Variant report

Variant	nsv558149
Chromosome Location	chr12:32004170-32094101
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:882)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:882 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:32013397-32013717	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:32007038-32007368	HepG2	liver:	n/a	n/a
3	ATF1	chr12:32049547-32049913	K562	blood:	n/a	n/a
4	ATF2	chr12:32043462-32043919	GM12878	blood:	n/a	n/a
5	ATF2	chr12:32012425-32013045	GM12878	blood:	n/a	n/a
6	ATF2	chr12:32012430-32012848	GM12878	blood:	n/a	n/a
7	ATF2	chr12:32059435-32060240	GM12878	blood:	n/a	n/a
8	ATF2	chr12:32028192-32028592	GM12878	blood:	n/a	n/a
9	ATF2	chr12:32049229-32050151	GM12878	blood:	n/a	n/a
10	ATF2	chr12:32039867-32040549	GM12878	blood:	n/a	n/a
11	ATF2	chr12:32028105-32028579	GM12878	blood:	n/a	n/a
12	ATF2	chr12:32049321-32050102	GM12878	blood:	n/a	n/a
13	BATF	chr12:32059572-32060170	GM12878	blood:	n/a	n/a
14	BATF	chr12:32049356-32049918	GM12878	blood:	n/a	n/a
15	BATF	chr12:32041880-32042149	GM12878	blood:	n/a	n/a
16	BATF	chr12:32012446-32012948	GM12878	blood:	n/a	chr12:32012663-32012674
17	BATF	chr12:32028347-32028606	GM12878	blood:	n/a	chr12:32028517-32028528
18	BATF	chr12:32049428-32049899	GM12878	blood:	n/a	n/a
19	BATF	chr12:32028298-32028690	GM12878	blood:	n/a	chr12:32028517-32028528
20	BCL11A	chr12:32049507-32049881	GM12878	blood:	n/a	n/a
21	BCL11A	chr12:32040193-32040410	GM12878	blood:	n/a	n/a
22	BCL11A	chr12:32040083-32040458	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:32049416-32049989	GM12878	blood:	n/a	n/a
24	BCL3	chr12:32049369-32049919	GM12878	blood:	n/a	n/a
25	BCL3	chr12:32012394-32012917	GM12878	blood:	n/a	n/a
26	BCLAF1	chr12:32028251-32028607	GM12878	blood:	n/a	n/a
27	BCLAF1	chr12:32049209-32050041	GM12878	blood:	n/a	n/a
28	BCLAF1	chr12:32059642-32060136	GM12878	blood:	n/a	n/a
29	BCLAF1	chr12:32049270-32049928	GM12878	blood:	n/a	n/a
30	BCLAF1	chr12:32039797-32040469	GM12878	blood:	n/a	chr12:32039937-32039946
31	BCLAF1	chr12:32012499-32012999	GM12878	blood:	n/a	n/a
32	BHLHE40	chr12:32050871-32051039	K562	blood:	n/a	n/a
33	BHLHE40	chr12:32049571-32049904	K562	blood:	n/a	n/a
34	BHLHE40	chr12:32043557-32043864	GM12878	blood:	n/a	n/a
35	BHLHE40	chr12:32048716-32048763	GM12878	blood:	n/a	n/a
36	BHLHE40	chr12:32039961-32040391	GM12878	blood:	n/a	n/a
37	BHLHE40	chr12:32049476-32050175	GM12878	blood:	n/a	n/a
38	BHLHE40	chr12:32012628-32013027	GM12878	blood:	n/a	n/a
39	CBX3	chr12:32075340-32075536	K562	blood:	n/a	n/a
40	CBX3	chr12:32075887-32076294	K562	blood:	n/a	n/a
41	CBX3	chr12:32075884-32076289	HCT-116	colon:	n/a	n/a
42	CBX3	chr12:32029552-32030076	K562	blood:	n/a	n/a
43	CBX3	chr12:32059717-32060200	HCT-116	colon:	n/a	n/a
44	CBX3	chr12:32050702-32051189	K562	blood:	n/a	n/a
45	CBX3	chr12:32059772-32060064	K562	blood:	n/a	n/a
46	CBX3	chr12:32045083-32045446	K562	blood:	n/a	n/a
47	CBX3	chr12:32040345-32040748	K562	blood:	n/a	n/a
48	CBX3	chr12:32059753-32060189	HCT-116	colon:	n/a	n/a
49	CBX3	chr12:32075247-32075699	K562	blood:	n/a	n/a
50	CBX3	chr12:32075691-32076415	HCT-116	colon:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:32081573-32081623	HCPEpiC	choroid plexus:	n/a
2	chr12:32081573-32081623	Hepatocyte	liver:	n/a
3	chr12:32081573-32081623	AoSMC	blood vessel:	n/a
4	chr12:32081573-32081623	SKMC	muscle:	n/a
5	chr12:32081573-32081623	NHDF-neo	bronchial:	n/a
6	chr12:32081573-32081623	HL-60	blood:	n/a
7	chr12:32081573-32081623	Caco-2	colon:	n/a
8	chr12:32081573-32081623	HEEpiC	esophagus:	n/a
9	chr12:32081573-32081623	SK-N-MC	brain:	n/a
10	chr12:32081573-32081623	HCF	heart:	n/a
11	chr12:32081573-32081623	GM06990	blood:	n/a
12	chr12:32081573-32081623	NB4	blood:	n/a
13	chr12:32081573-32081623	SK-N-SH_RA	brain:	n/a
14	chr12:32081573-32081623	Jurkat	blood:	n/a
15	chr12:32081573-32081623	HIPEpiC	eye:	n/a
16	chr12:32081573-32081623	ProgFib	skin:	n/a
17	chr12:32081573-32081623	PrEC	prostate:	n/a
18	chr12:32081573-32081623	PFSK-1	brain:	n/a
