Variant report

Variant	nsv1036617
Chromosome Location	chr12:85855093-86010549
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1017)
CpG islands
(count:122)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:85943398-85943797	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:85871019-85871265	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:85862438-85862767	HepG2	liver:	n/a	n/a
4	ATF2	chr12:85920866-85921402	GM12878	blood:	n/a	n/a
5	BACH1	chr12:85862472-85862870	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr12:85929686-85929979	GM12878	blood:	n/a	n/a
7	BATF	chr12:85862502-85862816	GM12878	blood:	n/a	chr12:85862676-85862687
8	BATF	chr12:85862496-85862812	GM12878	blood:	n/a	chr12:85862676-85862687
9	BCL11A	chr12:85903612-85903886	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:85903677-85903924	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:85862437-85862686	HepG2	liver:	n/a	n/a
12	BHLHE40	chr12:85925172-85925543	GM12878	blood:	n/a	n/a
13	BRCA1	chr12:85862456-85862677	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr12:85978809-85979116	HepG2	liver:	n/a	chr12:85978973-85978986 chr12:85978973-85978984 chr12:85978975-85978984 chr12:85978974-85978985 chr12:85978973-85978986 chr12:85978975-85978984 chr12:85978975-85978984 chr12:85978973-85978986 chr12:85978975-85978984
15	CEBPB	chr12:85957585-85957738	Hela-S3	cervix:	n/a	chr12:85957676-85957689 chr12:85957676-85957689 chr12:85957676-85957687 chr12:85957676-85957689 chr12:85957676-85957687
16	CEBPB	chr12:85943405-85943769	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:85895418-85895705	IMR90	lung:	n/a	n/a
18	CEBPB	chr12:85966835-85967062	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr12:85942408-85942794	A549	lung:	n/a	chr12:85942416-85942428
20	CEBPB	chr12:85943425-85943748	A549	lung:	n/a	n/a
21	CEBPB	chr12:85942491-85942784	A549	lung:	n/a	n/a
22	CEBPB	chr12:85942473-85942800	HepG2	liver:	n/a	n/a
23	CEBPB	chr12:85862502-85862738	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr12:86002098-86002319	A549	lung:	n/a	n/a
25	CEBPB	chr12:85942503-85942765	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr12:85948894-85949140	A549	lung:	n/a	chr12:85949046-85949057 chr12:85949018-85949029
27	CEBPB	chr12:85981876-85982197	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr12:85948898-85949146	HepG2	liver:	n/a	chr12:85949046-85949057 chr12:85949018-85949029
29	CEBPB	chr12:86002046-86002376	HepG2	liver:	n/a	n/a
30	CEBPB	chr12:85981944-85982144	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr12:85916987-85917438	Hela-S3	cervix:	n/a	chr12:85917175-85917188
32	CEBPB	chr12:85860458-85861052	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr12:85855499-85855508	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr12:85978878-85979088	A549	lung:	n/a	chr12:85978973-85978986 chr12:85978973-85978984 chr12:85978975-85978984 chr12:85978974-85978985 chr12:85978973-85978986 chr12:85978975-85978984 chr12:85978975-85978984 chr12:85978973-85978986 chr12:85978975-85978984
35	CHD2	chr12:85926171-85926219	GM12878	blood:	n/a	n/a
36	CHD2	chr12:85903634-85903871	GM12878	blood:	n/a	n/a
37	CHD2	chr12:85862495-85862718	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr12:85925018-85925442	GM12878	blood:	n/a	n/a
39	CREB1	chr12:85929762-85930042	GM12878	blood:	n/a	n/a
40	CTCF	chr12:85969600-85969750	GM12868	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
41	CTCF	chr12:85969548-85969782	Pancreas_OC	pancreas:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
42	CTCF	chr12:85862470-85862730	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:85871080-85871230	HPF	lung:	n/a	chr12:85871146-85871167 chr12:85871149-85871157 chr12:85871145-85871161 chr12:85871144-85871162
44	CTCF	chr12:85862520-85862670	BJ	skin:	n/a	n/a
45	CTCF	chr12:85969536-85969732	SK-N-SH_RA	brain:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
46	CTCF	chr12:85870660-85870810	HMEC	breast:	n/a	n/a
47	CTCF	chr12:85871160-85871310	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr12:85862450-85862761	MCF-7	breast:	n/a	n/a
49	CTCF	chr12:85862540-85862690	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr12:85862560-85862710	HUVEC	blood vessel:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:85945089-85945139	RPTEC	kidney:	n/a
