Variant report

Variant	nsv970030
Chromosome Location	chr6:27880682-27909942
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:27908618-27908866	K562	blood:	n/a	n/a
2	ATF1	chr6:27908604-27908854	K562	blood:	n/a	n/a
3	ATF3	chr6:27908522-27908861	K562	blood:	n/a	n/a
4	BACH1	chr6:27905930-27905955	K562	blood:	n/a	n/a
5	CBX3	chr6:27908533-27908904	K562	blood:	n/a	n/a
6	CCNT2	chr6:27908660-27908818	K562	blood:	n/a	n/a
7	CEBPB	chr6:27902904-27903120	HepG2	liver:	n/a	chr6:27902999-27903010
8	CEBPB	chr6:27899099-27899316	HepG2	liver:	n/a	chr6:27899205-27899216
9	CEBPB	chr6:27899131-27899246	K562	blood:	n/a	chr6:27899205-27899216
10	CEBPB	chr6:27908564-27908958	K562	blood:	n/a	n/a
11	CEBPD	chr6:27908488-27908996	K562	blood:	n/a	n/a
12	CREB1	chr6:27898967-27899442	K562	blood:	n/a	n/a
13	CTCF	chr6:27898009-27898053	Fibrobl	skin:	n/a	n/a
14	CTCF	chr6:27900660-27900711	Lung_OC	lung:	n/a	n/a
15	CTCF	chr6:27896500-27896650	HepG2	liver:	n/a	n/a
16	CTCF	chr6:27891701-27891752	GM20000	blood:	n/a	n/a
17	CUX1	chr6:27887384-27887567	K562	blood:	n/a	n/a
18	CUX1	chr6:27890200-27890234	K562	blood:	n/a	n/a
19	EP300	chr6:27908612-27908866	K562	blood:	n/a	chr6:27908689-27908698 chr6:27908690-27908699
20	EP300	chr6:27886541-27886711	K562	blood:	n/a	n/a
21	EP300	chr6:27908476-27908801	K562	blood:	n/a	chr6:27908689-27908698 chr6:27908690-27908699
22	FOS	chr6:27908597-27908807	MCF10A-Er-Src	breast:	n/a	chr6:27908691-27908702 chr6:27908690-27908698 chr6:27908689-27908698 chr6:27908690-27908697 chr6:27908688-27908700
23	FOS	chr6:27908660-27908867	MCF10A-Er-Src	breast:	n/a	chr6:27908691-27908702 chr6:27908690-27908698 chr6:27908689-27908698 chr6:27908690-27908697 chr6:27908688-27908700
24	FOS	chr6:27908631-27908831	MCF10A-Er-Src	breast:	n/a	chr6:27908691-27908702 chr6:27908690-27908698 chr6:27908689-27908698 chr6:27908690-27908697 chr6:27908688-27908700
25	FOS	chr6:27908612-27908753	MCF10A-Er-Src	breast:	n/a	chr6:27908691-27908702 chr6:27908690-27908698 chr6:27908689-27908698 chr6:27908690-27908697 chr6:27908688-27908700
26	FOSL1	chr6:27908562-27908857	K562	blood:	n/a	chr6:27908691-27908702 chr6:27908690-27908698 chr6:27908689-27908698 chr6:27908690-27908697 chr6:27908688-27908700
27	GATA2	chr6:27900958-27901132	SH-SY5Y	brain:	n/a	n/a
28	GATA2	chr6:27908462-27908989	K562	blood:	n/a	chr6:27908691-27908700
29	HEY1	chr6:27896783-27897037	K562	blood:	n/a	n/a
30	JUN	chr6:27899023-27899304	HepG2	liver:	n/a	chr6:27899153-27899162 chr6:27899149-27899162
31	JUN	chr6:27908538-27908882	K562	blood:	n/a	chr6:27908691-27908702 chr6:27908690-27908698 chr6:27908689-27908698 chr6:27908690-27908697 chr6:27908688-27908700
32	JUN	chr6:27908584-27908925	K562	blood:	n/a	chr6:27908691-27908702 chr6:27908690-27908698 chr6:27908689-27908698 chr6:27908690-27908697 chr6:27908688-27908700
33	JUN	chr6:27908591-27908890	K562	blood:	n/a	chr6:27908691-27908702 chr6:27908690-27908698 chr6:27908689-27908698 chr6:27908690-27908697 chr6:27908688-27908700
34	JUND	chr6:27899011-27899295	HepG2	liver:	n/a	chr6:27899153-27899162
35	JUND	chr6:27908639-27908833	HepG2	liver:	n/a	chr6:27908691-27908702 chr6:27908690-27908698 chr6:27908689-27908698 chr6:27908690-27908697 chr6:27908688-27908700 chr6:27908688-27908699
36	JUND	chr6:27908527-27908919	K562	blood:	n/a	chr6:27908691-27908702 chr6:27908690-27908698 chr6:27908689-27908698 chr6:27908690-27908697 chr6:27908688-27908700 chr6:27908688-27908699
37	MAFF	chr6:27885377-27885630	HepG2	liver:	n/a	n/a
38	MAFF	chr6:27890867-27891008	K562	blood:	n/a	chr6:27890938-27890956
39	MAFF	chr6:27890798-27891085	HepG2	liver:	n/a	chr6:27890938-27890956
40	MAFK	chr6:27883244-27883259	HepG2	liver:	n/a	n/a
41	MAFK	chr6:27890849-27891087	HepG2	liver:	n/a	n/a
42	MAFK	chr6:27885338-27885673	HepG2	liver:	n/a	n/a
