Variant report

Variant	nsv515702
Chromosome Location	chr2:99827733-99922967
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	ARID3A	chr2:99895164-99895764	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:99834757-99834783	K562	blood:	n/a	n/a
3	ARID3A	chr2:99870939-99870988	K562	blood:	n/a	n/a
4	BATF	chr2:99856972-99857225	GM12878	blood:	n/a	n/a
5	BATF	chr2:99856950-99857204	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:99854703-99854753	K562	blood:	n/a	n/a
7	BHLHE40	chr2:99895235-99895694	HepG2	liver:	n/a	n/a
8	BHLHE40	chr2:99856952-99857274	GM12878	blood:	n/a	n/a
9	BRCA1	chr2:99897017-99897190	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr2:99887282-99887749	K562	blood:	n/a	n/a
11	CBX3	chr2:99887235-99887673	K562	blood:	n/a	n/a
12	CEBPB	chr2:99898969-99899023	K562	blood:	n/a	n/a
13	CEBPB	chr2:99867010-99867383	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:99895106-99895826	Hela-S3	cervix:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
15	CEBPB	chr2:99895140-99895648	MCF-7	breast:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
16	CEBPB	chr2:99896815-99897096	A549	lung:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
17	CEBPB	chr2:99873103-99873596	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr2:99896759-99897060	MCF-7	breast:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
19	CEBPB	chr2:99867010-99867376	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr2:99895163-99895672	MCF-7	breast:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
21	CEBPB	chr2:99895210-99895580	A549	lung:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
22	CEBPB	chr2:99896793-99897128	HepG2	liver:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
23	CEBPB	chr2:99895245-99895503	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
24	CEBPB	chr2:99895309-99895544	K562	blood:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
25	CEBPB	chr2:99867094-99867402	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr2:99898960-99899066	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:99867071-99867369	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr2:99895111-99895596	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
29	CEBPB	chr2:99895144-99895666	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
30	CEBPB	chr2:99895136-99895626	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
31	CEBPB	chr2:99896754-99897198	Hela-S3	cervix:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
32	CEBPB	chr2:99867003-99867374	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:99895160-99895686	IMR90	lung:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
34	CEBPD	chr2:99832595-99832929	K562	blood:	n/a	n/a
35	CHD2	chr2:99895156-99895749	Hela-S3	cervix:	n/a	n/a
36	CREB1	chr2:99867108-99867416	HepG2	liver:	n/a	n/a
37	CTCF	chr2:99915792-99915870	LNCaP	prostate:	n/a	n/a
38	CTCF	chr2:99855860-99856010	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr2:99862149-99862364	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:99855872-99856043	K562	blood:	n/a	n/a
41	CTCF	chr2:99855860-99856010	NHEK	skin:	n/a	n/a
42	CTCF	chr2:99862580-99862730	GM12873	blood:	n/a	n/a
43	CTCF	chr2:99862160-99862310	SAEC	small airway:	n/a	n/a
44	CTCF	chr2:99862560-99862710	HAc	cerebellar:	n/a	n/a
45	CTCF	chr2:99855847-99856039	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr2:99862230-99862379	MCF-7	breast:	n/a	n/a
47	CTCF	chr2:99855880-99856030	HL-60	blood:	n/a	n/a
48	CTCF	chr2:99855880-99856030	GM12873	blood:	n/a	n/a
49	CTCF	chr2:99882856-99882872	LNCaP	prostate:	n/a	n/a
50	CTCF	chr2:99855880-99856030	GM12871	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:99908962-99909012	AG04450	lung:	fetal
2	chr2:99918603-99918653	NT2-D1	testis:	n/a
3	chr2:99908962-99909012	AG09309	skin:	n/a
4	chr2:99918042-99918092	HMEC	breast:	n/a
5	chr2:99867344-99867394	SK-N-SH_RA	brain:	n/a
6	chr2:99871988-99872038	K562	blood:	n/a
7	chr2:99871988-99872038	Hepatocyte	liver:	n/a
8	chr2:99871988-99872038	SK-N-SH	brain:	n/a
9	chr2:99917669-99917719	PrEC	prostate:	n/a
10	chr2:99908962-99909012	GM12892	blood:	n/a
11	chr2:99871270-99871320	ECC-1	luminal epithelium:	n/a
12	chr2:99917669-99917719	IMR90	lung:	fetal
13	chr2:99917669-99917719	HAEpiC	amniotic membrane:	n/a
14	chr2:99871575-99871625	HRE	kidney:	n/a
15	chr2:99871738-99871788	HNPCEpiC	eye:	n/a
16	chr2:99867344-99867394	GM19239	blood:	n/a
17	chr2:99858763-99858813	HEK293	kidney:	embryo
18	chr2:99871988-99872038	RPTEC	kidney:	n/a
19	chr2:99918042-99918092	HRE	kidney:	n/a
20	chr2:99858763-99858813	RPTEC	kidney:	n/a
21	chr2:99917669-99917719	HCM	heart:	n/a
22	chr2:99917669-99917719	AG09319	gingival:	n/a
23	chr2:99858763-99858813	HCF	heart:	n/a
24	chr2:99871988-99872038	GM19239	blood:	n/a
25	chr2:99918603-99918653	Jurkat	blood:	n/a
26	chr2:99908962-99909012	ProgFib	skin:	n/a
27	chr2:99871270-99871320	SK-N-SH_RA	brain:	n/a
28	chr2:99908962-99909012	AG04449	skin:	fetal
29	chr2:99918767-99918817	Hela-S3	cervix:	n/a
30	chr2:99918042-99918092	BE2_C	brain:	n/a
31	chr2:99871988-99872038	IMR90	lung:	fetal
32	chr2:99918042-99918092	ECC-1	luminal epithelium:	n/a
33	chr2:99912152-99912202	ECC-1	luminal epithelium:	n/a
34	chr2:99872119-99872169	GM12878	blood:	n/a
35	chr2:99867344-99867394	MCF-7	breast:	n/a
36	chr2:99871738-99871788	SAEC	small airway:	n/a
37	chr2:99917669-99917719	HMEC	breast:	n/a
