Variant report

Variant	nsv602128
Chromosome Location	chr6:32433759-32519272
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:601)
CpG islands
(count:2381)
Chromatin interactive
region (count:16)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:601 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:32441356-32441603	K562	blood:	n/a	n/a
2	ATF1	chr6:32443384-32443601	K562	blood:	n/a	n/a
3	BACH1	chr6:32440601-32440675	K562	blood:	n/a	n/a
4	BATF	chr6:32498191-32498485	GM12878	blood:	n/a	n/a
5	BATF	chr6:32441263-32441838	GM12878	blood:	n/a	n/a
6	BATF	chr6:32497788-32498190	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:32497757-32498420	GM12878	blood:	n/a	n/a
8	BCLAF1	chr6:32440393-32441925	GM12878	blood:	n/a	n/a
9	BCLAF1	chr6:32440374-32441401	GM12878	blood:	n/a	n/a
10	BCLAF1	chr6:32497559-32498097	GM12878	blood:	n/a	n/a
11	BCLAF1	chr6:32497233-32498192	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:32498065-32498253	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:32493926-32494025	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:32441347-32441706	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:32517788-32517836	K562	blood:	n/a	n/a
16	CEBPB	chr6:32498060-32498200	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr6:32443372-32443570	K562	blood:	n/a	n/a
18	CEBPB	chr6:32441285-32441529	K562	blood:	n/a	chr6:32441418-32441431
19	CEBPB	chr6:32441175-32441630	MCF-7	breast:	n/a	chr6:32441418-32441431
20	CEBPB	chr6:32441238-32441567	K562	blood:	n/a	chr6:32441418-32441431
21	CEBPB	chr6:32441263-32441593	K562	blood:	n/a	chr6:32441418-32441431
22	CEBPB	chr6:32441197-32441569	MCF-7	breast:	n/a	chr6:32441418-32441431
23	CEBPB	chr6:32439228-32439505	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:32498063-32498112	K562	blood:	n/a	n/a
25	CEBPB	chr6:32504062-32504262	A549	lung:	n/a	n/a
26	CEBPB	chr6:32441368-32441573	H1-hESC	embryonic stem cell:	n/a	chr6:32441418-32441431
27	CHD1	chr6:32441573-32441770	GM12878	blood:	n/a	n/a
28	CHD1	chr6:32497360-32498091	GM12878	blood:	n/a	n/a
29	CHD1	chr6:32439451-32439466	GM12878	blood:	n/a	n/a
30	CHD1	chr6:32440915-32441307	GM12878	blood:	n/a	n/a
31	CHD2	chr6:32497862-32498076	GM12878	blood:	n/a	n/a
32	CHD2	chr6:32440569-32440726	GM12878	blood:	n/a	n/a
33	CHD2	chr6:32441156-32441715	GM12878	blood:	n/a	n/a
34	CREB1	chr6:32441162-32441776	GM12878	blood:	n/a	n/a
35	CREB1	chr6:32497839-32498347	GM12878	blood:	n/a	n/a
36	CREB1	chr6:32440638-32441803	GM12878	blood:	n/a	n/a
37	CREB1	chr6:32441253-32441662	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr6:32445760-32445827	GM19238	blood:	n/a	n/a
39	CTCF	chr6:32489686-32489782	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:32445600-32445750	GM12872	blood:	n/a	n/a
41	CTCF	chr6:32489687-32489692	MCF-7	breast:	n/a	n/a
42	CTCF	chr6:32443734-32443938	HepG2	liver:	n/a	n/a
43	CTCF	chr6:32445660-32445810	MCF-7	breast:	n/a	n/a
44	CTCF	chr6:32445682-32445926	LNCaP	prostate:	n/a	n/a
45	CTCF	chr6:32445720-32445870	K562	blood:	n/a	n/a
46	CTCF	chr6:32445651-32445850	LNCaP	prostate:	n/a	n/a
47	CTCF	chr6:32445735-32445852	GM19239	blood:	n/a	n/a
48	CTCF	chr6:32445720-32445870	GM12872	blood:	n/a	n/a
49	CTCF	chr6:32445713-32445884	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:32497924-32497957	GM19240	blood:	n/a	n/a

