Variant report

Variant	nsv2831
Chromosome Location	chr2:95618109-95662330
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:95622712-95622933	K562	blood:	n/a	n/a
2	BHLHE40	chr2:95652251-95652371	GM12878	blood:	n/a	n/a
3	CEBPB	chr2:95658162-95658466	K562	blood:	n/a	chr2:95658308-95658319
4	CEBPB	chr2:95658156-95658483	IMR90	lung:	n/a	chr2:95658308-95658319
5	CEBPB	chr2:95658180-95658478	A549	lung:	n/a	chr2:95658308-95658319
6	CEBPB	chr2:95658132-95658485	HepG2	liver:	n/a	chr2:95658308-95658319
7	CEBPB	chr2:95629018-95629179	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:95622011-95622035	A549	lung:	n/a	n/a
9	CEBPB	chr2:95658154-95658406	Hela-S3	cervix:	n/a	chr2:95658308-95658319
10	CHD2	chr2:95652249-95652252	GM12878	blood:	n/a	n/a
11	CTCF	chr2:95652251-95652431	MCF-7	breast:	n/a	n/a
12	CTCF	chr2:95652240-95652390	GM12864	blood:	n/a	n/a
13	CTCF	chr2:95622590-95622843	GM19240	blood:	n/a	chr2:95622729-95622738 chr2:95622724-95622740 chr2:95622725-95622738 chr2:95622723-95622741 chr2:95622718-95622739
14	CTCF	chr2:95622680-95622830	GM12874	blood:	n/a	chr2:95622729-95622738 chr2:95622724-95622740 chr2:95622725-95622738 chr2:95622723-95622741 chr2:95622718-95622739
15	CTCF	chr2:95622410-95622429	GM20000	blood:	n/a	n/a
16	CTCF	chr2:95652610-95652683	Lung_OC	lung:	n/a	n/a
17	CTCF	chr2:95639270-95639308	GM20000	blood:	n/a	n/a
18	CTCF	chr2:95622720-95622870	K562	blood:	n/a	chr2:95622729-95622738 chr2:95622724-95622740 chr2:95622725-95622738 chr2:95622723-95622741
19	CTCF	chr2:95652260-95652410	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr2:95622640-95622790	BE2_C	brain:	n/a	chr2:95622729-95622738 chr2:95622724-95622740 chr2:95622725-95622738 chr2:95622723-95622741 chr2:95622718-95622739
21	CTCF	chr2:95652240-95652390	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr2:95623080-95623230	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr2:95626644-95626766	GM19239	blood:	n/a	chr2:95626704-95626717 chr2:95626702-95626720
24	CTCF	chr2:95622593-95622821	A549	lung:	n/a	chr2:95622729-95622738 chr2:95622724-95622740 chr2:95622725-95622738 chr2:95622723-95622741 chr2:95622718-95622739
25	CTCF	chr2:95652143-95652451	MCF-7	breast:	n/a	n/a
26	CTCF	chr2:95622660-95622810	A549	lung:	n/a	chr2:95622729-95622738 chr2:95622724-95622740 chr2:95622725-95622738 chr2:95622723-95622741 chr2:95622718-95622739
27	CTCF	chr2:95653386-95653463	GM12892	blood:	n/a	n/a
28	CTCF	chr2:95621520-95621670	AG09319	gingival:	n/a	n/a
29	CTCF	chr2:95652220-95652370	HMEC	breast:	n/a	n/a
30	CTCF	chr2:95630120-95630270	GM12875	blood:	n/a	n/a
31	CTCF	chr2:95652560-95652710	NB4	blood:	n/a	n/a
32	CTCF	chr2:95652183-95652440	Pancreas_OC	pancreas:	n/a	n/a
33	CTCF	chr2:95652202-95652421	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr2:95622538-95622953	IMR90	lung:	n/a	chr2:95622729-95622738 chr2:95622724-95622740 chr2:95622725-95622738 chr2:95622723-95622741 chr2:95622718-95622739
35	CTCF	chr2:95652175-95652452	GM13977	blood:	n/a	n/a
36	CTCF	chr2:95653400-95653550	GM06990	blood:	n/a	n/a
37	CTCF	chr2:95653381-95653427	GM12891	blood:	n/a	n/a
38	CTCF	chr2:95652192-95652437	A549	lung:	n/a	n/a
39	CTCF	chr2:95652260-95652410	GM12878	blood:	n/a	n/a
40	CTCF	chr2:95659735-95659791	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:95623060-95623210	HVMF	connective:	n/a	n/a
42	CTCF	chr2:95622640-95622790	AG09309	skin:	n/a	chr2:95622729-95622738 chr2:95622724-95622740 chr2:95622725-95622738 chr2:95622723-95622741 chr2:95622718-95622739
43	CTCF	chr2:95652222-95652449	GM19240	blood:	n/a	n/a
44	CTCF	chr2:95652220-95652370	BE2_C	brain:	n/a	n/a
45	CTCF	chr2:95622660-95622810	NHLF	lung:	n/a	chr2:95622729-95622738 chr2:95622724-95622740 chr2:95622725-95622738 chr2:95622723-95622741 chr2:95622718-95622739
46	CTCF	chr2:95652217-95652429	HepG2	liver:	n/a	n/a
47	CTCF	chr2:95622660-95622810	AG04450	lung:	n/a	chr2:95622729-95622738 chr2:95622724-95622740 chr2:95622725-95622738 chr2:95622723-95622741 chr2:95622718-95622739
48	CTCF	chr2:95630108-95630214	MCF-7	breast:	n/a	n/a
49	CTCF	chr2:95622660-95622810	WERI-Rb-1	eye:	n/a	chr2:95622729-95622738 chr2:95622724-95622740 chr2:95622725-95622738 chr2:95622723-95622741 chr2:95622718-95622739
50	CTCF	chr2:95626620-95626770	GM12871	blood:	n/a	chr2:95626704-95626717 chr2:95626702-95626720

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:95659008-95659058	Jurkat	blood:	n/a
