Variant report

Variant	nsv899021
Chromosome Location	chr12:39989172-40053423
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:734)
CpG islands
(count:793)
Chromatin interactive
region (count:18)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:40019707-40020121	K562	blood:	n/a	n/a
2	ATF1	chr12:40017728-40018001	K562	blood:	n/a	n/a
3	ATF2	chr12:40014910-40015547	GM12878	blood:	n/a	n/a
4	ATF2	chr12:40017642-40018058	GM12878	blood:	n/a	n/a
5	ATF2	chr12:40013016-40014468	GM12878	blood:	n/a	n/a
6	ATF2	chr12:40011528-40012131	GM12878	blood:	n/a	n/a
7	ATF2	chr12:40015033-40015558	GM12878	blood:	n/a	n/a
8	ATF2	chr12:40017634-40018151	GM12878	blood:	n/a	n/a
9	ATF2	chr12:40013030-40014309	GM12878	blood:	n/a	n/a
10	BATF	chr12:40015177-40015564	GM12878	blood:	n/a	chr12:40015361-40015369
11	BATF	chr12:40013610-40014176	GM12878	blood:	n/a	n/a
12	BCL11A	chr12:40013743-40014155	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:40015148-40015466	GM12878	blood:	n/a	n/a
14	BCL11A	chr12:40013691-40014229	GM12878	blood:	n/a	n/a
15	BCL11A	chr12:40015067-40015497	GM12878	blood:	n/a	n/a
16	BCLAF1	chr12:40011639-40012238	GM12878	blood:	n/a	chr12:40011861-40011870
17	BCLAF1	chr12:40014878-40015503	GM12878	blood:	n/a	n/a
18	BCLAF1	chr12:40013103-40014371	GM12878	blood:	n/a	chr12:40013531-40013540
19	BCLAF1	chr12:40015092-40015585	GM12878	blood:	n/a	n/a
20	BCLAF1	chr12:40012903-40014227	GM12878	blood:	n/a	chr12:40013531-40013540
21	BHLHE40	chr12:40013332-40013847	K562	blood:	n/a	n/a
22	BHLHE40	chr12:40011766-40012044	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:40013084-40014481	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:40019763-40020115	K562	blood:	n/a	n/a
25	CBX3	chr12:39999295-39999670	HCT-116	colon:	n/a	n/a
26	CBX3	chr12:40019734-40020137	K562	blood:	n/a	chr12:40019836-40019847
27	CBX3	chr12:40019741-40020095	K562	blood:	n/a	chr12:40019836-40019847
28	CCNT2	chr12:40019858-40020181	K562	blood:	n/a	n/a
29	CCNT2	chr12:40037078-40037214	K562	blood:	n/a	n/a
30	CEBPB	chr12:39999255-40000244	HCT-116	colon:	n/a	n/a
31	CEBPB	chr12:39989729-39990205	HCT-116	colon:	n/a	chr12:39989989-39990006
32	CEBPB	chr12:40032622-40033089	MCF-7	breast:	n/a	chr12:40032834-40032845
33	CEBPB	chr12:40040846-40041116	A549	lung:	n/a	chr12:40040993-40041004 chr12:40040994-40041005
34	CEBPB	chr12:40032663-40033020	H1-hESC	embryonic stem cell:	n/a	chr12:40032834-40032845
35	CEBPB	chr12:40032653-40033033	Hela-S3	cervix:	n/a	chr12:40032834-40032845
36	CEBPB	chr12:40032699-40033055	ECC-1	luminal epithelium:	n/a	chr12:40032834-40032845
37	CEBPB	chr12:40045625-40045736	K562	blood:	n/a	chr12:40045690-40045701
38	CEBPB	chr12:40000501-40000724	A549	lung:	n/a	chr12:40000582-40000591 chr12:40000581-40000592
39	CEBPB	chr12:40032511-40033162	K562	blood:	n/a	chr12:40032834-40032845
40	CEBPB	chr12:40032669-40032993	K562	blood:	n/a	chr12:40032834-40032845
41	CEBPB	chr12:39999300-39999670	HCT-116	colon:	n/a	n/a
42	CEBPB	chr12:40040306-40040529	HepG2	liver:	n/a	chr12:40040390-40040403 chr12:40040391-40040402 chr12:40040390-40040403 chr12:40040390-40040401
43	CEBPB	chr12:40045552-40045833	HepG2	liver:	n/a	chr12:40045690-40045701
44	CEBPB	chr12:40000524-40000727	HepG2	liver:	n/a	chr12:40000582-40000591 chr12:40000581-40000592
45	CEBPB	chr12:40045629-40045769	A549	lung:	n/a	chr12:40045690-40045701
46	CEBPB	chr12:40040823-40041125	HepG2	liver:	n/a	chr12:40040993-40041004 chr12:40040994-40041005
47	CEBPB	chr12:40020393-40020736	K562	blood:	n/a	n/a
48	CEBPB	chr12:39999420-39999681	A549	lung:	n/a	n/a
49	CEBPB	chr12:40032657-40033014	HepG2	liver:	n/a	chr12:40032834-40032845
50	CEBPB	chr12:40010503-40010655	HepG2	liver:	n/a	chr12:40010509-40010520 chr12:40010509-40010522

