Variant report

Variant	nsv994947
Chromosome Location	chr6:163083-184838
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	chr6:168940-169157	HepG2	liver:	n/a	n/a
2	ATF2	chr6:181047-181898	GM12878	blood:	n/a	n/a
3	ATF2	chr6:181000-181701	GM12878	blood:	n/a	n/a
4	BATF	chr6:183781-184092	GM12878	blood:	n/a	n/a
5	BATF	chr6:181320-181669	GM12878	blood:	n/a	n/a
6	BATF	chr6:181382-181622	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:181394-181586	GM12878	blood:	n/a	chr6:181481-181490
8	BCL3	chr6:181242-181640	GM12878	blood:	n/a	chr6:181481-181490
9	BCLAF1	chr6:181165-181751	GM12878	blood:	n/a	chr6:181481-181490
10	BHLHE40	chr6:181240-181647	GM12878	blood:	n/a	n/a
11	BRCA1	chr6:181184-181190	GM12878	blood:	n/a	n/a
12	CEBPB	chr6:175194-175390	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr6:168881-169126	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:167122-167477	K562	blood:	n/a	chr6:167228-167239
15	CEBPB	chr6:180266-180564	K562	blood:	n/a	n/a
16	CEBPB	chr6:168881-169187	K562	blood:	n/a	n/a
17	CEBPB	chr6:168835-169203	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:167108-167420	HepG2	liver:	n/a	chr6:167228-167239
19	CEBPB	chr6:167215-167379	H1-hESC	embryonic stem cell:	n/a	chr6:167228-167239
20	CEBPB	chr6:174130-174338	HepG2	liver:	n/a	chr6:174244-174255
21	CEBPB	chr6:168922-169138	A549	lung:	n/a	n/a
22	CEBPB	chr6:167167-167294	K562	blood:	n/a	chr6:167228-167239
23	CEBPB	chr6:167113-167409	Hela-S3	cervix:	n/a	chr6:167228-167239
24	CEBPB	chr6:167170-167315	A549	lung:	n/a	chr6:167228-167239
25	CTCF	chr6:168912-169166	SK-N-SH_RA	brain:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
26	CTCF	chr6:168969-169124	SK-N-SH_RA	brain:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
27	CTCF	chr6:168940-169090	Caco-2	colon:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
28	CTCF	chr6:168960-169110	Caco-2	colon:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
29	CTCF	chr6:169000-169150	AG10803	skin:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
30	CTCF	chr6:169000-169150	AG04449	skin:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
31	CTCF	chr6:168720-168870	AoAF	blood vessel:	n/a	chr6:168807-168815
32	CTCF	chr6:165836-165878	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:168980-169130	GM12872	blood:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
34	CTCF	chr6:168833-169270	GM12878	blood:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
35	CTCF	chr6:168700-168850	GM12875	blood:	n/a	chr6:168807-168815
36	CTCF	chr6:168940-169090	HAc	cerebellar:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
37	CTCF	chr6:168900-169050	HEK293	kidney:	n/a	n/a
38	CTCF	chr6:169060-169210	GM12866	blood:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169065-169073
39	CTCF	chr6:169040-169190	HVMF	connective:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
40	CTCF	chr6:168960-169110	SK-N-SH_RA	brain:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
41	CTCF	chr6:169000-169150	HEK293	kidney:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
42	CTCF	chr6:168720-168870	GM12864	blood:	n/a	chr6:168807-168815
43	CTCF	chr6:168920-169070	HMEC	breast:	n/a	n/a
44	CTCF	chr6:168954-169161	Lung_OC	lung:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
45	CTCF	chr6:168928-169177	GM13977	blood:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
46	CTCF	chr6:168825-169271	IMR90	lung:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
47	CTCF	chr6:169000-169150	HA-sp	spinal cord:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
48	CTCF	chr6:169020-169170	NB4	blood:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
49	CTCF	chr6:169020-169170	HMEC	breast:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073
50	CTCF	chr6:168940-169090	HUVEC	blood vessel:	n/a	chr6:169060-169078 chr6:169061-169077 chr6:169055-169076 chr6:169065-169073