2	chr2:95659008-95659058	Jurkat	blood:	n/a
3	chr2:95659008-95659058	NB4	blood:	n/a
4	chr2:95662214-95662264	T-47D	breast:	n/a
5	chr2:95659008-95659058	MCF-7	breast:	n/a
6	chr2:95660093-95660143	AoSMC	blood vessel:	n/a
7	chr2:95659008-95659058	U87	brain:	n/a
8	chr2:95659008-95659058	LNCaP	prostate:	n/a
9	chr2:95662214-95662264	PFSK-1	brain:	n/a
10	chr2:95658954-95659004	HIPEpiC	eye:	n/a
11	chr2:95660093-95660143	HCT-116	colon:	n/a
12	chr2:95659008-95659058	HAEpiC	amniotic membrane:	n/a
13	chr2:95662214-95662264	SAEC	small airway:	n/a
14	chr2:95659008-95659058	HUVEC	blood vessel:	n/a
15	chr2:95659008-95659058	AG04449	skin:	fetal
16	chr2:95662214-95662264	NHDF-neo	bronchial:	n/a
17	chr2:95660093-95660143	ECC-1	luminal epithelium:	n/a
18	chr2:95660093-95660143	HepG2	liver:	n/a
19	chr2:95659008-95659058	PANC-1	pancreas:	n/a
20	chr2:95662214-95662264	NH-A	brain:	n/a
21	chr2:95658954-95659004	HEK293	kidney:	embryo
22	chr2:95660093-95660143	LNCaP	prostate:	n/a
23	chr2:95659008-95659058	NHBE	bronchial:	n/a
24	chr2:95662214-95662264	BJ	skin:	n/a
25	chr2:95662214-95662264	HRE	kidney:	n/a
26	chr2:95658954-95659004	AG09319	gingival:	n/a
27	chr2:95660093-95660143	SK-N-SH_RA	brain:	n/a
28	chr2:95662214-95662264	HCF	heart:	n/a
29	chr2:95658954-95659004	Hela-S3	cervix:	n/a
30	chr2:95658954-95659004	HNPCEpiC	eye:	n/a
31	chr2:95659008-95659058	Caco-2	colon:	n/a
32	chr2:95660093-95660143	K562	blood:	n/a
33	chr2:95658954-95659004	GM19239	blood:	n/a
34	chr2:95662214-95662264	ECC-1	luminal epithelium:	n/a
35	chr2:95660093-95660143	HCF	heart:	n/a
36	chr2:95659008-95659058	GM12892	blood:	n/a
37	chr2:95658954-95659004	PrEC	prostate:	n/a
38	chr2:95662214-95662264	GM12892	blood:	n/a
39	chr2:95662214-95662264	NHBE	bronchial:	n/a
40	chr2:95659008-95659058	HCF	heart:	n/a
41	chr2:95660093-95660143	NHBE	bronchial:	n/a
42	chr2:95660093-95660143	GM12891	blood:	n/a
43	chr2:95658954-95659004	AoSMC	blood vessel:	n/a
44	chr2:95659008-95659058	HRPEpiC	eye:	n/a
45	chr2:95660093-95660143	ovcar-3	ovarian:	n/a
46	chr2:95662214-95662264	K562	blood:	n/a
47	chr2:95659008-95659058	NHDF-neo	bronchial:	n/a
48	chr2:95662214-95662264	Jurkat	blood:	n/a
49	chr2:95662214-95662264	HAEpiC	amniotic membrane:	n/a
50	chr2:95662214-95662264	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:95661631..95663238-chr2:95667762..95669950,2	K562	blood:
2	chr2:95651816..95652782-chr2:95719078..95719828,4	MCF-7	breast:
3	chr2:95424665..95425586-chr2:95622459..95622975,2	MCF-7	breast:
4	chr2:95651914..95652786-chr2:95719057..95719932,5	MCF-7	breast:
5	chr2:95660407..95662839-chr2:95663627..95666532,2	MCF-7	breast:
6	chr2:95648145..95650842-chr2:95696093..95697897,2	MCF-7	breast:
7	chr2:95618477..95620010-chr2:95625385..95627150,2	K562	blood:
8	chr2:95539282..95540717-chr2:95621820..95623346,19	MCF-7	breast:
9	chr2:95651860..95652818-chr2:95707983..95708492,2	MCF-7	breast:
10	chr2:95651308..95654083-chr2:95655355..95658310,2	K562	blood:
11	chr2:95649490..95651105-chr2:95687216..95689663,2	MCF-7	breast:
12	chr2:95652273..95652781-chr2:95718859..95719788,2	K562	blood:
13	chr2:95651873..95654284-chr2:95678219..95680658,2	MCF-7	breast:
14	chr2:95623346..95626792-chr2:95651459..95653827,3	K562	blood:
15	chr2:95656114..95658110-chr2:95658278..95660478,2	MCF-7	breast:
16	chr2:95651850..95652637-chr2:95780825..95781653,3	MCF-7	breast:
17	chr2:95539617..95540636-chr2:95622270..95623579,6	K562	blood:
18	chr2:95623346..95626792-chr2:95651459..95653827,3	K562	blood:
19	chr2:95652032..95652905-chrX:92521732..92522258,2	MCF-7	breast:
20	chr2:95539738..95540291-chr2:95623587..95624478,3	MCF-7	breast:
21	chr2:95539822..95540641-chr2:95622231..95623138,7	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPS5-8	chr2:95627191-95627248	NONHSAT072451
2	lnc-MRPS5-8	chr2:95626792-95627101	NONHSAT072451
3	lnc-MAL-2	chr2:95657625-95657785	NONHSAT072455
4	lnc-MRPS5-9	chr2:95618906-95619243	NONHSAT072448
5	lnc-MRPS5-6	chr2:95640289-95640583	NONHSAT072454
6	lnc-MAL-2	chr2:95659951-95660107	NONHSAT072455
7	lnc-MRPS5-9	chr2:95619323-95619338	NONHSAT072448
8	lnc-MAL-3	chr2:95620586-95620682	NONHSAT072447
9	lnc-MAL-3	chr2:95620957-95621068	NONHSAT072447

Variant related genes	Relation type
ENSG00000231331	TF binding region
ENSG00000233447	TF binding region
ENSG00000233105	TF binding region
ENSG00000232594	TF binding region
ENSG00000224585	TF binding region