(count:2381 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:32489203-32489253	K562	blood:	n/a
2	chr6:32489801-32489851	HCF	heart:	n/a
3	chr6:32489203-32489253	K562	blood:	n/a
4	chr6:32489801-32489851	HCF	heart:	n/a
5	chr6:32493873-32493923	H1-hESC	embryonic stem cell:	embryo
6	chr6:32499368-32499418	GM19239	blood:	n/a
7	chr6:32452388-32452438	AG09319	gingival:	n/a
8	chr6:32493917-32493967	AG04449	skin:	fetal
9	chr6:32490350-32490400	GM19239	blood:	n/a
10	chr6:32489555-32489605	LNCaP	prostate:	n/a
11	chr6:32499368-32499418	HCM	heart:	n/a
12	chr6:32498677-32498727	AG09319	gingival:	n/a
13	chr6:32451079-32451129	SAEC	small airway:	n/a
14	chr6:32499860-32499910	HCF	heart:	n/a
15	chr6:32491826-32491876	NHBE	bronchial:	n/a
16	chr6:32515773-32515823	HRPEpiC	eye:	n/a
17	chr6:32493917-32493967	ovcar-3	ovarian:	n/a
18	chr6:32515150-32515200	HPAEpiC	pulmonary alveolar:	n/a
19	chr6:32495746-32495796	RPTEC	kidney:	n/a
20	chr6:32489750-32489800	SK-N-SH_RA	brain:	n/a
21	chr6:32495746-32495796	GM19239	blood:	n/a
22	chr6:32486399-32486449	GM12892	blood:	n/a
23	chr6:32516004-32516054	NH-A	brain:	n/a
24	chr6:32489984-32490034	HCT-116	colon:	n/a
25	chr6:32515150-32515200	PFSK-1	brain:	n/a
26	chr6:32496326-32496376	NHBE	bronchial:	n/a
27	chr6:32489553-32489603	HL-60	blood:	n/a
28	chr6:32490444-32490494	AoSMC	blood vessel:	n/a
29	chr6:32486399-32486449	BJ	skin:	n/a
30	chr6:32489963-32490013	SAEC	small airway:	n/a
31	chr6:32487314-32487364	ovcar-3	ovarian:	n/a
32	chr6:32490421-32490471	NHBE	bronchial:	n/a
33	chr6:32487314-32487364	AG04449	skin:	fetal
34	chr6:32515069-32515119	NB4	blood:	n/a
35	chr6:32498493-32498543	K562	blood:	n/a
36	chr6:32451079-32451129	HEK293	kidney:	embryo
37	chr6:32489750-32489800	PANC-1	pancreas:	n/a
38	chr6:32487314-32487364	GM12892	blood:	n/a
39	chr6:32489984-32490034	HL-60	blood:	n/a
40	chr6:32489963-32490013	AoSMC	blood vessel:	n/a
41	chr6:32490444-32490494	MCF10A-Er-Src	breast:	n/a
42	chr6:32499860-32499910	NH-A	brain:	n/a
43	chr6:32498493-32498543	SK-N-MC	brain:	n/a
44	chr6:32452388-32452438	HCPEpiC	choroid plexus:	n/a
45	chr6:32498493-32498543	ovcar-3	ovarian:	n/a
46	chr6:32490043-32490093	SAEC	small airway:	n/a
47	chr6:32490012-32490062	Jurkat	blood:	n/a
48	chr6:32486399-32486449	K562	blood:	n/a
49	chr6:32466447-32466497	AG04449	skin:	fetal
50	chr6:32486399-32486449	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:32400824..32401535-chr6:32443504..32444248,2	MCF-7	breast:
2	chr6:32496441..32498666-chr6:32501268..32503290,2	MCF-7	breast:
3	chr6:32432882..32434661-chr6:32437882..32440556,2	K562	blood:
4	chr6:32399459..32400332-chr6:32443390..32444188,2	MCF-7	breast:
5	chr6:32428191..32430542-chr6:32458841..32460810,2	MCF-7	breast:
6	chr6:32478863..32481240-chr6:32540968..32542884,2	K562	blood:
7	chr6:32492411..32495450-chr6:32552484..32555959,3	MCF-7	breast:
8	chr6:32383034..32383683-chr6:32443303..32444621,3	MCF-7	breast:
9	chr6:32489338..32491320-chr6:32492335..32495194,2	MCF-7	breast:
10	chr6:32086283..32087229-chr6:32443372..32443883,2	K562	blood:
11	chr6:32488425..32491082-chr6:32525421..32528152,2	MCF-7	breast:
12	chr6:32432882..32434661-chr6:32437882..32440556,2	K562	blood:
13	chr6:32446571..32447329-chr6:32534338..32534901,2	MCF-7	breast:
14	chr6:32497873..32498399-chr6:32557101..32557832,2	HCT-116	colon:
15	chr6:32483984..32486232-chr6:32528948..32530708,2	MCF-7	breast:
16	chr6:32489338..32491320-chr6:32492335..32495194,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HLA-DRB5-1	chr6:32441202-32441277	NONHSAT108907
2	lnc-HLA-DRA-4	chr6:32474307-32474692	NONHSAT108908
3	lnc-HLA-DRA-5	chr6:32475256-32475512	NONHSAT108909
4	lnc-HLA-DQA1-7	chr6:32487174-32487196	NONHSAT108910

No data

Variant related genes	Relation type
RNU1-61P	TF binding region
HLA-DRB9	TF binding region
HLA-DRB5	TF binding region
RNU1-61P	CpG island
HLA-DRB9	CpG island
HLA-DRB5	CpG island
ENSG00000196126	chromatin interactions
ENSG00000198502	chromatin interactions
ENSG00000229391	chromatin interactions