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:179456-179506	GM12891	blood:	n/a
2	chr6:179456-179506	GM12891	blood:	n/a
3	chr6:179659-179709	HCF	heart:	n/a
4	chr6:179456-179506	NHBE	bronchial:	n/a
5	chr6:179456-179506	K562	blood:	n/a
6	chr6:179659-179709	NHDF-neo	bronchial:	n/a
7	chr6:179456-179506	HIPEpiC	eye:	n/a
8	chr6:179456-179506	HCT-116	colon:	n/a
9	chr6:179456-179506	HRE	kidney:	n/a
10	chr6:179659-179709	NHBE	bronchial:	n/a
11	chr6:179456-179506	HCPEpiC	choroid plexus:	n/a
12	chr6:179659-179709	PFSK-1	brain:	n/a
13	chr6:179456-179506	HCF	heart:	n/a
14	chr6:179659-179709	HEEpiC	esophagus:	n/a
15	chr6:179456-179506	IMR90	lung:	fetal
16	chr6:179456-179506	GM06990	blood:	n/a
17	chr6:179659-179709	AoSMC	blood vessel:	n/a
18	chr6:179659-179709	PrEC	prostate:	n/a
19	chr6:179659-179709	SKMC	muscle:	n/a
20	chr6:179456-179506	BE2_C	brain:	n/a
21	chr6:179659-179709	AG09309	skin:	n/a
22	chr6:179456-179506	SK-N-SH_RA	brain:	n/a
23	chr6:179659-179709	H1-hESC	embryonic stem cell:	embryo
24	chr6:179456-179506	AG04449	skin:	fetal
25	chr6:179456-179506	HRPEpiC	eye:	n/a
26	chr6:179456-179506	SKMC	muscle:	n/a
27	chr6:179659-179709	ProgFib	skin:	n/a
28	chr6:179456-179506	SAEC	small airway:	n/a
29	chr6:179456-179506	U87	brain:	n/a
30	chr6:179456-179506	Hepatocyte	liver:	n/a
31	chr6:179659-179709	GM19239	blood:	n/a
32	chr6:179659-179709	PANC-1	pancreas:	n/a
33	chr6:179456-179506	Jurkat	blood:	n/a
34	chr6:179456-179506	HMEC	breast:	n/a
35	chr6:179456-179506	HL-60	blood:	n/a
36	chr6:179456-179506	HEK293	kidney:	embryo
37	chr6:179456-179506	GM12878	blood:	n/a
38	chr6:179456-179506	RPTEC	kidney:	n/a
39	chr6:179456-179506	NT2-D1	testis:	n/a
40	chr6:179456-179506	CMK	blood:	n/a
41	chr6:179659-179709	SK-N-MC	brain:	n/a
42	chr6:179659-179709	SK-N-SH	brain:	n/a
43	chr6:179659-179709	ovcar-3	ovarian:	n/a
44	chr6:179659-179709	CMK	blood:	n/a
45	chr6:179659-179709	HRPEpiC	eye:	n/a
46	chr6:179456-179506	H1-hESC	embryonic stem cell:	embryo
47	chr6:179659-179709	A549	lung:	n/a
48	chr6:179659-179709	HCPEpiC	choroid plexus:	n/a
49	chr6:179659-179709	AG04450	lung:	fetal
50	chr6:179456-179506	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:174671..177385-chr6:182024..184445,2	K562	blood:
2	chr6:181320..184707-chr6:184919..187235,3	K562	blood:
3	chr6:182386..184733-chr6:187298..189526,2	K562	blood:
4	chr6:181476..184276-chr6:186622..188907,2	MCF-7	breast:
5	chr6:178419..181938-chr6:182767..184759,3	K562	blood:
6	chr6:178419..181938-chr6:182767..184759,3	K562	blood:
7	chr6:174671..177385-chr6:182024..184445,2	K562	blood:
8	chr6:162155..164910-chr6:167837..169506,2	K562	blood:
9	chr6:181397..184733-chr6:185247..188798,3	K562	blood:
10	chr6:162155..164910-chr6:167837..169506,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL035696.1-2	chr6:184161-184371	NONHSAT105976
2	lnc-EXOC2-6	chr6:184593-184809	ENSG00000263667.1
3	lnc-EXOC2-20	chr6:169545-169753	NONHSAT105971
4	lnc-AL035696.1-6	chr6:170686-171068	NONHSAT105973
5	lnc-EXOC2-20	chr6:170352-170631	NONHSAT105971
6	lnc-EXOC2-6	chr6:182366-182474	ENSG00000263667.1
7	lnc-AL035696.1-6	chr6:171079-171400	NONHSAT105973
8	lnc-AL035696.1-2	chr6:183914-184371	XLOC_005117
9	lnc-EXOC2-6	chr6:181466-181695	ENSG00000263667.1
10	lnc-EXOC2-20	chr6:168171-170561	NONHSAT105972
11	lnc-EXOC2-20	chr6:167607-167826	NONHSAT105971
12	lnc-AL035696.1-6	chr6:169950-170088	NONHSAT105973
13	lnc-EXOC2-20	chr6:171827-172220	NONHSAT105972
14	lnc-AL035696.1-2	chr6:184601-187741	XLOC_005117

Variant related genes	Relation type
ENSG00000218577	TF binding region
ENSG00000218577	CpG island
TSC1	miRNA target sites
TRRAP	miRNA target sites