ENSG00000235186	TF binding region
ENSG00000231331	CpG island
ENSG00000233447	CpG island
ENSG00000233105	CpG island
ENSG00000232594	CpG island
ENSG00000224585	CpG island
ENSG00000235186	CpG island
ENSG00000231062	chromatin interactions
ENSG00000235186	chromatin interactions
ENSG00000231331	chromatin interactions
ENSG00000242822	chromatin interactions

Extended variants
information (count: 1309 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:1309 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190720299	chr2:95618112-95618113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576780648	chr2:95618116-95618117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531520821	chr2:95618127-95618128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs527273577	chr2:95618137-95618138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548050413	chr2:95618145-95618146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565739649	chr2:95618163-95618164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181484015	chr2:95618165-95618166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539542297	chr2:95618176-95618177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568149144	chr2:95618217-95618218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535160652	chr2:95618223-95618224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547431072	chr2:95618227-95618228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565650873	chr2:95618269-95618270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534524559	chr2:95618284-95618285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189795361	chr2:95618340-95618341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138232826	chr2:95618381-95618382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557707525	chr2:95618419-95618420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143910881	chr2:95618504-95618505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184558270	chr2:95618516-95618517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575964477	chr2:95618519-95618520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574887300	chr2:95618534-95618535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541888096	chr2:95618616-95618617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560137940	chr2:95618657-95618658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371610203	chr2:95618668-95618669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537084669	chr2:95618669-95618670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545729623	chr2:95618670-95618671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555353658	chr2:95618697-95618698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564400062	chr2:95618723-95618724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375268982	chr2:95618724-95618725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531456533	chr2:95618769-95618770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369143919	chr2:95618777-95618778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147309496	chr2:95618779-95618780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369681647	chr2:95618780-95618781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529018422	chr2:95618794-95618795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547493824	chr2:95618802-95618803	Weak transcription Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
35	rs373082032	chr2:95618803-95618804	Weak transcription Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
36	rs188484733	chr2:95618828-95618829	Weak transcription Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
37	rs374651288	chr2:95618870-95618871	Weak transcription Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
38	rs181260670	chr2:95618887-95618888	Weak transcription Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
39	rs537655882	chr2:95618898-95618899	Weak transcription Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
40	rs552093892	chr2:95618908-95618909	Weak transcription Enhancers Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
41	rs186712435	chr2:95618913-95618914	Weak transcription Enhancers Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
42	rs372700941	chr2:95618926-95618927	Weak transcription Enhancers Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
