Variant report

Variant	esv3348872
Chromosome Location	chr12:123192296-123213461
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:445)
CpG islands
(count:488)
Chromatin interactive
region (count:12)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:123201358-123201518	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:123205566-123205898	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:123210672-123210820	K562	blood:	n/a	n/a
4	ATF1	chr12:123210635-123210977	K562	blood:	n/a	n/a
5	ATF2	chr12:123204895-123205418	GM12878	blood:	n/a	n/a
6	ATF2	chr12:123204789-123205408	GM12878	blood:	n/a	n/a
7	ATF2	chr12:123210410-123211094	GM12878	blood:	n/a	n/a
8	ATF2	chr12:123210466-123210885	GM12878	blood:	n/a	n/a
9	ATF2	chr12:123209037-123209549	GM12878	blood:	n/a	n/a
10	ATF2	chr12:123205558-123206155	GM12878	blood:	n/a	n/a
11	ATF2	chr12:123205629-123206088	GM12878	blood:	n/a	n/a
12	BATF	chr12:123205543-123206143	GM12878	blood:	n/a	n/a
13	BATF	chr12:123209199-123209452	GM12878	blood:	n/a	n/a
14	BATF	chr12:123198368-123198752	GM12878	blood:	n/a	n/a
15	BATF	chr12:123205050-123205325	GM12878	blood:	n/a	chr12:123205161-123205169
16	BATF	chr12:123203623-123203925	GM12878	blood:	n/a	n/a
17	BATF	chr12:123203568-123203966	GM12878	blood:	n/a	n/a
18	BATF	chr12:123210498-123210895	GM12878	blood:	n/a	n/a
19	BATF	chr12:123204957-123205419	GM12878	blood:	n/a	chr12:123205161-123205169
20	BATF	chr12:123198415-123198667	GM12878	blood:	n/a	n/a
21	BATF	chr12:123205671-123206135	GM12878	blood:	n/a	n/a
22	BATF	chr12:123210530-123210866	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:123204972-123205414	GM12878	blood:	n/a	n/a
24	BCL11A	chr12:123205656-123206061	GM12878	blood:	n/a	chr12:123205903-123205912 chr12:123205904-123205913
25	BCL11A	chr12:123210605-123210791	GM12878	blood:	n/a	n/a
26	BCL11A	chr12:123198389-123198642	GM12878	blood:	n/a	chr12:123198604-123198613
27	BCL11A	chr12:123210575-123210904	GM12878	blood:	n/a	n/a
28	BCL3	chr12:123205716-123206048	GM12878	blood:	n/a	chr12:123205903-123205912 chr12:123205904-123205913
29	BCL3	chr12:123204901-123205335	GM12878	blood:	n/a	n/a
30	BCLAF1	chr12:123204694-123205409	GM12878	blood:	n/a	n/a
31	BCLAF1	chr12:123210420-123210976	GM12878	blood:	n/a	n/a
32	BCLAF1	chr12:123205600-123206137	GM12878	blood:	n/a	chr12:123205903-123205912 chr12:123205904-123205913
33	BCLAF1	chr12:123209100-123209784	GM12878	blood:	n/a	n/a
34	BHLHE40	chr12:123210534-123210860	GM12878	blood:	n/a	n/a
35	BHLHE40	chr12:123210652-123210840	K562	blood:	n/a	n/a
36	BHLHE40	chr12:123205681-123206131	GM12878	blood:	n/a	n/a
37	CBX3	chr12:123192855-123193151	K562	blood:	n/a	n/a
38	CBX3	chr12:123210454-123211278	HCT-116	colon:	n/a	n/a
39	CCNT2	chr12:123210602-123210819	K562	blood:	n/a	n/a
40	CEBPB	chr12:123204643-123205457	GM12878	blood:	n/a	chr12:123205169-123205182
41	CEBPB	chr12:123201328-123201540	A549	lung:	n/a	n/a
42	CEBPB	chr12:123205513-123206231	GM12878	blood:	n/a	n/a
43	CEBPB	chr12:123192061-123192396	A549	lung:	n/a	chr12:123192205-123192216
44	CEBPB	chr12:123205020-123205301	IMR90	lung:	n/a	chr12:123205169-123205182
45	CEBPB	chr12:123205003-123205333	Hela-S3	cervix:	n/a	chr12:123205169-123205182
46	CEBPB	chr12:123192059-123192377	IMR90	lung:	n/a	chr12:123192205-123192216
47	CEBPB	chr12:123201401-123201532	HepG2	liver:	n/a	n/a
48	CEBPB	chr12:123201306-123201554	HepG2	liver:	n/a	n/a
49	CEBPB	chr12:123201228-123201618	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr12:123194984-123195338	MCF-7	breast:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:123213241-123213291	MCF-7	breast:	n/a