43	MAFK	chr6:27883205-27883299	HepG2	liver:	n/a	chr6:27883264-27883279 chr6:27883261-27883277 chr6:27883259-27883279
44	MAFK	chr6:27885435-27885630	IMR90	lung:	n/a	n/a
45	MAFK	chr6:27885362-27885629	HepG2	liver:	n/a	n/a
46	MAFK	chr6:27891463-27891649	HepG2	liver:	n/a	n/a
47	MAFK	chr6:27890858-27891033	K562	blood:	n/a	n/a
48	MAZ	chr6:27888049-27888206	HepG2	liver:	n/a	n/a
49	NR2F2	chr6:27908480-27908907	K562	blood:	n/a	n/a
50	NR2F2	chr6:27908541-27908913	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:27880822-27880872	NHBE	bronchial:	n/a
2	chr6:27880822-27880872	ProgFib	skin:	n/a
3	chr6:27880954-27881004	SAEC	small airway:	n/a
4	chr6:27880822-27880872	NH-A	brain:	n/a
5	chr6:27880822-27880872	HIPEpiC	eye:	n/a
6	chr6:27880822-27880872	LNCaP	prostate:	n/a
7	chr6:27880954-27881004	BE2_C	brain:	n/a
8	chr6:27880954-27881004	ovcar-3	ovarian:	n/a
9	chr6:27880954-27881004	HCF	heart:	n/a
10	chr6:27880954-27881004	HCPEpiC	choroid plexus:	n/a
11	chr6:27880822-27880872	MCF10A-Er-Src	breast:	n/a
12	chr6:27880954-27881004	HL-60	blood:	n/a
13	chr6:27881242-27881292	RPTEC	kidney:	n/a
14	chr6:27880954-27881004	ProgFib	skin:	n/a
15	chr6:27881242-27881292	HEK293	kidney:	embryo
16	chr6:27880822-27880872	AG10803	skin:	n/a
17	chr6:27880954-27881004	RPTEC	kidney:	n/a
18	chr6:27880822-27880872	Jurkat	blood:	n/a
19	chr6:27880822-27880872	HCT-116	colon:	n/a
20	chr6:27880822-27880872	T-47D	breast:	n/a
21	chr6:27880822-27880872	PFSK-1	brain:	n/a
22	chr6:27881242-27881292	HUVEC	blood vessel:	n/a
23	chr6:27881242-27881292	PFSK-1	brain:	n/a
24	chr6:27880954-27881004	NHDF-neo	bronchial:	n/a
25	chr6:27880822-27880872	AG09309	skin:	n/a
26	chr6:27880954-27881004	SK-N-MC	brain:	n/a
27	chr6:27880822-27880872	U87	brain:	n/a
28	chr6:27880954-27881004	PANC-1	pancreas:	n/a
29	chr6:27881242-27881292	HCF	heart:	n/a
30	chr6:27881242-27881292	IMR90	lung:	fetal
31	chr6:27881242-27881292	H1-hESC	embryonic stem cell:	embryo
32	chr6:27880822-27880872	A549	lung:	n/a
33	chr6:27881242-27881292	NB4	blood:	n/a
34	chr6:27881242-27881292	AG09319	gingival:	n/a
35	chr6:27880822-27880872	GM12878	blood:	n/a
36	chr6:27881242-27881292	PrEC	prostate:	n/a
37	chr6:27880954-27881004	PrEC	prostate:	n/a
38	chr6:27881242-27881292	HMEC	breast:	n/a
39	chr6:27880954-27881004	A549	lung:	n/a
40	chr6:27880822-27880872	Hepatocyte	liver:	n/a
41	chr6:27880954-27881004	HCT-116	colon:	n/a
42	chr6:27881242-27881292	CMK	blood:	n/a
43	chr6:27880954-27881004	HIPEpiC	eye:	n/a
44	chr6:27880954-27881004	IMR90	lung:	fetal
45	chr6:27880822-27880872	AG09319	gingival:	n/a
46	chr6:27880954-27881004	NB4	blood:	n/a
47	chr6:27881242-27881292	HepG2	liver:	n/a
48	chr6:27881242-27881292	ovcar-3	ovarian:	n/a
49	chr6:27880822-27880872	AG04450	lung:	fetal
50	chr6:27880822-27880872	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:27906019..27908649-chr6:27909756..27911913,2	K562	blood:
2	chr6:27900872..27904331-chr6:27905533..27908216,3	K562	blood:
3	chr6:27869224..27870861-chr6:27906811..27908499,2	K562	blood:
4	chr6:27900872..27904331-chr6:27905533..27908216,3	K562	blood:
5	chr6:27890672..27893194-chr6:27950169..27951768,2	K562	blood:
6	chr6:27884862..27886934-chr6:27890220..27891868,2	MCF-7	breast:
7	chr6:27888989..27890885-chr6:27892239..27894866,2	MCF-7	breast:
8	chr6:27857667..27861764-chr6:27891119..27894873,6	K562	blood:
9	chr6:27882241..27884858-chr6:27901500..27903298,2	K562	blood:
10	chr6:27882241..27884858-chr6:27901500..27903298,2	K562	blood:
11	chr6:27884862..27886934-chr6:27890220..27891868,2	MCF-7	breast:
12	chr6:27778583..27780437-chr6:27901055..27904160,3	K562	blood:
13	chr6:27894600..27896856-chr6:27897179..27899651,3	K562	blood:
14	chr6:27906019..27908649-chr6:27909756..27911913,2	K562	blood:
15	chr6:27890558..27893641-chr6:27899423..27901654,3	K562	blood:
16	chr6:27774964..27777447-chr6:27902670..27905065,2	K562	blood:
17	chr6:27901905..27904183-chr6:28041057..28044024,2	K562	blood:
18	chr6:27880639..27883461-chr7:11306851..11309270,2	MCF-7	breast:
19	chr6:27890558..27893641-chr6:27899423..27901654,3	K562	blood:
20	chr6:27905285..27912363-chr6:27912383..27920173,13	K562	blood:
21	chr6:27877630..27879504-chr6:27883396..27885333,2	MCF-7	breast:
22	chr6:27888989..27890885-chr6:27892239..27894866,2	MCF-7	breast:
23	chr6:27859035..27860980-chr6:27897305..27900067,2	K562	blood:
24	chr6:27894600..27896856-chr6:27897179..27899651,3	K562	blood:
25	chr6:27868676..27871582-chr6:27889227..27891930,6	K562	blood:

Variant related genes	Relation type
OR2B2	TF binding region
OR2W6P	TF binding region
OR2B2	CpG island
OR2W6P	CpG island
ENSG00000197153	chromatin interactions
ENSG00000233224	chromatin interactions
ENSG00000220721	chromatin interactions
ENSG00000196331	chromatin interactions
ENSG00000196747	chromatin interactions
ENSG00000185130	chromatin interactions

Extended variants
information (count: 915 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555858185	chr6:27880720-27880721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs546469219	chr6:27880757-27880758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190576417	chr6:27880821-27880822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149318186	chr6:27880842-27880843	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs373568163	chr6:27880896-27880897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs56219068	chr6:27880904-27880905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541688680	chr6:27880968-27880969	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs144573038	chr6:27881003-27881004	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs533622318	chr6:27881016-27881017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139296255	chr6:27881020-27881021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563100578	chr6:27881038-27881039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183054075	chr6:27881085-27881086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12181629	chr6:27881147-27881148	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs565484049	chr6:27881198-27881199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528259710	chr6:27881243-27881244	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs76682782	chr6:27881270-27881271	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs556802844	chr6:27881313-27881314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145970942	chr6:27881359-27881360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536914028	chr6:27881360-27881361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139851179	chr6:27881382-27881383	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs9885649	chr6:27881406-27881407	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs115639664	chr6:27881420-27881421	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs552330126	chr6:27881461-27881462	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs555572649	chr6:27881515-27881516	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs142070500	chr6:27881532-27881533	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs370187259	chr6:27881551-27881552	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs368286251	chr6:27881554-27881555	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs558353649	chr6:27881562-27881563	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs578226273	chr6:27881589-27881590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543740147	chr6:27881620-27881621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs151139454	