Variant report

Variant	nsv469744
Chromosome Location	chr2:111998860-112173634
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1189)
CpG islands
(count:123)
Chromatin interactive
region (count:7)
LncRNA
region (count:46)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1189 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112004323-112004568	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:112078700-112078866	K562	blood:	n/a	n/a
3	ARID3A	chr2:112077982-112078035	K562	blood:	n/a	n/a
4	ARID3A	chr2:112142989-112143245	K562	blood:	n/a	n/a
5	ARID3A	chr2:112165582-112165606	K562	blood:	n/a	n/a
6	ARID3A	chr2:112134733-112134923	HepG2	liver:	n/a	n/a
7	ATF1	chr2:112104247-112104437	K562	blood:	n/a	n/a
8	ATF1	chr2:112139588-112139732	K562	blood:	n/a	n/a
9	ATF1	chr2:112165410-112165614	K562	blood:	n/a	n/a
10	ATF1	chr2:112123600-112123901	K562	blood:	n/a	n/a
11	BACH1	chr2:112143146-112143417	K562	blood:	n/a	n/a
12	BACH1	chr2:112078561-112079019	H1-hESC	embryonic stem cell:	n/a	chr2:112078792-112078806
13	BACH1	chr2:112078641-112078944	K562	blood:	n/a	chr2:112078792-112078806
14	BATF	chr2:112074635-112074933	GM12878	blood:	n/a	chr2:112074773-112074784
15	BATF	chr2:112125609-112126213	GM12878	blood:	n/a	chr2:112125629-112125642
16	BATF	chr2:112074557-112074916	GM12878	blood:	n/a	chr2:112074773-112074784
17	BATF	chr2:112037291-112037501	GM12878	blood:	n/a	n/a
18	BATF	chr2:112125762-112126285	GM12878	blood:	n/a	n/a
19	BATF	chr2:112049833-112050062	GM12878	blood:	n/a	n/a
20	BATF	chr2:112073963-112074275	GM12878	blood:	n/a	n/a
21	BATF	chr2:112029496-112029836	GM12878	blood:	n/a	chr2:112029663-112029674
22	BATF	chr2:112077193-112077517	GM12878	blood:	n/a	n/a
23	BATF	chr2:112072875-112073150	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
24	BATF	chr2:112169777-112169962	GM12878	blood:	n/a	chr2:112169903-112169914
25	BATF	chr2:112049811-112050042	GM12878	blood:	n/a	n/a
26	BATF	chr2:112072847-112073098	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
27	BATF	chr2:112077128-112077551	GM12878	blood:	n/a	n/a
28	BATF	chr2:112158868-112159229	GM12878	blood:	n/a	chr2:112159209-112159219
29	BATF	chr2:112158949-112159184	GM12878	blood:	n/a	n/a
30	BATF	chr2:112029454-112029812	GM12878	blood:	n/a	chr2:112029663-112029674
31	BATF	chr2:112131695-112131857	GM12878	blood:	n/a	n/a
32	BCL11A	chr2:112125918-112126134	GM12878	blood:	n/a	n/a
33	BCL11A	chr2:112125764-112126223	GM12878	blood:	n/a	n/a
34	BCL11A	chr2:112072754-112073092	GM12878	blood:	n/a	chr2:112072837-112072846
35	BCL11A	chr2:112072806-112073106	GM12878	blood:	n/a	chr2:112072837-112072846
36	BCL11A	chr2:112087560-112087812	GM12878	blood:	n/a	n/a
37	BHLHE40	chr2:112165402-112165622	K562	blood:	n/a	n/a
38	BHLHE40	chr2:112050013-112050384	HepG2	liver:	n/a	n/a
39	BHLHE40	chr2:112165461-112165741	HepG2	liver:	n/a	n/a
40	BHLHE40	chr2:112133109-112133309	K562	blood:	n/a	n/a
41	BHLHE40	chr2:112168058-112168310	HepG2	liver:	n/a	n/a
42	BHLHE40	chr2:112078723-112078845	K562	blood:	n/a	n/a
43	BHLHE40	chr2:112004162-112004599	HepG2	liver:	n/a	n/a
44	BRCA1	chr2:112004146-112004370	HepG2	liver:	n/a	n/a
45	CBX3	chr2:112040510-112040835	K562	blood:	n/a	n/a