19	chr12:32081573-32081623	HepG2	liver:	n/a
20	chr12:32081573-32081623	PANC-1	pancreas:	n/a
21	chr12:32081573-32081623	GM12878	blood:	n/a
22	chr12:32081573-32081623	A549	lung:	n/a
23	chr12:32081573-32081623	HRE	kidney:	n/a
24	chr12:32081573-32081623	AG09319	gingival:	n/a
25	chr12:32081573-32081623	HAEpiC	amniotic membrane:	n/a
26	chr12:32081573-32081623	SAEC	small airway:	n/a
27	chr12:32081573-32081623	RPTEC	kidney:	n/a
28	chr12:32081573-32081623	GM12892	blood:	n/a
29	chr12:32081573-32081623	AG04450	lung:	fetal
30	chr12:32081573-32081623	NHBE	bronchial:	n/a
31	chr12:32081573-32081623	GM12891	blood:	n/a
32	chr12:32081573-32081623	BE2_C	brain:	n/a
33	chr12:32081573-32081623	AG10803	skin:	n/a
34	chr12:32081573-32081623	HNPCEpiC	eye:	n/a
35	chr12:32081573-32081623	HMEC	breast:	n/a
36	chr12:32081573-32081623	HUVEC	blood vessel:	n/a
37	chr12:32081573-32081623	GM19239	blood:	n/a
38	chr12:32081573-32081623	HRPEpiC	eye:	n/a
39	chr12:32081573-32081623	T-47D	breast:	n/a
40	chr12:32081573-32081623	HPAEpiC	pulmonary alveolar:	n/a
41	chr12:32081573-32081623	MCF-7	breast:	n/a
42	chr12:32081573-32081623	Hela-S3	cervix:	n/a
43	chr12:32081573-32081623	AG04449	skin:	fetal
44	chr12:32081573-32081623	HCT-116	colon:	n/a
45	chr12:32081573-32081623	HEK293	kidney:	embryo
46	chr12:32081573-32081623	K562	blood:	n/a
47	chr12:32081573-32081623	H1-hESC	embryonic stem cell:	embryo
48	chr12:32081573-32081623	BJ	skin:	n/a
49	chr12:32081573-32081623	HRCEpiC	kidney:	n/a
50	chr12:32081573-32081623	HCM	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:32083749..32086378-chr12:32258985..32261277,2	K562	blood:
2	chr12:32081705..32084411-chr12:32112692..32114835,2	K562	blood:
3	chr12:32009885..32011999-chr12:32112315..32115076,2	MCF-7	breast:
4	chr12:32056977..32058627-chr12:32060537..32062486,2	K562	blood:
5	chr12:32004133..32005677-chr12:32006398..32008295,2	K562	blood:
6	chr12:32004133..32005677-chr12:32006398..32008295,2	K562	blood:
7	chr12:32003812..32006453-chr12:32010341..32012776,2	K562	blood:
8	chr12:32003812..32007387-chr12:32010341..32012984,3	K562	blood:
9	chr12:32056977..32058627-chr12:32060537..32062486,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C12orf35-10	chr12:32021031-32021221	NONHSAT027583
2	lnc-H3F3C-6	chr12:32068728-32068779	NONHSAT027589
3	lnc-H3F3C-5	chr12:32005955-32006341	NONHSAT027581
4	lnc-H3F3C-2	chr12:32068298-32068616	NONHSAT027580
5	lnc-H3F3C-2	chr12:32031137-32031852	NONHSAT027580
6	lnc-H3F3C-2	chr12:32030013-32030827	NONHSAT027580
7	lnc-C12orf35-10	chr12:32021854-32021922	NONHSAT027583
8	lnc-H3F3C-2	chr12:32040101-32040159	XLOC_010046
9	lnc-C12orf35-11	chr12:32013251-32013329	NONHSAT027582
10	lnc-H3F3C-2	chr12:32026186-32026629	XLOC_010046
11	lnc-C12orf35-11	chr12:32014294-32015157	NONHSAT027582
12	lnc-H3F3C-6	chr12:32077464-32077521	NONHSAT027589
13	lnc-H3F3C-2	chr12:32057604-32058166	NONHSAT027580
14	lnc-H3F3C-7	chr12:32082065-32082477	NONHSAT027590
15	lnc-H3F3C-6	chr12:32069002-32069098	NONHSAT027589
16	lnc-C12orf35-9	chr12:32046304-32046636	NONHSAT027586

No data

Variant related genes	Relation type
ENSG00000256372	TF binding region
ENSG00000244436	TF binding region
ENSG00000256465	TF binding region
ENSG00000255760	TF binding region
ENSG00000252584	TF binding region
ENSG00000256372	CpG island
ENSG00000244436	CpG island
ENSG00000256465	CpG island
ENSG00000255760	CpG island
ENSG00000252584	CpG island
ENSG00000256372	chromatin interactions
ENSG00000257530	chromatin interactions
ENSG00000174718	chromatin interactions
ENSG00000151746	chromatin interactions

Extended variants