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:40014132-40014182	ProgFib	skin:	n/a
2	chr12:40013596-40013646	H1-hESC	embryonic stem cell:	embryo
3	chr12:40013961-40014011	Jurkat	blood:	n/a
4	chr12:40019907-40019957	HPAEpiC	pulmonary alveolar:	n/a
5	chr12:40019907-40019957	GM12891	blood:	n/a
6	chr12:40014292-40014342	BE2_C	brain:	n/a
7	chr12:40020000-40020050	HCPEpiC	choroid plexus:	n/a
8	chr12:40019532-40019582	LNCaP	prostate:	n/a
9	chr12:40014132-40014182	HRPEpiC	eye:	n/a
10	chr12:40013961-40014011	HAEpiC	amniotic membrane:	n/a
11	chr12:40013961-40014011	HRPEpiC	eye:	n/a
12	chr12:40019919-40019969	Hepatocyte	liver:	n/a
13	chr12:40020000-40020050	HepG2	liver:	n/a
14	chr12:40014292-40014342	SK-N-SH	brain:	n/a
15	chr12:40019907-40019957	AG04449	skin:	fetal
16	chr12:40014132-40014182	HL-60	blood:	n/a
17	chr12:40019883-40019933	A549	lung:	n/a
18	chr12:40014061-40014111	GM06990	blood:	n/a
19	chr12:40013680-40013730	BJ	skin:	n/a
20	chr12:40013680-40013730	HCF	heart:	n/a
21	chr12:40013596-40013646	GM06990	blood:	n/a
22	chr12:40019768-40019818	Jurkat	blood:	n/a
23	chr12:40014061-40014111	GM12891	blood:	n/a
24	chr12:40019907-40019957	HRE	kidney:	n/a
25	chr12:40019768-40019818	NHBE	bronchial:	n/a
26	chr12:40013680-40013730	GM06990	blood:	n/a
27	chr12:40013961-40014011	Hepatocyte	liver:	n/a
28	chr12:40014292-40014342	AG09319	gingival:	n/a
29	chr12:40013680-40013730	SK-N-MC	brain:	n/a
30	chr12:40019768-40019818	Hela-S3	cervix:	n/a
31	chr12:40014061-40014111	GM12892	blood:	n/a
32	chr12:40019883-40019933	HRCEpiC	kidney:	n/a
33	chr12:40014292-40014342	NB4	blood:	n/a
34	chr12:40014292-40014342	U87	brain:	n/a
35	chr12:40014132-40014182	SAEC	small airway:	n/a
36	chr12:40019907-40019957	SKMC	muscle:	n/a
37	chr12:40013961-40014011	RPTEC	kidney:	n/a
38	chr12:40019883-40019933	MCF-7	breast:	n/a
39	chr12:40019768-40019818	PANC-1	pancreas:	n/a
40	chr12:40013680-40013730	NH-A	brain:	n/a
41	chr12:40014132-40014182	HCT-116	colon:	n/a
42	chr12:40019768-40019818	IMR90	lung:	fetal
43	chr12:40013680-40013730	HUVEC	blood vessel:	n/a
44	chr12:40014292-40014342	LNCaP	prostate:	n/a
45	chr12:40019919-40019969	BJ	skin:	n/a
46	chr12:40020078-40020128	AG09319	gingival:	n/a
47	chr12:40014061-40014111	LNCaP	prostate:	n/a
48	chr12:40019532-40019582	Jurkat	blood:	n/a
49	chr12:40014132-40014182	AG09319	gingival:	n/a
50	chr12:40019532-40019582	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:40010562..40012556-chr12:40014262..40016328,2	K562	blood:
2	chr12:40008067..40010229-chr12:40012504..40015238,3	K562	blood:
3	chr12:40014171..40017168-chr12:40017549..40021409,3	K562	blood:
4	chr12:40011374..40014177-chr12:40021729..40023684,2	MCF-7	breast:
5	chr12:39989700..39991592-chr12:39994179..39996342,2	K562	blood:
6	chr12:40041383..40044331-chr12:40082931..40085850,2	K562	blood:
7	chr1:150532408..150532909-chr12:40008630..40009130,2	Hela-S3	cervix:
8	chr12:40010562..40012556-chr12:40014262..40016328,2	K562	blood:
9	chr12:40015362..40017426-chr12:40020461..40022505,2	MCF-7	breast:
10	chr12:39989700..39991592-chr12:39994179..39996342,2	K562	blood:
11	chr12:39998727..40000314-chr12:40002624..40004346,2	MCF-7	breast:
12	chr12:40012703..40015318-chr12:40031815..40033811,2	K562	blood:
13	chr12:40006374..40007995-chr12:40011197..40013165,2	K562	blood:
14	chr12:40006374..40007995-chr12:40011197..40013165,2	K562	blood:
15	chr12:40015362..40017426-chr12:40020461..40022505,2	MCF-7	breast:
16	chr12:40005732..40008128-chr12:40008934..40010953,2	K562	blood:
17	chr12:39998727..40000314-chr12:40002624..40004346,2	MCF-7	breast:
18	chr12:40005732..40008128-chr12:40008934..40010953,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRK2-2	chr12:40035446-40035663	uc_337_+
2	lnc-ABCD2-3	chr12:40035446-40035663	uc_337_-