46	CBX3	chr2:112158181-112158517	K562	blood:	n/a	n/a
47	CBX3	chr2:112139460-112139855	K562	blood:	n/a	n/a
48	CBX3	chr2:112078409-112078978	K562	blood:	n/a	n/a
49	CBX3	chr2:112116534-112117202	K562	blood:	n/a	n/a
50	CBX3	chr2:112116542-112117069	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112124380-112124430	T-47D	breast:	n/a
2	chr2:112124380-112124430	T-47D	breast:	n/a
3	chr2:112124380-112124430	NH-A	brain:	n/a
4	chr2:112124118-112124168	IMR90	lung:	fetal
5	chr2:112124118-112124168	RPTEC	kidney:	n/a
6	chr2:112124380-112124430	Hela-S3	cervix:	n/a
7	chr2:112124118-112124168	HMEC	breast:	n/a
8	chr2:112124118-112124168	GM12891	blood:	n/a
9	chr2:112124118-112124168	SK-N-SH_RA	brain:	n/a
10	chr2:112124118-112124168	GM12878	blood:	n/a
11	chr2:112124380-112124430	HAEpiC	amniotic membrane:	n/a
12	chr2:112124380-112124430	HepG2	liver:	n/a
13	chr2:112124380-112124430	SK-N-MC	brain:	n/a
14	chr2:112124380-112124430	AG04449	skin:	fetal
15	chr2:112124118-112124168	SK-N-MC	brain:	n/a
16	chr2:112124380-112124430	H1-hESC	embryonic stem cell:	embryo
17	chr2:112124380-112124430	HRCEpiC	kidney:	n/a
18	chr2:112124118-112124168	MCF10A-Er-Src	breast:	n/a
19	chr2:112124380-112124430	Jurkat	blood:	n/a
20	chr2:112124380-112124430	MCF10A-Er-Src	breast:	n/a
21	chr2:112124380-112124430	HUVEC	blood vessel:	n/a
22	chr2:112124118-112124168	A549	lung:	n/a
23	chr2:112124118-112124168	GM12892	blood:	n/a
24	chr2:112124380-112124430	AG04450	lung:	fetal
25	chr2:112124118-112124168	BE2_C	brain:	n/a
26	chr2:112124380-112124430	GM12892	blood:	n/a
27	chr2:112124380-112124430	HCF	heart:	n/a
28	chr2:112124380-112124430	Hepatocyte	liver:	n/a
29	chr2:112124118-112124168	SK-N-SH	brain:	n/a
30	chr2:112124380-112124430	RPTEC	kidney:	n/a
31	chr2:112124380-112124430	IMR90	lung:	fetal
32	chr2:112124118-112124168	AG10803	skin:	n/a
33	chr2:112124118-112124168	SKMC	muscle:	n/a
34	chr2:112124118-112124168	HCF	heart:	n/a
35	chr2:112124118-112124168	NT2-D1	testis:	n/a
36	chr2:112124118-112124168	H1-hESC	embryonic stem cell:	embryo
37	chr2:112124118-112124168	K562	blood:	n/a
38	chr2:112124380-112124430	AG10803	skin:	n/a
39	chr2:112124118-112124168	AG09309	skin:	n/a
40	chr2:112124118-112124168	MCF-7	breast:	n/a
41	chr2:112124118-112124168	HRPEpiC	eye:	n/a
42	chr2:112124380-112124430	SKMC	muscle:	n/a
43	chr2:112124118-112124168	BJ	skin:	n/a
44	chr2:112124118-112124168	GM19239	blood:	n/a
45	chr2:112124380-112124430	SK-N-SH	brain:	n/a
46	chr2:112124118-112124168	HUVEC	blood vessel:	n/a
47	chr2:112124380-112124430	Caco-2	colon:	n/a
48	chr2:112124118-112124168	HCM	heart:	n/a
49	chr2:112124118-112124168	Caco-2	colon:	n/a
50	chr2:112124118-112124168	NH-A	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:111996763..111999930-chr2:112002314..112005967,4	K562	blood:
2	chr2:112158086..112161064-chr8:43095226..43096729,2	MCF-7	breast:
3	chr2:111878316..111879893-chr2:112101721..112103928,2	MCF-7	breast:
4	chr2:111970999..111973382-chr2:112004350..112006635,2	MCF-7	breast:
5	chr2:111996763..111999930-chr2:112002314..112005967,4	K562	blood:
6	chr2:111992422..111994041-chr2:111997666..112000118,2	MCF-7	breast:
7	chr2:111879395..111881005-chr2:112073345..112075122,2	MCF-7	breast:

(count:46 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC108463.1-3	chr2:112125064-112125152	NONHSAT073622
2	lnc-AC108463.1-3	chr2:112101638-112101814	NONHSAT073622
3	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
4	lnc-BCL2L11-5	chr2:112085950-112086566	NONHSAT073637
5	lnc-AC108463.1-3	chr2:112005725-112005818	NONHSAT073622
6	lnc-BCL2L11-6	chr2:112060981-112061323	NONHSAT073618
7	lnc-AC108463.1-3	chr2:112005725-112005818	ENSG00000172965.6
8	lnc-AC108463.1-4	chr2:112024445-112025050	ENSG00000270190.1
9	lnc-AC108463.1-3	chr2:112101638-112101675	ENSG00000172965.10
10	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
11	lnc-AC108463.1-3	chr2:112005007-112005135	ENSG00000172965.6
12	lnc-AC108463.1-3	chr2:112004962-112005137	NONHSAT073620
13	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
14	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
15	lnc-AC108463.1-3	chr2:112101789-112101814	NONHSAT073639
16	lnc-AC108463.1-3	chr2:112101668-112101814	ENSG00000172965.6
17	lnc-BCL2L11-2	chr2:112037022-112037457	XLOC_001624
18	lnc-BCL2L11-7	chr2:112141383-112141840	NONHSAT147111
19	lnc-BCL2L11-5	chr2:112081976-112082063	l_1923_chr2:112081839-112086268_testes
20	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
21	lnc-BCL2L11-5	chr2:112081840-112081972	l_1923_chr2:112081839-112086268_testes
22	lnc-AC108463.1-4	chr2:112024419-112025062	NONHSAT073632
23	lnc-AC108463.1-3	chr2:112101638-112101701	NONHSAT073620
24	lnc-BCL2L11-2	chr2:112037444-112037486	XLOC_001624
25	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
26	lnc-AC108463.1-3	chr2:112125088-112125152	NONHSAT073639
27	lnc-AC108463.1-6	chr2:112053206-112053623	NONHSAT073635
28	lnc-AC108463.1-3	chr2:112108185-112108338	ENSG00000172965.6
29	lnc-AC108463.1-3	chr2:112125064-112125102	ENSG00000172965.10
30	lnc-BCL2L11-6	chr2:112080919-112081327	NONHSAT073618
31	lnc-AC108463.1-3	chr2:112005725-112005822	NONHSAT073620
32	lnc-AC108463.1-3	chr2:112124591-112125152	NONHSAT073640
33	lnc-AC108463.1-3	chr2:112033908-112033997	ENSG00000172965.6
34	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
35	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
36	lnc-AC108463.1-3	chr2:112071889-112072139	ENSG00000172965.6
37	lnc-BCL2L11-2	chr2:112043757-112044842	XLOC_001624
38	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
39	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
40	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.10
41	lnc-AC108463.1-3	chr2:112005725-112005818	ENSG00000172965.6
42	lnc-BCL2L11-5	chr2:112085950-112086268	l_1923_chr2:112081839-112086268_testes
43	lnc-BCL2L11-5	chr2:112081889-112082063	NONHSAT073637
44	lnc-BCL2L11-6	chr2:112124594-112124991	NONHSAT073618
45	lnc-BCL2L11-2	chr2:112022860-112023040	XLOC_001624
46	lnc-BCL2L11-7	chr2:112141329-112142569	NONHSAT073641