38	chr2:99871270-99871320	SK-N-SH	brain:	n/a
39	chr2:99872119-99872169	GM19239	blood:	n/a
40	chr2:99871270-99871320	HNPCEpiC	eye:	n/a
41	chr2:99918767-99918817	AG04449	skin:	fetal
42	chr2:99871988-99872038	U87	brain:	n/a
43	chr2:99918767-99918817	Jurkat	blood:	n/a
44	chr2:99872119-99872169	HCPEpiC	choroid plexus:	n/a
45	chr2:99918767-99918817	PFSK-1	brain:	n/a
46	chr2:99908962-99909012	MCF10A-Er-Src	breast:	n/a
47	chr2:99918603-99918653	HEEpiC	esophagus:	n/a
48	chr2:99918042-99918092	HRPEpiC	eye:	n/a
49	chr2:99871270-99871320	CMK	blood:	n/a
50	chr2:99912152-99912202	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:99906899..99908404-chr2:99910442..99912055,2	K562	blood:
2	chr2:99906899..99908404-chr2:99910442..99912055,2	K562	blood:
3	chr2:99900352..99903264-chr2:99910186..99913049,2	K562	blood:
4	chr2:99853855..99856752-chr2:99861068..99863308,2	K562	blood:
5	chr2:99855888..99858243-chr2:99952048..99955134,3	MCF-7	breast:
6	chr2:99862632..99864910-chr2:99865655..99867519,2	K562	blood:
7	chr2:99905599..99909122-chr2:99945751..99948599,3	MCF-7	breast:
8	chr2:99845973..99846811-chr6:105648996..105649854,2	MCF-7	breast:
9	chr2:99919697..99922118-chr2:99951528..99953553,2	K562	blood:
10	chr2:99918821..99920555-chr2:99920714..99922754,2	MCF-7	breast:
11	chr2:99860434..99863311-chr2:99975532..99977093,2	MCF-7	breast:
12	chr2:99771253..99773056-chr2:99921350..99922897,2	K562	blood:
13	chr2:99826303..99828635-chr2:99951235..99953825,2	K562	blood:
14	chr2:99795164..99797878-chr2:99854234..99856098,2	K562	blood:
15	chr2:99900352..99903264-chr2:99910186..99913049,2	K562	blood:
16	chr2:99895187..99896703-chr2:99951053..99953668,2	MCF-7	breast:
17	chr2:99862632..99864910-chr2:99865655..99867519,2	K562	blood:
18	chr2:99853855..99856752-chr2:99861068..99863308,2	K562	blood:
19	chr2:99861336..99864136-chr2:99868070..99870464,2	K562	blood:
20	chr2:99866201..99868659-chr2:99869387..99872001,2	K562	blood:
21	chr2:99861336..99864136-chr2:99868070..99870464,2	K562	blood:

Variant related genes	Relation type
LYG2	TF binding region
C2orf15	TF binding region
LYG1	TF binding region
LYG2	CpG island
C2orf15	CpG island
LYG1	CpG island
ENSG00000144182	chromatin interactions
ENSG00000158417	chromatin interactions
ENSG00000241962	chromatin interactions
ENSG00000135951	chromatin interactions
ENSG00000185414	chromatin interactions
ENSG00000115514	chromatin interactions
ENSG00000144214	chromatin interactions
ENSG00000273155	chromatin interactions
ENSG00000158411	chromatin interactions
ENSG00000185674	chromatin interactions

Extended variants
information (count: 3314 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:3314 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7586635	chr2:99827733-99827734	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552641888	chr2:99827782-99827783	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs145829863	chr2:99827784-99827785	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs531843422	chr2:99827815-99827816	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs77065378	chr2:99827819-99827820	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs12233087	chr2:99827888-99827889	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs372599903	chr2:99827955-99827956	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs534162610	chr2:99827988-99827989	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs548047233	chr2:99827989-99827990	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs549568130	chr2:99828029-99828030	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs145535968	chr2:99828055-99828056	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs539007348	chr2:99828064-99828065	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs555744228	chr2:99828103-99828104	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs35351367	chr2:99828213-99828214	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs148823181	chr2:99828321-99828322	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs118034993	chr2:99828325-99828326	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs527827988	chr2:99828362-99828363	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs79128134	chr2:99828390-99828391	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs375657576	chr2:99828484-99828485	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs540917415	chr2:99828598-99828599	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs190379028	chr2:99828642-99828643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577866511	chr2:99828663-99828664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192861360	chr2:99828743-99828744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562889759	chr2:99828747-99828748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531804070	chr2:99828759-99828760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542327664	chr2:99828784-99828785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562069707	chr2:99828800-99828801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115204449	chr2:99828805-99828806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7602401	chr2:99828818-99828819	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs571079546	chr2:99828836-99828837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs28789837	chr2:99828862-99828863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533467593	