2	chr12:85945089-85945139	SK-N-SH_RA	brain:	n/a
3	chr12:85945089-85945139	HRE	kidney:	n/a
4	chr12:85945089-85945139	AG04449	skin:	fetal
5	chr12:85945089-85945139	GM12878	blood:	n/a
6	chr12:85862615-85862665	AoSMC	blood vessel:	n/a
7	chr12:85862615-85862665	HIPEpiC	eye:	n/a
8	chr12:85945089-85945139	HEK293	kidney:	embryo
9	chr12:85862615-85862665	HAEpiC	amniotic membrane:	n/a
10	chr12:85945089-85945139	HUVEC	blood vessel:	n/a
11	chr12:85945089-85945139	PANC-1	pancreas:	n/a
12	chr12:85862615-85862665	Caco-2	colon:	n/a
13	chr12:85862615-85862665	AG04449	skin:	fetal
14	chr12:85945089-85945139	T-47D	breast:	n/a
15	chr12:85862615-85862665	AG09309	skin:	n/a
16	chr12:85945089-85945139	HEEpiC	esophagus:	n/a
17	chr12:85862615-85862665	GM12878	blood:	n/a
18	chr12:85862615-85862665	GM12892	blood:	n/a
19	chr12:85945089-85945139	BJ	skin:	n/a
20	chr12:85945089-85945139	MCF10A-Er-Src	breast:	n/a
21	chr12:85945089-85945139	A549	lung:	n/a
22	chr12:85862615-85862665	GM19239	blood:	n/a
23	chr12:85945089-85945139	NHBE	bronchial:	n/a
24	chr12:85862615-85862665	T-47D	breast:	n/a
25	chr12:85945089-85945139	HL-60	blood:	n/a
26	chr12:85862615-85862665	H1-hESC	embryonic stem cell:	embryo
27	chr12:85862615-85862665	SK-N-SH_RA	brain:	n/a
28	chr12:85862615-85862665	SAEC	small airway:	n/a
29	chr12:85945089-85945139	NHDF-neo	bronchial:	n/a
30	chr12:85945089-85945139	NT2-D1	testis:	n/a
31	chr12:85862615-85862665	HCPEpiC	choroid plexus:	n/a
32	chr12:85862615-85862665	ovcar-3	ovarian:	n/a
33	chr12:85862615-85862665	ProgFib	skin:	n/a
34	chr12:85862615-85862665	PrEC	prostate:	n/a
35	chr12:85945089-85945139	NB4	blood:	n/a
36	chr12:85945089-85945139	IMR90	lung:	fetal
37	chr12:85862615-85862665	NH-A	brain:	n/a
38	chr12:85862615-85862665	SK-N-SH	brain:	n/a
39	chr12:85945089-85945139	HIPEpiC	eye:	n/a
40	chr12:85862615-85862665	SKMC	muscle:	n/a
41	chr12:85862615-85862665	HRCEpiC	kidney:	n/a
42	chr12:85945089-85945139	AG09319	gingival:	n/a
43	chr12:85945089-85945139	ovcar-3	ovarian:	n/a
44	chr12:85862615-85862665	NT2-D1	testis:	n/a
45	chr12:85862615-85862665	ECC-1	luminal epithelium:	n/a
46	chr12:85862615-85862665	HNPCEpiC	eye:	n/a
47	chr12:85945089-85945139	PFSK-1	brain:	n/a
48	chr12:85945089-85945139	HNPCEpiC	eye:	n/a
49	chr12:85862615-85862665	HUVEC	blood vessel:	n/a
50	chr12:85945089-85945139	Caco-2	colon:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:85972231..85974209-chr12:85975781..85977996,2	MCF-7	breast:
2	chr12:85930199..85932678-chr12:85934950..85937006,2	K562	blood:
3	chr12:85972333..85972969-chr12:86260657..86261419,2	MCF-7	breast:
4	chr12:85949711..85951775-chr12:85954587..85956542,2	K562	blood:
5	chr12:85956037..85957820-chr12:85959579..85961160,2	K562	blood:
6	chr12:85956037..85957820-chr12:85959579..85961160,2	K562	blood:
7	chr12:85908005..85909863-chr12:85911172..85913825,2	MCF-7	breast:
8	chr12:85870834..85871570-chr12:86260678..86261344,3	MCF-7	breast:
9	chr12:85968890..85970646-chr12:86260113..86261752,8	MCF-7	breast:
10	chr12:85905968..85908916-chr17:58676509..58679332,2	MCF-7	breast:
11	chr12:85949711..85951775-chr12:85954587..85956542,2	K562	blood:
12	chr12:86002253..86004144-chr12:86006143..86008700,2	MCF-7	breast:
13	chr12:85908005..85909863-chr12:85911172..85913825,2	MCF-7	breast:
14	chr12:85930199..85932678-chr12:85934950..85937006,2	K562	blood:
15	chr12:86002253..86004144-chr12:86006143..86008700,2	MCF-7	breast:
16	chr12:85916869..85918658-chr12:85921402..85924342,2	K562	blood:
17	chr12:85889329..85890032-chr12:85900621..85901187,2	MCF-7	breast:
18	chr12:85916869..85918658-chr12:85921402..85924342,2	K562	blood:
19	chr12:85889329..85890032-chr12:85900621..85901187,2	MCF-7	breast:
20	chr12:85969213..85970141-chr12:86036344..86037184,4	MCF-7	breast:
21	chr12:85870710..85871639-chr12:86266180..86266857,2	MCF-7	breast:
22	chr12:85846574..85849271-chr12:85855607..85858014,2	MCF-7	breast:
23	chr12:85972231..85974209-chr12:85975781..85977996,2	MCF-7	breast:
24	chr12:85861848..85863045-chr12:86266253..86266913,4	MCF-7	breast:
25	chr12:85969245..85970171-chr12:86260729..86261622,3	MCF-7	breast:
26	chr12:85869160..85871446-chr12:85872180..85874528,2	K562	blood:
27	chr12:85862041..85863123-chr12:86313866..86314895,4	MCF-7	breast:
28	chr12:85869160..85871446-chr12:85872180..85874528,2	K562	blood:
29	chr12:86008021..86010789-chr12:86012957..86015625,2	MCF-7	breast:
30	chr12:85940120..85942691-chr12:85944053..85946791,2	MCF-7	breast:
31	chr12:85940120..85942691-chr12:85944053..85946791,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALX1-2	chr12:85988245-85988373	NONHSAT029750

No data

Variant related genes	Relation type
ENSG00000257855	TF binding region
ENSG00000257855	CpG island
ENSG00000170836	chromatin interactions

Extended variants
information (count: 3302 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3302 , 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	rs190777717	chr12:85855114-85855115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs530861118	chr12:85855124-85855125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552129236	chr12:85855132-85855133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371332067	chr12:85855171-85855172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146888904	chr12:85855195-85855196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564285172	chr12:85855226-85855227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546330149	chr12:85855229-85855230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567835798	chr12:85855243-85855244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111297767	chr12:85855337-85855338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536411566	chr12:85855360-85855361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181653336	chr12:85855373-85855374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186278114	chr12:85855411-85855412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12319849	chr12:85855493-85855494	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs11611196	chr12:85855507-85855508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140726416	chr12:85855539-85855540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577126736	chr12:85855554-85855555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549574685	chr12:85855594-85855595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150475117	chr12:85855636-85855637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572067571	chr12:85855723-85855724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568126770	chr12:85855749-85855750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs74112031	chr12:85855804-85855805	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs190673358	chr12:85855887-85855888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181085699	chr12:85855925-85855926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575600258	chr12:85855929-85855930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547780776	chr12:85855936-85855937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564408207	chr12:85855972-85855973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145462184	chr12:85856044-85856045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185781978	chr12:85856103-85856104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368637910	chr12:85856131-85856132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190641560	chr12:85856142-85856143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561428965	chr12:85856151-85856152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148813111	chr12:85856177-85856178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548368310	chr12:85856183-85856184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569958647	chr12:85856245-85856246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182981172	chr12:85856262-85856263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552549889	chr12:85856330-85856331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200947180	chr12:85856357-85856358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201629410	chr12:85856358-85856359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs397821025	chr12:85856360-85856361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372893582	chr12:85856361-85856362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571147171	chr12:85856392-85856393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143519071	