2	chr12:123200533-123200583	PANC-1	pancreas:	n/a
3	chr12:123201372-123201422	HRPEpiC	eye:	n/a
4	chr12:123200533-123200583	NT2-D1	testis:	n/a
5	chr12:123200953-123201003	SAEC	small airway:	n/a
6	chr12:123201372-123201422	SK-N-MC	brain:	n/a
7	chr12:123201189-123201239	HCM	heart:	n/a
8	chr12:123200533-123200583	ECC-1	luminal epithelium:	n/a
9	chr12:123201372-123201422	AoSMC	blood vessel:	n/a
10	chr12:123200953-123201003	HNPCEpiC	eye:	n/a
11	chr12:123200533-123200583	AoSMC	blood vessel:	n/a
12	chr12:123200353-123200403	SAEC	small airway:	n/a
13	chr12:123201189-123201239	NB4	blood:	n/a
14	chr12:123211133-123211183	HPAEpiC	pulmonary alveolar:	n/a
15	chr12:123201189-123201239	LNCaP	prostate:	n/a
16	chr12:123201362-123201412	AG04450	lung:	fetal
17	chr12:123201189-123201239	SKMC	muscle:	n/a
18	chr12:123201362-123201412	NH-A	brain:	n/a
19	chr12:123201362-123201412	Caco-2	colon:	n/a
20	chr12:123201362-123201412	PFSK-1	brain:	n/a
21	chr12:123201372-123201422	ECC-1	luminal epithelium:	n/a
22	chr12:123200353-123200403	Jurkat	blood:	n/a
23	chr12:123201362-123201412	MCF-7	breast:	n/a
24	chr12:123201372-123201422	HIPEpiC	eye:	n/a
25	chr12:123200533-123200583	AG04449	skin:	fetal
26	chr12:123201372-123201422	Hela-S3	cervix:	n/a
27	chr12:123200353-123200403	AG09309	skin:	n/a
28	chr12:123201362-123201412	AG09309	skin:	n/a
29	chr12:123211133-123211183	AoSMC	blood vessel:	n/a
30	chr12:123200353-123200403	H1-hESC	embryonic stem cell:	embryo
31	chr12:123200953-123201003	AoSMC	blood vessel:	n/a
32	chr12:123201189-123201239	HNPCEpiC	eye:	n/a
33	chr12:123200953-123201003	BE2_C	brain:	n/a
34	chr12:123200953-123201003	AG04450	lung:	fetal
35	chr12:123213241-123213291	HMEC	breast:	n/a
36	chr12:123213241-123213291	AG04450	lung:	fetal
37	chr12:123200953-123201003	HL-60	blood:	n/a
38	chr12:123211133-123211183	HRE	kidney:	n/a
39	chr12:123200533-123200583	ovcar-3	ovarian:	n/a
40	chr12:123201372-123201422	PANC-1	pancreas:	n/a
41	chr12:123200953-123201003	SK-N-MC	brain:	n/a
42	chr12:123201362-123201412	HEEpiC	esophagus:	n/a
43	chr12:123200953-123201003	SK-N-SH_RA	brain:	n/a
44	chr12:123200533-123200583	GM12892	blood:	n/a
45	chr12:123200353-123200403	MCF-7	breast:	n/a
46	chr12:123211133-123211183	HEEpiC	esophagus:	n/a
47	chr12:123213241-123213291	Hela-S3	cervix:	n/a
48	chr12:123213241-123213291	SK-N-SH	brain:	n/a
49	chr12:123213241-123213291	HEK293	kidney:	embryo
50	chr12:123213241-123213291	Hepatocyte	liver:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123213106..123215069-chr12:123321149..123322935,2	MCF-7	breast:
2	chr12:123204275..123207099-chr12:123214252..123216398,2	MCF-7	breast:
3	chr12:123205952..123207948-chr12:123213167..123215455,2	K562	blood:
4	chr12:123204711..123206759-chr12:123209537..123212379,2	MCF-7	breast:
5	chr12:123186486..123188573-chr12:123199930..123201817,2	MCF-7	breast:
6	chr12:123201536..123203616-chr12:123208338..123210644,2	MCF-7	breast:
7	chr12:123201536..123203616-chr12:123208338..123210644,2	MCF-7	breast:
8	chr12:123210768..123212595-chr12:123213230..123215441,2	MCF-7	breast:
9	chr12:123210591..123212657-chr12:123213454..123215681,5	MCF-7	breast:
10	chr12:123210591..123212657-chr12:123213454..123215681,5	MCF-7	breast:
11	chr12:123212708..123217136-chr12:123232023..123237517,8	MCF-7	breast:
12	chr12:123210768..123212595-chr12:123213230..123215441,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DENR-2	chr12:123198838-123199340	ENSG00000256249
2	lnc-DENR-2	chr12:123200008-123200255	ENSG00000256249
3	lnc-HCAR3-1	chr12:123210623-123211051	ENSG00000270134.1
4	lnc-DENR-2	chr12:123199801-123200187	NONHSAT031529