43	rs538117207	chr2:95618930-95618931	Weak transcription Enhancers Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
44	rs190701659	chr2:95618943-95618944	Weak transcription Enhancers Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
45	rs180998175	chr2:95618957-95618958	Weak transcription Enhancers Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
46	rs540819872	chr2:95618971-95618972	Weak transcription Enhancers Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
47	rs568534715	chr2:95619019-95619020	Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
48	rs535583837	chr2:95619033-95619034	Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
49	rs78602871	chr2:95619049-95619050	Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
50	rs113834434	chr2:95619085-95619086	Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:45)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Neuroblastoma	18574593	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:95613600-95620800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:95618800-95619000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr2:95618800-95619000	Flanking Bivalent TSS/Enh	Esophagus	oesophagus
4	chr2:95619000-95619400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
5	chr2:95619000-95619600	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
6	chr2:95619000-95619600	Active TSS	Fetal Thymus	thymus
7	chr2:95621000-95622400	Enhancers	Brain Germinal Matrix	brain
8	chr2:95622400-95622600	Bivalent Enhancer	Brain Angular Gyrus	brain
9	chr2:95623000-95623200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:95624800-95625000	Bivalent Enhancer	Pancreatic Islets	Pancreatic Islet
11	chr2:95624800-95627000	Enhancers	Fetal Lung	lung
12	chr2:95627000-95629200	Weak transcription	Fetal Lung	lung
13	chr2:95629200-95629400	Enhancers	Fetal Lung	lung
14	chr2:95637000-95637400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr2:95637200-95637600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr2:95637200-95638200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:95637400-95637800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr2:95637800-95647600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr2:95642600-95642800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr2:95643400-95643600	Bivalent Enhancer	Fetal Muscle Leg	muscle
21	chr2:95646000-95646200	Enhancers	Esophagus	oesophagus
22	chr2:95646200-95647600	Weak transcription	Esophagus	oesophagus
23	chr2:95647600-95647800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr2:95647600-95648600	Enhancers	Esophagus	oesophagus
25	chr2:95647800-95650600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr2:95648000-95648800	Enhancers	Fetal Thymus	thymus
27	chr2:95648400-95648800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr2:95648400-95648800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr2:95648400-95648800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr2:95648400-95648800	Enhancers	Primary hematopoietic stem cells	blood
31	chr2:95648400-95648800	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr2:95648400-95648800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr2:95648400-95649200	Enhancers	HSMMtube	muscle
34	chr2:95648600-95649200	Weak transcription	Esophagus	oesophagus
35	chr2:95648800-95650600	Weak transcription	Fetal Thymus	thymus
36	chr2:95648800-95651000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr2:95649200-95649400	Enhancers	Esophagus	oesophagus
38	chr2:95649400-95650200	Weak transcription	Esophagus	oesophagus
39	chr2:95650200-95650400	Enhancers	Esophagus	oesophagus
40	chr2:95650400-95650800	Weak transcription	Esophagus	oesophagus
41	chr2:95650600-95651000	Enhancers	Fetal Thymus	thymus
42	chr2:95650600-95651200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr2:95650800-95651600	Enhancers	Esophagus	oesophagus
44	chr2:95651000-95651200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr2:95651000-95651200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr2:95651000-95652200	Weak transcription	Fetal Thymus	thymus
47	chr2:95651200-95660600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr2:95651600-95660600	Weak transcription	Esophagus	oesophagus
49	chr2:95652200-95652400	Enhancers	Fetal Thymus	thymus
50	chr2:95652400-95652800	Weak transcription	Fetal Thymus	thymus

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