chr12:85856415-85856416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376266391	chr12:85856489-85856490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188681120	chr12:85856497-85856498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192489550	chr12:85856582-85856583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558683588	chr12:85856629-85856630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs574965410	chr12:85856679-85856680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs386764913	chr12:85856729-85856730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187246378	chr12:85856730-85856731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570589397	chr12:85856731-85856732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85851400-85859200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr12:85854800-85855400	Enhancers	NHEK	skin
3	chr12:85855000-85855400	Enhancers	HMEC	breast
4	chr12:85855200-85855600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:85855400-85858600	Weak transcription	HMEC	breast
6	chr12:85855400-85858600	Weak transcription	NHEK	skin
7	chr12:85855600-85859800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:85856600-85857400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr12:85856600-85859600	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr12:85856600-85859600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr12:85856800-85857000	Enhancers	Fetal Kidney	kidney
12	chr12:85856800-85857200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr12:85856800-85857200	Enhancers	Primary T cells from cord blood	blood
14	chr12:85856800-85857200	Enhancers	Primary hematopoietic stem cells	blood
15	chr12:85857200-85858200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr12:85857200-85858800	Weak transcription	Fetal Kidney	kidney
17	chr12:85857200-85861200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr12:85857400-85858400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr12:85858200-85860000	Enhancers	Primary hematopoietic stem cells	blood
20	chr12:85858400-85859600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr12:85858600-85859000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr12:85858600-85859000	Enhancers	HSMMtube	muscle
23	chr12:85858600-85859600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr12:85858600-85859600	Enhancers	NH-A	brain
25	chr12:85858600-85860400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr12:85858600-85861400	Enhancers	Muscle Satellite Cultured Cells	--
27	chr12:85858600-85862600	Enhancers	HSMM	muscle
28	chr12:85858600-85862600	Enhancers	NHEK	skin
29	chr12:85858600-85863000	Enhancers	HMEC	breast
30	chr12:85858800-85859200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr12:85858800-85859600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr12:85858800-85860000	Enhancers	Fetal Kidney	kidney
33	chr12:85858800-85860800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr12:85859000-85859200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr12:85859000-85859400	Weak transcription	HSMMtube	muscle
36	chr12:85859000-85859800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr12:85859200-85859400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr12:85859200-85860200	Enhancers	Adipose Nuclei	Adipose
39	chr12:85859200-85860400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr12:85859400-85859600	Enhancers	HSMMtube	muscle
41	chr12:85859400-85859800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr12:85859600-85861800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr12:85859600-85862000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr12:85859600-85862000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr12:85859600-85862200	Weak transcription	HSMMtube	muscle
46	chr12:85859800-85860000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr12:85859800-85861000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr12:85859800-85862400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr12:85860000-85860600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr12:85860000-85862200	Weak transcription	Primary hematopoietic stem cells	blood

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