chr6:27881623-27881624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186375860	chr6:27881654-27881655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538398369	chr6:27881671-27881672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140019722	chr6:27881686-27881687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs75249060	chr6:27881721-27881722	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs149851646	chr6:27881775-27881776	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs551078182	chr6:27881794-27881795	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs147945313	chr6:27881809-27881810	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs200945	chr6:27881904-27881905	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs550598360	chr6:27881915-27881916	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs567594997	chr6:27882097-27882098	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115150975	chr6:27882115-27882116	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549352620	chr6:27882220-27882221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535084416	chr6:27882224-27882225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558315413	chr6:27882226-27882227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs578199381	chr6:27882356-27882357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547160262	chr6:27882367-27882368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs202195532	chr6:27882388-27882389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190986675	chr6:27882408-27882409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182690996	chr6:27882418-27882419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	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
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	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
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27871600-27883200	Weak transcription	Hela-S3	cervix
2	chr6:27880000-27881800	Weak transcription	K562	blood
3	chr6:27880200-27881400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:27881400-27881600	Enhancers	Primary hematopoietic stem cells	blood
5	chr6:27881400-27881600	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr6:27881400-27882400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr6:27881400-27882400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr6:27881800-27882200	Strong transcription	K562	blood
9	chr6:27882000-27882200	Enhancers	Primary hematopoietic stem cells	blood
10	chr6:27882200-27882400	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr6:27882200-27886800	Weak transcription	K562	blood
12	chr6:27886600-27886800	Bivalent/Poised TSS	Primary Natural Killer cells fromperipheralblood	blood
13	chr6:27886800-27892600	Strong transcription	K562	blood
14	chr6:27892000-27892400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr6:27892000-27892400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:27892000-27892400	Enhancers	NHEK	skin
17	chr6:27892600-27893800	Weak transcription	K562	blood
18	chr6:27893800-27895800	Strong transcription	K562	blood
19	chr6:27895800-27896400	Weak transcription	K562	blood
20	chr6:27896400-27896800	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr6:27896400-27898800	Strong transcription	K562	blood
22	chr6:27898800-27900600	Weak transcription	K562	blood
23	chr6:27900600-27901200	Enhancers	K562	blood
24	chr6:27901200-27902400	Weak transcription	K562	blood
25	chr6:27902400-27908600	Strong transcription	K562	blood
26	chr6:27908600-27909600	Genic enhancers	K562	blood
27	chr6:27909600-27913600	Weak transcription	K562	blood

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