Variant report

Variant	nsv1045416
Chromosome Location	chr12:38640895-38887087
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1606)
CpG islands
(count:854)
Chromatin interactive
region (count:18)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1606 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:38710113-38710696	HepG2	liver:	n/a	chr12:38710204-38710220 chr12:38710205-38710221
2	ARID3A	chr12:38722213-38722403	K562	blood:	n/a	n/a
3	ARID3A	chr12:38722185-38722490	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:38778647-38778789	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:38710301-38710555	K562	blood:	n/a	n/a
6	ATF1	chr12:38710296-38710661	K562	blood:	n/a	n/a
7	ATF2	chr12:38710293-38710713	GM12878	blood:	n/a	n/a
8	ATF2	chr12:38744101-38745067	GM12878	blood:	n/a	n/a
9	ATF2	chr12:38710159-38710775	GM12878	blood:	n/a	n/a
10	ATF2	chr12:38744225-38745089	GM12878	blood:	n/a	n/a
11	ATF3	chr12:38710223-38710780	A549	lung:	n/a	n/a
12	ATF3	chr12:38710219-38710780	A549	lung:	n/a	n/a
13	BACH1	chr12:38778825-38779049	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr12:38722036-38722207	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr12:38786453-38786734	GM12878	blood:	n/a	chr12:38786626-38786637
16	BATF	chr12:38744388-38744934	GM12878	blood:	n/a	n/a
17	BATF	chr12:38710371-38710641	GM12878	blood:	n/a	n/a
18	BATF	chr12:38710378-38710679	GM12878	blood:	n/a	n/a
19	BATF	chr12:38780253-38780450	GM12878	blood:	n/a	chr12:38780343-38780354
20	BATF	chr12:38744451-38744982	GM12878	blood:	n/a	n/a
21	BCL11A	chr12:38744355-38744996	GM12878	blood:	n/a	n/a
22	BCL11A	chr12:38710258-38710721	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:38744417-38744818	GM12878	blood:	n/a	n/a
24	BCL3	chr12:38744447-38744862	GM12878	blood:	n/a	n/a
25	BCL3	chr12:38710209-38710812	A549	lung:	n/a	n/a
26	BCL3	chr12:38710141-38710775	A549	lung:	n/a	n/a
27	BCLAF1	chr12:38710098-38710795	GM12878	blood:	n/a	n/a
28	BCLAF1	chr12:38744312-38744895	GM12878	blood:	n/a	n/a
29	BCLAF1	chr12:38710117-38710847	GM12878	blood:	n/a	n/a
30	BCLAF1	chr12:38710352-38710785	K562	blood:	n/a	n/a
31	BHLHE40	chr12:38710353-38710663	HepG2	liver:	n/a	n/a
32	BHLHE40	chr12:38710409-38710609	K562	blood:	n/a	n/a
33	BHLHE40	chr12:38722157-38722342	GM12878	blood:	n/a	n/a
34	BHLHE40	chr12:38710156-38710702	GM12878	blood:	n/a	n/a
35	BRCA1	chr12:38709964-38710766	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr12:38710358-38710669	GM12878	blood:	n/a	n/a
37	BRCA1	chr12:38718322-38719076	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr12:38778630-38780749	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr12:38710387-38710653	HepG2	liver:	n/a	n/a
40	BRCA1	chr12:38710312-38710651	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr12:38786266-38787092	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr12:38794070-38794085	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr12:38784805-38785325	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr12:38710189-38710797	HCT-116	colon:	n/a	n/a
45	CBX3	chr12:38676620-38677125	HCT-116	colon:	n/a	n/a
46	CBX3	chr12:38710362-38710671	K562	blood:	n/a	n/a
47	CBX3	chr12:38676688-38677104	HCT-116	colon:	n/a	n/a
48	CBX3	chr12:38710216-38710780	HCT-116	colon:	n/a	n/a
49	CBX3	chr12:38710156-38710688	K562	blood:	n/a	n/a
50	CEBPB	chr12:38780437-38780637	H1-hESC	embryonic stem cell:	n/a	chr12:38780528-38780539