information (count: 3818 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3818 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7980890	chr12:32004170-32004171	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7966081	chr12:32004171-32004172	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs537266126	chr12:32004262-32004263	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs369552210	chr12:32004301-32004302	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs571089481	chr12:32004375-32004376	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs553271680	chr12:32004384-32004385	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs34482099	chr12:32004414-32004415	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs540126203	chr12:32004417-32004418	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs140296942	chr12:32004475-32004476	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs138727236	chr12:32004476-32004477	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs147489601	chr12:32004478-32004479	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs7952965	chr12:32004495-32004496	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs75168248	chr12:32004496-32004497	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs571714428	chr12:32004528-32004529	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs534272883	chr12:32004532-32004533	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs554263876	chr12:32004551-32004552	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs4931574	chr12:32004567-32004568	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs190122857	chr12:32004577-32004578	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs116674349	chr12:32004591-32004592	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs577110166	chr12:32004592-32004593	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs112737528	chr12:32004597-32004598	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs7953104	chr12:32004599-32004600	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs7953105	chr12:32004600-32004601	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs181720107	chr12:32004631-32004632	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs10844028	chr12:32004638-32004639	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs548568923	chr12:32004639-32004640	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs142885462	chr12:32004669-32004670	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs531015346	chr12:32004671-32004672	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs150979512	chr12:32004683-32004684	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs12369204	chr12:32004684-32004685	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs7953213	chr12:32004694-32004695	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs558135659	chr12:32004761-32004762	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs539601828	chr12:32004773-32004774	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs4931575	chr12:32004774-32004775	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs566793078	chr12:32004811-32004812	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs113577581	chr12:32004839-32004840	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs554126827	chr12:32004871-32004872	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs574220428	chr12:32004872-32004873	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs186633420	chr12:32004885-32004886	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs556741170	chr12:32004893-32004894	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs112895245	chr12:32004912-32004913	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs114342325	chr12:32004919-32004920	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs191473838	chr12:32004958-32004959	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs567820919	chr12:32005007-32005008	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs59676255	chr12:32005104-32005105	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs535127349	chr12:32005205-32005206	ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11833816	chr12:32005237-32005238	ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs562063232	chr12:32005241-32005242	ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs112649626	chr12:32005246-32005247	ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530951025	chr12:32005257-32005258	ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	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