Extended variants
information (count: 5737 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:5737 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9405038	chr6:32437614-32437615	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551739497	chr6:32437618-32437619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563766769	chr6:32437622-32437623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528146333	chr6:32437637-32437638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs9269030	chr6:32437684-32437685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147925392	chr6:32437701-32437702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530128299	chr6:32437706-32437707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182341441	chr6:32437744-32437745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs9269031	chr6:32437747-32437748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs9269032	chr6:32437754-32437755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186988980	chr6:32437767-32437768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191785247	chr6:32437813-32437814	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
13	rs202182258	chr6:32437835-32437836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139783142	chr6:32437844-32437845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147113013	chr6:32437845-32437846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566885563	chr6:32437848-32437849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142996546	chr6:32437859-32437860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201830763	chr6:32437896-32437897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9269035	chr6:32437912-32437913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs9269036	chr6:32437917-32437918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9269037	chr6:32437958-32437959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs9269038	chr6:32437996-32437997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545713224	chr6:32437997-32437998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190040608	chr6:32438000-32438001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528079816	chr6:32438017-32438018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201174005	chr6:32438031-32438032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201973603	chr6:32438035-32438036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539888364	chr6:32438043-32438044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375927363	chr6:32438048-32438049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs9269039	chr6:32438049-32438050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201335103	chr6:32438063-32438064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs9269040	chr6:32438080-32438081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550875549	chr6:32438121-32438122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375534168	chr6:32438148-32438149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs9368725	chr6:32438159-32438160	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs533635643	chr6:32438168-32438169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs28732237	chr6:32438194-32438195	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs373519508	chr6:32438210-32438211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs9269041	chr6:32438243-32438244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9380306	chr6:32438298-32438299	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs538268830	chr6:32438341-32438342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559266601	chr6:32438354-32438355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9269042	chr6:32438387-32438388	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs138653953	chr6:32438426-32438427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538364445	chr6:32438466-32438467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556849277	chr6:32438506-32438507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141904748	chr6:32438511-32438512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12524496	chr6:32438513-32438514	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs9368726	chr6:32438542-32438543	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs12525692	chr6:32438546-32438547	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:131)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Ovarian cancer	21781307	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	22522925	CNVD
Rheumatoid arthritis	22536334	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:32437600-32441000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:32439200-32439400	Active TSS	Primary B cells from peripheral blood	blood
3	chr6:32439200-32439400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:32439200-32439400	Active TSS	GM12878-XiMat	blood
5	chr6:32439200-32439400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr6:32439200-32439600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
7	chr6:32439200-32440800	Active TSS	Primary B cells from cord blood	blood
8	chr6:32439400-32439600	Bivalent/Poised TSS	Primary Natural Killer cells fromperipheralblood	blood
9	chr6:32439400-32439600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr6:32439400-32439600	Active TSS	Monocytes-CD14+_RO01746	blood
11	chr6:32439400-32439800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:32439400-32440000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:32439400-32440200	Active TSS	Primary monocytes fromperipheralblood	blood
14	chr6:32439400-32440200	Flanking Active TSS	Primary B cells from peripheral blood	blood
15	chr6:32439400-32440800	ZNF genes & repeats	GM12878-XiMat	blood
16	chr6:32439600-32440200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr6:32439600-32441000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
18	chr6:32439600-32442200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr6:32439800-32440600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr6:32440200-32440400	Active TSS	Primary B cells from peripheral blood	blood
21	chr6:32440200-32440800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr6:32440200-32441000	Active TSS	Primary hematopoietic stem cells short term culture	blood
23	chr6:32440200-32441200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
24	chr6:32440200-32441800	Enhancers	Primary hematopoietic stem cells	blood
25	chr6:32440400-32442200	Flanking Active TSS	Primary B cells from peripheral blood	blood
26	chr6:32440600-32441000	Active TSS	Adipose Nuclei	Adipose
27	chr6:32440600-32441800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr6:32440600-32441800	Active TSS	Brain Anterior Caudate	brain
29	chr6:32440800-32441200	Flanking Active TSS	Primary B cells from cord blood	blood
30	chr6:32440800-32441400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr6:32440800-32442200	Flanking Active TSS	GM12878-XiMat	blood
32	chr6:32441000-32441200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr6:32441000-32441400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr6:32441000-32441400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr6:32441000-32441400	Flanking Active TSS	Adipose Nuclei	Adipose
36	chr6:32441000-32441400	Enhancers	Fetal Thymus	thymus
37	chr6:32441000-32441800	Enhancers	Duodenum Mucosa	Duodenum
38	chr6:32441000-32441800	Active TSS	Rectal Mucosa Donor 29	rectum
39	chr6:32441000-32441800	Enhancers	Spleen	Spleen
40	chr6:32441000-32442200	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr6:32441000-32442400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr6:32441200-32441400	Enhancers	Colonic Mucosa	Colon
43	chr6:32441200-32442200	Enhancers	Primary B cells from cord blood	blood
44	chr6:32441200-32442800	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr6:32441400-32441600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr6:32441600-32441800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr6:32441800-32442200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr6:32441800-32442400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr6:32441800-32444600	Weak transcription	Duodenum Mucosa	Duodenum
50	chr6:32441800-32445400	Weak transcription	Brain Anterior Caudate	brain

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