chr2:99828863-99828864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35970068	chr2:99828911-99828912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549332729	chr2:99828980-99828981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547306974	chr2:99828987-99828988	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143461101	chr2:99829047-99829048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10185090	chr2:99829054-99829055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6542874	chr2:99829070-99829071	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs185073967	chr2:99829098-99829099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs151141449	chr2:99829141-99829142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111817216	chr2:99829164-99829165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs56759715	chr2:99829172-99829173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13011370	chr2:99829174-99829175	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372897000	chr2:99829194-99829195	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373671117	chr2:99829199-99829200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs367844378	chr2:99829204-99829205	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371414042	chr2:99829205-99829206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565680265	chr2:99829246-99829247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189546307	chr2:99829247-99829248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539003752	chr2:99829283-99829284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	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
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:577 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99798600-99836400	Weak transcription	Small Intestine	intestine
2	chr2:99803800-99829600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:99807000-99832600	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr2:99814000-99834800	Weak transcription	Gastric	stomach
5	chr2:99814200-99828200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr2:99814200-99832400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr2:99814400-99842200	Weak transcription	Ovary	ovary
8	chr2:99814400-99842800	Weak transcription	Colon Smooth Muscle	Colon
9	chr2:99814800-99840600	Weak transcription	Brain Hippocampus Middle	brain
10	chr2:99815000-99829000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr2:99815000-99834400	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr2:99815000-99836400	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr2:99815000-99840600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr2:99815000-99840800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr2:99815000-99841800	Weak transcription	Pancreas	Pancrea
16	chr2:99815000-99842400	Weak transcription	Fetal Lung	lung
17	chr2:99815200-99830400	Weak transcription	Brain Anterior Caudate	brain
18	chr2:99815200-99833200	Weak transcription	Lung	lung
19	chr2:99815200-99838400	Weak transcription	Adipose Nuclei	Adipose
20	chr2:99815200-99840600	Weak transcription	Aorta	Aorta
21	chr2:99815200-99841800	Weak transcription	Spleen	Spleen
22	chr2:99815200-99842000	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr2:99815200-99842400	Weak transcription	Brain Substantia Nigra	brain
24	chr2:99815400-99834400	Weak transcription	NHEK	skin
25	chr2:99815400-99834600	Weak transcription	Duodenum Mucosa	Duodenum
26	chr2:99815600-99834400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr2:99815600-99834800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr2:99815600-99842000	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr2:99815600-99842200	Weak transcription	Fetal Stomach	stomach
30	chr2:99815600-99843400	Weak transcription	Fetal Brain Female	brain
31	chr2:99818200-99854600	Weak transcription	Left Ventricle	heart
32	chr2:99818400-99830400	Weak transcription	A549	lung
33	chr2:99818400-99836400	Weak transcription	Brain Angular Gyrus	brain
34	chr2:99818600-99842200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:99818800-99843600	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr2:99819000-99843200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr2:99822200-99830000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr2:99823200-99830800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr2:99823400-99829400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr2:99825200-99843200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr2:99825400-99841800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr2:99826200-99827800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:99826400-99834400	Weak transcription	Fetal Intestine Small	intestine
44	chr2:99827400-99828000	Enhancers	HMEC	breast
45	chr2:99827600-99828000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr2:99827600-99828200	Strong transcription	Brain Germinal Matrix	brain
47	chr2:99827600-99828600	Strong transcription	Primary T cells from cord blood	blood
48	chr2:99827600-99832600	Strong transcription	Stomach Smooth Muscle	stomach
49	chr2:99827600-99842800	Weak transcription	Fetal Brain Male	brain
50	chr2:99827800-99828000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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