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:38710953-38711003	Jurkat	blood:	n/a
2	chr12:38710433-38710483	U87	brain:	n/a
3	chr12:38806793-38806843	PrEC	prostate:	n/a
4	chr12:38710433-38710483	HRPEpiC	eye:	n/a
5	chr12:38710433-38710483	Caco-2	colon:	n/a
6	chr12:38710433-38710483	PANC-1	pancreas:	n/a
7	chr12:38710433-38710483	HNPCEpiC	eye:	n/a
8	chr12:38806793-38806843	Hela-S3	cervix:	n/a
9	chr12:38710953-38711003	LNCaP	prostate:	n/a
10	chr12:38710606-38710656	IMR90	lung:	fetal
11	chr12:38710604-38710654	NB4	blood:	n/a
12	chr12:38710604-38710654	A549	lung:	n/a
13	chr12:38710700-38710750	GM12891	blood:	n/a
14	chr12:38710700-38710750	HRE	kidney:	n/a
15	chr12:38806793-38806843	HRE	kidney:	n/a
16	chr12:38710424-38710474	AG10803	skin:	n/a
17	chr12:38710606-38710656	H1-hESC	embryonic stem cell:	embryo
18	chr12:38710433-38710483	BJ	skin:	n/a
19	chr12:38710953-38711003	GM06990	blood:	n/a
20	chr12:38710433-38710483	H1-hESC	embryonic stem cell:	embryo
21	chr12:38710408-38710458	ovcar-3	ovarian:	n/a
22	chr12:38710452-38710502	GM06990	blood:	n/a
23	chr12:38710433-38710483	MCF10A-Er-Src	breast:	n/a
24	chr12:38710700-38710750	AG09319	gingival:	n/a
25	chr12:38710424-38710474	ECC-1	luminal epithelium:	n/a
26	chr12:38710433-38710483	SK-N-SH_RA	brain:	n/a
27	chr12:38710154-38710204	NH-A	brain:	n/a
28	chr12:38710452-38710502	K562	blood:	n/a
29	chr12:38806793-38806843	AG04450	lung:	fetal
30	chr12:38710408-38710458	AG04449	skin:	fetal
31	chr12:38710504-38710554	ECC-1	luminal epithelium:	n/a
32	chr12:38714149-38714199	HUVEC	blood vessel:	n/a
33	chr12:38710452-38710502	NHDF-neo	bronchial:	n/a
34	chr12:38710408-38710458	NH-A	brain:	n/a
35	chr12:38724551-38724601	U87	brain:	n/a
36	chr12:38710606-38710656	HEK293	kidney:	embryo
37	chr12:38710154-38710204	HIPEpiC	eye:	n/a
38	chr12:38710491-38710541	HRPEpiC	eye:	n/a
39	chr12:38710154-38710204	CMK	blood:	n/a
40	chr12:38710408-38710458	NT2-D1	testis:	n/a
41	chr12:38710433-38710483	NT2-D1	testis:	n/a
42	chr12:38710700-38710750	HCF	heart:	n/a
43	chr12:38710606-38710656	HUVEC	blood vessel:	n/a
44	chr12:38710452-38710502	HepG2	liver:	n/a
45	chr12:38710606-38710656	AG04450	lung:	fetal
46	chr12:38714149-38714199	HL-60	blood:	n/a
47	chr12:38710504-38710554	GM12891	blood:	n/a
48	chr12:38710491-38710541	MCF-7	breast:	n/a
49	chr12:38714149-38714199	AG10803	skin:	n/a
50	chr12:38714149-38714199	HAEpiC	amniotic membrane:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:38721798..38722714-chr12:39305427..39306254,2	MCF-7	breast:
2	chr12:34175001..34175865-chr12:38710413..38711151,3	HCT-116	colon:
3	chr12:38721916..38722780-chr12:39497511..39498068,2	MCF-7	breast:
4	chr12:34241238..34243550-chr12:38853316..38855678,2	MCF-7	breast:
5	chr12:38676913..38678502-chr12:38709612..38711993,2	MCF-7	breast:
6	chr1:186105531..186106141-chr12:38883322..38883955,2	MCF-7	breast:
7	chr12:38637847..38640659-chr12:38643822..38646474,2	K562	blood:
8	chr12:38843134..38845389-chr12:38847279..38849955,2	MCF-7	breast:
9	chr12:38778961..38781578-chr12:38784417..38786236,2	MCF-7	breast:
10	chr12:38845594..38847956-chr12:38851662..38853438,2	K562	blood:
11	chr12:38845594..38847956-chr12:38851662..38853438,2	K562	blood:
12	chr12:38722084..38722866-chr12:39667246..39667987,2	MCF-7	breast:
13	chr12:38778961..38781578-chr12:38784417..38786236,2	MCF-7	breast:
14	chr12:38876753..38877648-chr6:116268599..116269448,2	MCF-7	breast:
15	chr12:38837698..38839402-chr12:38841166..38843830,2	K562	blood:
16	chr12:38764399..38764899-chr18:71815043..71815544,2	Hela-S3	cervix:
17	chr12:38837698..38839402-chr12:38841166..38843830,2	K562	blood:
18	chr12:38843134..38845389-chr12:38847279..38849955,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPNE8-5	chr12:38837923-38838124	l_629_chr12:38821325-38838592_lung
2	lnc-CPNE8-5	chr12:38832098-38832212	l_629_chr12:38821325-38838592_lung
3	lnc-ALG10B-3	chr12:38847317-38847776	NONHSAT027683
4	lnc-CPNE8-5	chr12:38821326-38822703	l_629_chr12:38821325-38838592_lung
5	lnc-CPNE8-5	chr12:38824250-38824373	l_629_chr12:38821325-38838592_lung
6	lnc-ALG10B-3	chr12:38846321-38846419	NONHSAT027683
7	lnc-ALG10B-3	chr12:38836308-38836412	NONHSAT027682
8	lnc-ALG10B-3	chr12:38847317-38847681	NONHSAT027682
9	lnc-CPNE8-5	chr12:38838505-38838592	l_629_chr12:38821325-38838592_lung