Extended variants
information (count: 309 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs719065	chr6:165632-165633	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535378867	chr6:165818-165819	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370612622	chr6:165899-165900	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551791705	chr6:165959-165960	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs57803541	chr6:166095-166096	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs75121857	chr6:166136-166137	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116753945	chr6:166189-166190	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111686581	chr6:166454-166455	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371259285	chr6:166483-166484	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11242666	chr6:166638-166639	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145595179	chr6:166646-166647	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs202156730	chr6:166732-166733	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs578021823	chr6:166746-166747	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs199991782	chr6:166750-166751	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373910961	chr6:166754-166755	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375930006	chr6:166904-166905	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368535590	chr6:167114-167115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371618889	chr6:167127-167128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs374989245	chr6:167131-167132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368526980	chr6:167160-167161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs9502835	chr6:167708-167709	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs73719526	chr6:167749-167750	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs532256716	chr6:167785-167786	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs9502836	chr6:168197-168198	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs369784219	chr6:168248-168249	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs113600288	chr6:168264-168265	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs552195094	chr6:168315-168316	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs377187222	chr6:168410-168411	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs142831339	chr6:168424-168425	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs201305470	chr6:168428-168429	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs559071025	chr6:168466-168467	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs60447526	chr6:168478-168479	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs112541457	chr6:168571-168572	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs114344987	chr6:168801-168802	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs370707845	chr6:168843-168844	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs111246084	chr6:168991-168992	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs568921875	chr6:169054-169055	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs115357777	chr6:169141-169142	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs202175158	chr6:169152-169153	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs115431157	chr6:169257-169258	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs370462685	chr6:169494-169495	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs113086792	chr6:169533-169534	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs200221467	chr6:169632-169633	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs538515352	chr6:169759-169760	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs563426150	chr6:169773-169774	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs139197019	chr6:169795-169796	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs529390246	chr6:169812-169813	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs370950257	chr6:169822-169823	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs111916764	chr6:169958-169959	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs375242098	chr6:170038-170039	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Prader-willi syndrome	20588305	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	22495311	CNVD
small cell lung cancer	20016488	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:165600-167000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:165800-167000	Enhancers	Osteobl	bone
3	chr6:165800-167200	Enhancers	Fetal Muscle Trunk	muscle
4	chr6:166800-167000	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:168600-169000	Enhancers	GM12878-XiMat	blood
6	chr6:174800-178200	Weak transcription	Right Atrium	heart
7	chr6:177200-179600	Weak transcription	Primary B cells from peripheral blood	blood
8	chr6:178200-178400	ZNF genes & repeats	Right Atrium	heart
9	chr6:178200-178400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
10	chr6:178200-178600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
11	chr6:178200-179000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr6:178200-180200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:178400-192200	Weak transcription	Right Atrium	heart
14	chr6:179600-191800	Enhancers	Primary B cells from peripheral blood	blood
15	chr6:179800-180400	Enhancers	GM12878-XiMat	blood
16	chr6:180200-186600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:180200-190800	Enhancers	Primary B cells from cord blood	blood
18	chr6:180400-180600	Active TSS	Primary T cells from cord blood	blood
19	chr6:180400-180800	Enhancers	Fetal Thymus	thymus
20	chr6:180400-181200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr6:180400-181200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr6:180400-181400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr6:180400-181800	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr6:180400-181800	Active TSS	Thymus	Thymus
25	chr6:180400-182000	Flanking Active TSS	GM12878-XiMat	blood
26	chr6:180600-180800	Enhancers	Primary hematopoietic stem cells	blood
27	chr6:180600-181000	Flanking Active TSS	Primary T cells from cord blood	blood
28	chr6:180600-181000	Enhancers	Spleen	Spleen
29	chr6:180600-181200	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr6:180600-181400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr6:180600-181400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr6:180800-181000	Flanking Active TSS	Fetal Thymus	thymus
33	chr6:180800-181200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
34	chr6:180800-186800	Weak transcription	Primary hematopoietic stem cells	blood
35	chr6:181000-181400	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr6:181000-181400	Enhancers	Fetal Thymus	thymus
37	chr6:181000-181800	Enhancers	Primary T cells from cord blood	blood
38	chr6:181000-194800	Weak transcription	Spleen	Spleen
39	chr6:181200-183600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr6:181200-194400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr6:181400-183200	Weak transcription	Fetal Thymus	thymus
42	chr6:181400-188800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr6:181800-183600	Weak transcription	Thymus	Thymus
44	chr6:181800-184200	Weak transcription	Primary T cells from cord blood	blood
45	chr6:181800-188800	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr6:182000-184800	Enhancers	GM12878-XiMat	blood
47	chr6:183200-187800	Enhancers	Fetal Thymus	thymus
48	chr6:183600-184800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr6:183600-188000	Enhancers	Thymus	Thymus
50	chr6:184200-184600	Enhancers	Primary T cells from cord blood	blood

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