC	kidney:	n/a
45	chr2:55921064-55921114	MCF-7	breast:	n/a
46	chr2:55921094-55921144	ovcar-3	ovarian:	n/a
47	chr2:55921061-55921111	AG04449	skin:	fetal
48	chr2:55921125-55921175	HepG2	liver:	n/a
49	chr2:55920564-55920614	HepG2	liver:	n/a
50	chr2:55920564-55920614	NH-A	brain:	n/a

(count:77 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:55915025..55917034-chr2:55917366..55919436,2	MCF-7	breast:
2	chr2:55910372..55912674-chr2:55919514..55921035,2	MCF-7	breast:
3	chr2:55844240..55846484-chr2:55936559..55939382,2	MCF-7	breast:
4	chr2:55924095..55926502-chr2:55928603..55930302,2	K562	blood:
5	chr2:55941511..55943436-chr2:55949873..55952751,2	K562	blood:
6	chr2:55911687..55914723-chr2:55917441..55920952,3	K562	blood:
7	chr2:55942470..55944889-chr2:56004945..56007451,2	MCF-7	breast:
8	chr2:55952706..55954305-chr2:55954375..55956858,2	MCF-7	breast:
9	chr2:55910858..55913187-chr2:55918020..55920146,2	K562	blood:
10	chr2:55929391..55931366-chr2:55933067..55934702,2	K562	blood:
11	chr2:55901517..55904388-chr2:55919135..55920931,2	K562	blood:
12	chr2:55908037..55910192-chr2:55913450..55914973,2	K562	blood:
13	chr2:55923895..55927237-chr2:55928589..55931342,3	K562	blood:
14	chr2:55945047..55945916-chr2:56236760..56237988,4	MCF-7	breast:
15	chr2:55920465..55921094-chr7:5569393..5570095,2	Hela-S3	cervix:
16	chr2:55903431..55905646-chr2:55905764..55908923,3	K562	blood:
17	chr2:55907894..55910772-chr2:55917200..55919535,2	K562	blood:
18	chr2:55919171..55920952-chr2:55938967..55941895,2	MCF-7	breast:
19	chr2:55900455..55903347-chr2:55904036..55907328,3	K562	blood:
20	chr2:55917770..55919326-chr2:55919482..55921073,2	MCF-7	breast:
21	chr2:55843167..55845991-chr2:55928985..55931317,2	MCF-7	breast:
22	chr2:55945048..55945967-chr2:56236595..56237551,5	K562	blood:
23	chr2:55939884..55941673-chr2:55943999..55946003,2	K562	blood:
24	chr2:55907894..55910772-chr2:55917200..55919535,2	K562	blood:
25	chr2:55944515..55947437-chr2:56188349..56191143,2	MCF-7	breast:
26	chr2:55900367..55902394-chr2:55919082..55920612,2	MCF-7	breast:
27	chr2:55958747..55960432-chr2:56187012..56189326,2	K562	blood:
28	chr2:55891954..55894358-chr2:55898574..55900895,2	K562	blood:
29	chr2:55941986..55943546-chr2:55946701..55948891,2	MCF-7	breast:
30	chr2:55919171..55920952-chr2:55938967..55941895,2	MCF-7	breast:
31	chr2:55943881..55946260-chr2:56171300..56172831,2	K562	blood:
32	chr2:55841795..55844862-chr2:55919047..55922552,3	K562	blood:
33	chr2:55915025..55917034-chr2:55917366..55919436,2	MCF-7	breast:
34	chr2:55941511..55943436-chr2:55949873..55952751,2	K562	blood:
35	chr2:55929391..55931366-chr2:55933067..55934702,2	K562	blood:
36	chr2:55910858..55913187-chr2:55918020..55920146,2	K562	blood:
37	chr2:55924095..55926502-chr2:55928603..55930302,2	K562	blood:
38	chr2:55915324..55917701-chr2:55918761..55921401,5	K562	blood:
39	chr2:55952706..55954305-chr2:55954375..55956858,2	MCF-7	breast:
40	chr2:55843362..55845607-chr2:55918078..55921710,3	K562	blood:
41	chr2:55904255..55906446-chr2:55915981..55918234,2	K562	blood:
42	chr2:55900455..55903347-chr2:55904036..55907328,3	K562	blood:
43	chr2:55917685..55919319-chr2:55933220..55935207,2	MCF-7	breast:
44	chr2:55939884..55941673-chr2:55943999..55946003,2	K562	blood:
45	chr2:55945011..55946407-chr2:56188187..56189117,5	K562	blood:
46	chr2:55917685..55919319-chr2:55933220..55935207,2	MCF-7	breast:
47	chr2:55843805..55846748-chr2:55896170..55899222,4	MCF-7	breast:
48	chr2:55904255..55906446-chr2:55915981..55918234,2	K562	blood:
49	chr2:55915939..55918877-chr2:55919426..55922860,4	MCF-7	breast:
50	chr2:55921422..55922945-chr2:55929842..55931481,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC104-6	chr2:55927183-55927442	NONHSAT070804

No data

Variant related genes	Relation type
PNPT1	TF binding region
PNPT1	CpG island
ENSG00000075624	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000272606	chromatin interactions
ENSG00000207798	chromatin interactions
ENSG00000138041	chromatin interactions
ENSG00000138035	chromatin interactions