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4435	chr2:112078638-112078659	MIMAT0018951_1

No data

Variant related genes	Relation type
ENSG00000270190	TF binding region
RPS14P4	TF binding region
MIR4435-1HG	TF binding region
ENSG00000229118	TF binding region
ENSG00000223973	TF binding region
MIR4435-1	TF binding region
ENSG00000270190	CpG island
RPS14P4	CpG island
MIR4435-1HG	CpG island
ENSG00000229118	CpG island
ENSG00000223973	CpG island
MIR4435-1	CpG island
ENSG00000153094	chromatin interactions
ITSN2	miRNA target sites
ASCC3	miRNA target sites
KLHL24	miRNA target sites

Extended variants
information (count: 4450 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:4450 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527499985	chr2:111998938-111998939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189481749	chr2:111998939-111998940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567780010	chr2:111998957-111998958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530193390	chr2:111998988-111998989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1464021	chr2:111998997-111998998	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs569935329	chr2:111999019-111999020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181027547	chr2:111999081-111999082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558987705	chr2:111999094-111999095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575560890	chr2:111999114-111999115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544600912	chr2:111999180-111999181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534902220	chr2:111999183-111999184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554715289	chr2:111999188-111999189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573427226	chr2:111999189-111999190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141504080	chr2:111999226-111999227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549225563	chr2:111999227-111999228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535924559	chr2:111999232-111999233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555778853	chr2:111999255-111999256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575943243	chr2:111999272-111999273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544944556	chr2:111999325-111999326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565045158	chr2:111999326-111999327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185920693	chr2:111999340-111999341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541251822	chr2:111999360-111999361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561041898	chr2:111999384-111999385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139637682	chr2:111999407-111999408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542674223	chr2:111999409-111999410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs71431174	chr2:111999422-111999423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs367837715	chr2:111999471-111999472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143658021	chr2:111999478-111999479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563750867	chr2:111999503-111999504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532410628	chr2:111999513-111999514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147162487	chr2:111999535-111999536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190823874	chr2:111999664-111999665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560313799	chr2:111999665-111999666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528178469	chr2:111999697-111999698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540890134	chr2:111999716-111999717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181892594	chr2:111999749-111999750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371950731	chr2:111999755-111999756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111609924	chr2:111999756-111999757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535987527	chr2:111999757-111999758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186101215	chr2:111999774-111999775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564741784	chr2:111999839-111999840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564879504	chr2:111999846-111999847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560827012	chr2:111999898-111999899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532194025	chr2:111999978-111999979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576047951	chr2:112000027-112000028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs13395957	chr2:112000058-112000059	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs550282194	chr2:112000066-112000067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558498766	chr2:112000097-112000098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200444815	chr2:112000156-112000157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572278939	chr2:112000208-112000209	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Breast cancer	22314128	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:1017 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:111954800-112006800	Weak transcription	HUVEC	blood vessel
2	chr2:111975200-112008200	Weak transcription	Pancreas	Pancrea
3	chr2:111977600-112011400	Weak transcription	A549	lung
4	chr2:111985800-112009600	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr2:111986200-112004400	Weak transcription	Osteobl	bone
6	chr2:111986400-112004000	Weak transcription	NHDF-Ad	bronchial
7	chr2:111990000-112004000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:111993200-112008200	Weak transcription	Aorta	Aorta
9	chr2:111993200-112008200	Weak transcription	Lung	lung
10	chr2:111993600-112004000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr2:111993600-112004000	Weak transcription	Fetal Muscle Leg	muscle
12	chr2:111994000-112006800	Weak transcription	Adipose Nuclei	Adipose
13	chr2:111994000-112009600	Weak transcription	Left Ventricle	heart
14	chr2:111994400-112003800	Weak transcription	HSMMtube	muscle
15	chr2:111994400-112004000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr2:111994400-112004000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr2:111994400-112006600	Weak transcription	Right Ventricle	heart
18	chr2:111994600-112004400	Weak transcription	NHEK	skin
19	chr2:111995200-112004000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr2:111995600-112006200	Weak transcription	Gastric	stomach
21	chr2:111995800-112004000	Weak transcription	K562	blood
22	chr2:111996200-112004200	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr2:111996400-112005200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:111996400-112006600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr2:111996400-112009000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr2:111996600-112004200	Weak transcription	Fetal Muscle Trunk	muscle
27	chr2:111996800-112004000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr2:111997000-112004600	Weak transcription	NH-A	brain
29	chr2:111997000-112005000	Weak transcription	NHLF	lung
30	chr2:111997000-112008200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:111997200-112004000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr2:111997400-112003400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr2:111997600-112004000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr2:111997800-112004000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr2:111998000-112000400	Weak transcription	HSMM	muscle
36	chr2:111998000-112003800	Weak transcription	HepG2	liver
37	chr2:111998000-112004200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr2:111998000-112004400	Weak transcription	Dnd41	blood
39	chr2:112000400-112000800	Strong transcription	HSMM	muscle
40	chr2:112000800-112004000	Weak transcription	HSMM	muscle
41	chr2:112002200-112002600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr2:112002200-112003000	Enhancers	Liver	Liver
43	chr2:112002600-112004000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr2:112002600-112008200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr2:112002800-112004400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr2:112003400-112006600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr2:112003400-112006800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:112003800-112004200	Enhancers	HepG2	liver
49	chr2:112003800-112005600	Genic enhancers	HSMMtube	muscle
50	chr2:112004000-112004400	Enhancers	Fetal Muscle Leg	muscle

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