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
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	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
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:889 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31996400-32004400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:32001800-32004200	ZNF genes & repeats	Dnd41	blood
3	chr12:32002000-32006400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
4	chr12:32003600-32005200	ZNF genes & repeats	Primary B cells from cord blood	blood
5	chr12:32004800-32005200	Active TSS	Liver	Liver
6	chr12:32005000-32005800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
7	chr12:32005200-32006000	Enhancers	Liver	Liver
8	chr12:32005200-32006200	Strong transcription	Primary B cells from cord blood	blood
9	chr12:32005800-32007400	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr12:32005800-32008400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr12:32005800-32008400	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr12:32006000-32006400	Flanking Active TSS	Liver	Liver
13	chr12:32006000-32007200	Enhancers	Adipose Nuclei	Adipose
14	chr12:32006200-32007000	Enhancers	Brain Substantia Nigra	brain
15	chr12:32006200-32008000	Weak transcription	Primary B cells from cord blood	blood
16	chr12:32006200-32008400	Enhancers	Placenta	Placenta
17	chr12:32006400-32006800	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr12:32006400-32008200	Enhancers	HepG2	liver
19	chr12:32006400-32009400	Enhancers	Liver	Liver
20	chr12:32006800-32008400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr12:32007000-32007600	Enhancers	Hela-S3	cervix
22	chr12:32007200-32007600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr12:32007200-32008200	Weak transcription	Adipose Nuclei	Adipose
24	chr12:32007200-32012000	Weak transcription	Primary B cells from peripheral blood	blood
25	chr12:32008000-32008400	ZNF genes & repeats	Primary B cells from cord blood	blood
26	chr12:32008200-32008400	Enhancers	Adipose Nuclei	Adipose
27	chr12:32008200-32013000	Weak transcription	HepG2	liver
28	chr12:32008400-32008600	Active TSS	Monocytes-CD14+_RO01746	blood
29	chr12:32008400-32009600	Weak transcription	Primary B cells from cord blood	blood
30	chr12:32009000-32009800	ZNF genes & repeats	Thymus	Thymus
31	chr12:32009400-32011000	Weak transcription	Liver	Liver
32	chr12:32009600-32009800	ZNF genes & repeats	Primary B cells from cord blood	blood
33	chr12:32009800-32011000	Weak transcription	Primary B cells from cord blood	blood
34	chr12:32009800-32017200	Weak transcription	Thymus	Thymus
35	chr12:32011000-32011400	Enhancers	Liver	Liver
36	chr12:32011000-32011600	ZNF genes & repeats	Primary B cells from cord blood	blood
37	chr12:32011400-32012800	Weak transcription	Liver	Liver
38	chr12:32011600-32012400	Weak transcription	Primary B cells from cord blood	blood
39	chr12:32012000-32012600	Genic enhancers	Primary B cells from peripheral blood	blood
40	chr12:32012000-32013000	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
41	chr12:32012200-32013400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr12:32012200-32013600	ZNF genes & repeats	GM12878-XiMat	blood
43	chr12:32012200-32013800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
44	chr12:32012400-32013800	Enhancers	Primary B cells from cord blood	blood
45	chr12:32012600-32013200	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr12:32012600-32013600	Enhancers	Primary B cells from peripheral blood	blood
47	chr12:32012800-32013200	Enhancers	Liver	Liver
48	chr12:32013000-32013400	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr12:32013000-32014000	Enhancers	HepG2	liver
50	chr12:32013200-32013600	Flanking Active TSS	Liver	Liver

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