No data

Variant related genes	Relation type
HCAR3	TF binding region
ENSG00000256249	TF binding region
ENSG00000270134	TF binding region
HCAR2	TF binding region
HCAR3	CpG island
ENSG00000256249	CpG island
ENSG00000270134	CpG island
HCAR2	CpG island
ENSG00000182782	chromatin interactions
ENSG00000256044	chromatin interactions
ENSG00000139726	chromatin interactions
ENSG00000270134	chromatin interactions
ENSG00000196917	chromatin interactions
LRRC41	miRNA target sites
GALNT11	miRNA target sites

Extended variants
information (count: 874 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:874 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181769950	chr12:123192311-123192312	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs2936779	chr12:123192335-123192336	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs573142124	chr12:123192340-123192341	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs540259974	chr12:123192393-123192394	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs373079298	chr12:123192412-123192413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140732731	chr12:123192422-123192423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547202189	chr12:123192450-123192451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs526276	chr12:123192454-123192455	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs544742600	chr12:123192455-123192456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs632658	chr12:123192467-123192468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2649984	chr12:123192508-123192509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186501126	chr12:123192510-123192511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs111799370	chr12:123192521-123192522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs632260	chr12:123192527-123192528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528427734	chr12:123192566-123192567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs11059476	chr12:123192599-123192600	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs571248401	chr12:123192604-123192605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538316668	chr12:123192630-123192631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188147617	chr12:123192731-123192732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs117195351	chr12:123192738-123192739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536448301	chr12:123192758-123192759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs71308024	chr12:123192808-123192809	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs548572887	chr12:123192846-123192847	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs2454705	chr12:123192848-123192849	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
25	rs540953699	chr12:123192909-123192910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558654202	chr12:123192917-123192918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112497323	chr12:123192941-123192942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373391642	chr12:123192992-123192993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11059480	chr12:123193014-123193015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577326905	chr12:123193042-123193043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544679557	chr12:123193068-123193069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371164523	chr12:123193071-123193072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562975866	chr12:123193109-123193110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530265952	chr12:123193110-123193111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542448105	chr12:123193119-123193120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561172545	chr12:123193144-123193145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375009420	chr12:123193153-123193154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs180796342	chr12:123193193-123193194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528354532	chr12:123193217-123193218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370863407	chr12:123193223-123193224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113986231	chr12:123193251-123193252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370458927	chr12:123193286-123193287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564689942	chr12:123193298-123193299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368120449	chr12:123193309-123193310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550213270	chr12:123193327-123193328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374433955	chr12:123193331-123193332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560858925	chr12:123193370-123193371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs71085842	chr12:123193398-123193399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs11503060	chr12:123193405-123193406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371206048	chr12:123193433-123193434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
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
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
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	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
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD

Chromatin state (count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123174000-123199800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr12:123187800-123198600	Weak transcription	Adipose Nuclei	Adipose
3	chr12:123188000-123193600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr12:123190400-123195000	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr12:123192000-123192600	Enhancers	HepG2	liver
6	chr12:123192600-123199800	Weak transcription	HepG2	liver
7	chr12:123193600-123193800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr12:123193800-123194200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr12:123194200-123194800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr12:123194400-123195600	Enhancers	Placenta	Placenta
11	chr12:123194400-123196000	Enhancers	NHEK	skin
12	chr12:123194600-123195200	Enhancers	Fetal Intestine Large	intestine
13	chr12:123194800-123195800	Enhancers	HMEC	breast
14	chr12:123195000-123195400	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr12:123195000-123195400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:123195000-123195600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:123195000-123195600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr12:123195400-123196000	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr12:123195400-123196600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
20	chr12:123195400-123198600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr12:123195400-123202200	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr12:123195600-123196000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr12:123195600-123198800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr12:123195600-123200000	Weak transcription	Placenta	Placenta
25	chr12:123195800-123198800	Weak transcription	HMEC	breast
26	chr12:123196000-123196200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr12:123196000-123196200	Enhancers	GM12878-XiMat	blood
28	chr12:123196000-123196400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr12:123196000-123197200	Weak transcription	NHEK	skin
30	chr12:123196200-123198600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr12:123196200-123200800	Weak transcription	GM12878-XiMat	blood
32	chr12:123196400-123198800	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr12:123196600-123196800	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr12:123196800-123197400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
35	chr12:123197200-123197800	Enhancers	NHEK	skin
36	chr12:123197400-123197600	Active TSS	Primary neutrophils fromperipheralblood	blood
37	chr12:123197600-123197800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
38	chr12:123197800-123198800	Active TSS	Primary neutrophils fromperipheralblood	blood
39	chr12:123197800-123198800	Weak transcription	NHEK	skin
40	chr12:123198600-123198800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr12:123198600-123198800	Enhancers	Adipose Nuclei	Adipose
42	chr12:123198600-123199200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr12:123198800-123199000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:123198800-123199000	Enhancers	Spleen	Spleen
45	chr12:123198800-123199200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr12:123198800-123199200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
47	chr12:123198800-123199200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr12:123198800-123199200	Flanking Active TSS	Adipose Nuclei	Adipose
49	chr12:123198800-123199400	Enhancers	HMEC	breast
50	chr12:123198800-123199400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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