Extended variants
information (count: 3222 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3222 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2586954	chr2:55892261-55892262	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183550779	chr2:55892308-55892309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2627779	chr2:55892356-55892357	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs2586955	chr2:55892378-55892379	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs188728407	chr2:55892434-55892435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs193211578	chr2:55892453-55892454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538190606	chr2:55892510-55892511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577489313	chr2:55892576-55892577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551926554	chr2:55892593-55892594	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559826154	chr2:55892606-55892607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571526256	chr2:55892643-55892644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533606650	chr2:55892651-55892652	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553458314	chr2:55892729-55892730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546441093	chr2:55892733-55892734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143153346	chr2:55892764-55892765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377599280	chr2:55892769-55892770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183435791	chr2:55892807-55892808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188545093	chr2:55892846-55892847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147272618	chr2:55892858-55892859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555929146	chr2:55892864-55892865	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576271501	chr2:55892922-55892923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191744493	chr2:55892923-55892924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183920252	chr2:55892925-55892926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572286715	chr2:55892931-55892932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111825745	chr2:55892940-55892941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560563489	chr2:55893009-55893010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs72930864	chr2:55893017-55893018	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs549342039	chr2:55893144-55893145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562766919	chr2:55893153-55893154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532001463	chr2:55893163-55893164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551801631	chr2:55893186-55893187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188338322	chr2:55893240-55893241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191245653	chr2:55893265-55893266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556304175	chr2:55893273-55893274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184288047	chr2:55893299-55893300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577878261	chr2:55893308-55893309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140794351	chr2:55893321-55893322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572853067	chr2:55893324-55893325	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556103765	chr2:55893334-55893335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs782638	chr2:55893336-55893337	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs144893151	chr2:55893341-55893342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558902044	chr2:55893367-55893368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572415162	chr2:55893452-55893453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551524928	chr2:55893466-55893467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541216925	chr2:55893542-55893543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561100859	chr2:55893590-55893591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111473121	chr2:55893616-55893617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558289237	chr2:55893619-55893620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574056512	chr2:55893621-55893622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566213361	chr2:55893665-55893666	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Mental retardation	19951919	CNVD
Myelofibrosis	22110671	CNVD
Microcephaly	20799320	CNVD
camptodactyly	20799320	CNVD
cognitive delay	20799320	CNVD
prenatal and postnatal growth deficiency	20799320	CNVD
ptosis of eyelids	20799320	CNVD
Maculopathy	20981449	CNVD
2p16.1 microdeletion syndrome	22283845	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Multiple myeloma	16616336	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1295 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55846800-55919800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:55847400-55911000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr2:55858200-55920400	Weak transcription	Fetal Heart	heart
4	chr2:55860400-55905400	Weak transcription	Fetal Brain Male	brain
5	chr2:55864000-55893200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr2:55864400-55919600	Weak transcription	NHLF	lung
7	chr2:55866600-55920000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr2:55870400-55920000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr2:55870600-55892800	Weak transcription	Psoas Muscle	Psoas
10	chr2:55870600-55920000	Weak transcription	Rectal Smooth Muscle	rectum
11	chr2:55870800-55893400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:55870800-55903600	Weak transcription	Gastric	stomach
13	chr2:55870800-55909000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr2:55870800-55920400	Weak transcription	Aorta	Aorta
15	chr2:55871000-55893200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr2:55871000-55893200	Weak transcription	Thymus	Thymus
17	chr2:55871000-55920000	Weak transcription	Spleen	Spleen
18	chr2:55871200-55893400	Weak transcription	Brain Cingulate Gyrus	brain
19	chr2:55871200-55905200	Weak transcription	Brain Angular Gyrus	brain
20	chr2:55871400-55905200	Weak transcription	Fetal Kidney	kidney
21	chr2:55873200-55893200	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr2:55873200-55919800	Weak transcription	Small Intestine	intestine
23	chr2:55873800-55899400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr2:55874800-55920200	Weak transcription	Pancreas	Pancrea
25	chr2:55879000-55896200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr2:55879000-55917600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr2:55879200-55902800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:55879400-55914200	Strong transcription	HUES64 Cell Line	embryonic stem cell
29	chr2:55881200-55913000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr2:55881800-55898000	Weak transcription	NHDF-Ad	bronchial
31	chr2:55882000-55893400	Weak transcription	Right Ventricle	heart
32	chr2:55882000-55893400	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr2:55882200-55909600	Weak transcription	Brain Germinal Matrix	brain
34	chr2:55882400-55892600	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr2:55883000-55892400	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr2:55883000-55892600	Weak transcription	Primary B cells from cord blood	blood
37	chr2:55883000-55893400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr2:55883000-55906800	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr2:55883000-55919800	Weak transcription	HSMMtube	muscle
40	chr2:55883200-55892800	Weak transcription	Colon Smooth Muscle	Colon
41	chr2:55883200-55893200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr2:55883200-55893400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr2:55883200-55906600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr2:55883400-55892600	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr2:55883400-55892800	Weak transcription	Brain Anterior Caudate	brain
46	chr2:55883400-55892800	Weak transcription	NHEK	skin
47	chr2:55883400-55893000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr2:55883400-55893000	Weak transcription	Placenta	Placenta
49	chr2:55883400-55893000	Weak transcription	NH-A	brain
50	chr2:55883400-55893400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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