No data

Variant related genes	Relation type
C12orf40	TF binding region
ABCD2	TF binding region
C12orf40	CpG island
ABCD2	CpG island
ENSG00000173208	chromatin interactions
ENSG00000180116	chromatin interactions

Extended variants
information (count: 1774 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1774 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11172722	chr12:39989172-39989173	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs145915371	chr12:39989178-39989179	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189669099	chr12:39989179-39989180	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192839880	chr12:39989202-39989203	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561897715	chr12:39989255-39989256	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534994006	chr12:39989392-39989393	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76881880	chr12:39989487-39989488	Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs74088756	chr12:39989620-39989621	Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs185296485	chr12:39989654-39989655	Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374654334	chr12:39989671-39989672	Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188845349	chr12:39989691-39989692	Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552190833	chr12:39989692-39989693	Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533354891	chr12:39989757-39989758	Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570561206	chr12:39989773-39989774	Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182025876	chr12:39989777-39989778	Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549914494	chr12:39989815-39989816	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147609714	chr12:39989835-39989836	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568224842	chr12:39989934-39989935	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs578136913	chr12:39989982-39989983	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535658471	chr12:39990007-39990008	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553758737	chr12:39990041-39990042	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565996851	chr12:39990076-39990077	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539439867	chr12:39990124-39990125	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557777718	chr12:39990164-39990165	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576030268	chr12:39990175-39990176	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552000066	chr12:39990225-39990226	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35107971	chr12:39990244-39990245	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543470760	chr12:39990252-39990253	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74916594	chr12:39990265-39990266	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199512892	chr12:39990279-39990280	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184678517	chr12:39990281-39990282	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541645937	chr12:39990309-39990310	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559787503	chr12:39990385-39990386	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533731267	chr12:39990386-39990387	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545721932	chr12:39990402-39990403	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs367943951	chr12:39990439-39990440	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142740084	chr12:39990445-39990446	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201415379	chr12:39990559-39990560	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150306001	chr12:39990577-39990578	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549081246	chr12:39990599-39990600	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568173777	chr12:39990604-39990605	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs137893023	chr12:39990658-39990659	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567295618	chr12:39990661-39990662	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76612569	chr12:39990684-39990685	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565832754	chr12:39990686-39990687	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34046280	chr12:39990707-39990708	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539672661	chr12:39990761-39990762	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs56751990	chr12:39990848-39990849	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189177583	chr12:39990913-39990914	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569679230	chr12:39990968-39990969	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
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
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
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:825 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:39948800-40000000	Weak transcription	Stomach Smooth Muscle	stomach
2	chr12:39963400-39991600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr12:39963800-40010200	Weak transcription	Left Ventricle	heart
4	chr12:39966600-39993200	Weak transcription	GM12878-XiMat	blood
5	chr12:39966600-39993400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr12:39966800-40009400	Weak transcription	Primary T cells from cord blood	blood
7	chr12:39967800-39993200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr12:39973000-39996000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr12:39980000-39993200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr12:39980200-39993000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr12:39980200-39993000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr12:39980200-39993200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr12:39980200-40006000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr12:39980200-40009200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr12:39981600-39999400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr12:39982800-39991200	Weak transcription	Adipose Nuclei	Adipose
17	chr12:39987400-39991400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr12:39987800-40002000	Strong transcription	Primary T cells fromperipheralblood	blood
19	chr12:39988000-39992800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr12:39988000-39999600	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr12:39988400-39991800	Strong transcription	Primary T helper cells PMA-I stimulated	--
22	chr12:39989000-39989400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr12:39989400-39989800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr12:39989800-39991200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr12:39991200-39991400	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr12:39991200-39991600	Enhancers	Adipose Nuclei	Adipose
27	chr12:39991400-39991600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr12:39991400-39992800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr12:39991600-39992200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr12:39991600-39992400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr12:39991600-39993200	Weak transcription	Adipose Nuclei	Adipose
32	chr12:39991800-39997600	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr12:39992200-40000600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr12:39992400-39993200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr12:39992800-39995000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr12:39992800-39996400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr12:39993000-39994600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr12:39993000-39997800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr12:39993200-39993600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr12:39993200-39993600	Strong transcription	GM12878-XiMat	blood
41	chr12:39993200-39993800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr12:39993200-39993800	Strong transcription	Cortex derived primary cultured neurospheres	brain
43	chr12:39993200-39993800	Enhancers	Adipose Nuclei	Adipose
44	chr12:39993200-39994800	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr12:39993400-39994200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
46	chr12:39993600-39993800	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr12:39993600-39997400	Weak transcription	GM12878-XiMat	blood
48	chr12:39993800-39994200	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr12:39993800-39996600	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr12:39993800-40003400	Weak transcription	Adipose Nuclei	Adipose

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