No data

Variant related genes	Relation type
ALG10B	TF binding region
ENSG00000253016	TF binding region
ENSG00000266333	TF binding region
ENSG00000256878	TF binding region
ALG10B	CpG island
ENSG00000253016	CpG island
ENSG00000266333	CpG island
ENSG00000256878	CpG island
ENSG00000175548	chromatin interactions
ENSG00000141665	chromatin interactions
ENSG00000139133	chromatin interactions

Extended variants
information (count: 6765 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:6765 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557036699	chr12:38640935-38640936	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs561896119	chr12:38640938-38640939	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs545886159	chr12:38640939-38640940	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs185291155	chr12:38640940-38640941	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs572618987	chr12:38640943-38640944	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs115546967	chr12:38640960-38640961	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs386762258	chr12:38640968-38640969	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs202245316	chr12:38640969-38640970	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs75835325	chr12:38640985-38640986	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs544957020	chr12:38641017-38641018	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs560325204	chr12:38641026-38641027	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs549714075	chr12:38641074-38641075	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs532360190	chr12:38641078-38641079	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs149679938	chr12:38641127-38641128	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs566011765	chr12:38641164-38641165	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs370431145	chr12:38641191-38641192	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs549047237	chr12:38645617-38645618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147559797	chr12:38645636-38645637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560979525	chr12:38645648-38645649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141867311	chr12:38645651-38645652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543681814	chr12:38645656-38645657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539104143	chr12:38645659-38645660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552126172	chr12:38645665-38645666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192438924	chr12:38645668-38645669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534917450	chr12:38645699-38645700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565470712	chr12:38645726-38645727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs117177918	chr12:38645728-38645729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150475760	chr12:38645732-38645733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547691803	chr12:38645733-38645734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536614886	chr12:38645741-38645742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556895331	chr12:38645751-38645752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184475539	chr12:38645758-38645759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375093242	chr12:38645785-38645786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189764768	chr12:38645798-38645799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565186884	chr12:38645837-38645838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12316377	chr12:38645863-38645864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs541337513	chr12:38645883-38645884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561215285	chr12:38645895-38645896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181125968	chr12:38645973-38645974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11182997	chr12:38646055-38646056	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs563689464	chr12:38646065-38646066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559592131	chr12:38646091-38646092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185879585	chr12:38646092-38646093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530055123	chr12:38646102-38646103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565631576	chr12:38646144-38646145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548524354	chr12:38646146-38646147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568392789	chr12:38646159-38646160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537336910	chr12:38646160-38646161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188834858	chr12:38646180-38646181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532954948	chr12:38646183-38646184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	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
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:683 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:38640800-38641200	Active TSS	Fetal Heart	heart
2	chr12:38645600-38663800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:38654800-38655200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:38654800-38655800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
5	chr12:38655200-38655600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr12:38655200-38655600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
7	chr12:38662400-38662800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:38662400-38662800	Active TSS	Breast Myoepithelial Primary Cells	Breast
9	chr12:38663800-38664400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr12:38664400-38673400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:38673400-38674000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:38673800-38674000	Enhancers	HMEC	breast
13	chr12:38674000-38675200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr12:38674200-38675200	Weak transcription	HMEC	breast
15	chr12:38675200-38676800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr12:38675200-38677400	Enhancers	HMEC	breast
17	chr12:38675800-38677000	Enhancers	NHEK	skin
18	chr12:38675800-38677800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr12:38676800-38677200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:38677200-38678000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr12:38677400-38677600	Weak transcription	HMEC	breast
22	chr12:38677600-38678000	Enhancers	HMEC	breast
23	chr12:38678000-38682600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr12:38678000-38682600	Weak transcription	HMEC	breast
25	chr12:38682600-38683600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr12:38682600-38683600	Enhancers	HMEC	breast
27	chr12:38683600-38696200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr12:38688400-38688600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr12:38690000-38690600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr12:38696200-38696600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:38701000-38701200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr12:38709400-38709800	Enhancers	HUVEC	blood vessel
33	chr12:38709400-38710000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr12:38709600-38709800	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr12:38709600-38709800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr12:38709600-38709800	Enhancers	Adipose Nuclei	Adipose
37	chr12:38709600-38709800	Enhancers	Brain Anterior Caudate	brain
38	chr12:38709600-38709800	Enhancers	Brain Hippocampus Middle	brain
39	chr12:38709600-38709800	Enhancers	NHDF-Ad	bronchial
40	chr12:38709600-38710000	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr12:38709600-38710000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr12:38709600-38710000	Enhancers	Dnd41	blood
43	chr12:38709600-38710000	Enhancers	Hela-S3	cervix
44	chr12:38709600-38710800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr12:38709800-38710000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
46	chr12:38709800-38710000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr12:38709800-38710000	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr12:38709800-38710000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr12:38709800-38710000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr12:38709800-38710000	Enhancers	Muscle Satellite Cultured Cells	--

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