Variant report

Variant	nsv1016614
Chromosome Location	chr5:180163353-180216254
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	ATF2	chr5:180212570-180213141	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr5:180212679-180213244	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr5:180169789-180169977	GM12878	blood:	n/a	n/a
4	CBX3	chr5:180208858-180209504	K562	blood:	n/a	n/a
5	CBX3	chr5:180198766-180199290	K562	blood:	n/a	n/a
6	CBX3	chr5:180198844-180199194	K562	blood:	n/a	n/a
7	CBX3	chr5:180208965-180209392	K562	blood:	n/a	n/a
8	CBX3	chr5:180215613-180215981	K562	blood:	n/a	n/a
9	CEBPB	chr5:180209005-180209250	K562	blood:	n/a	n/a
10	CEBPB	chr5:180208882-180209430	K562	blood:	n/a	n/a
11	CEBPD	chr5:180208780-180209396	K562	blood:	n/a	n/a
12	CEBPD	chr5:180208777-180209303	K562	blood:	n/a	n/a
13	CTCF	chr5:180211600-180211750	GM12873	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
14	CTCF	chr5:180211620-180211770	AoAF	blood vessel:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
15	CTCF	chr5:180211569-180211810	K562	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
16	CTCF	chr5:180211580-180211730	GM12872	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
17	CTCF	chr5:180211600-180211750	GM12874	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
18	CTCF	chr5:180211555-180211820	GM13977	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
19	CTCF	chr5:180211572-180211814	Kidney_OC	kidney:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
20	CTCF	chr5:180214160-180214310	AG09309	skin:	n/a	n/a
21	CTCF	chr5:180216060-180216210	NHDF-neo	bronchial:	n/a	n/a
22	CTCF	chr5:180211580-180211730	HCT-116	colon:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
23	CTCF	chr5:180214300-180214450	AoAF	blood vessel:	n/a	chr5:180214351-180214360
24	CTCF	chr5:180211640-180211790	NB4	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
25	CTCF	chr5:180211544-180211827	LNCaP	prostate:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
26	CTCF	chr5:180211555-180211834	HUVEC	blood vessel:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
27	CTCF	chr5:180211600-180211750	HepG2	liver:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
28	CTCF	chr5:180214240-180214390	AG10803	skin:	n/a	chr5:180214351-180214360
29	CTCF	chr5:180211600-180211750	MCF-7	breast:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
30	CTCF	chr5:180211580-180211730	GM12874	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
31	CTCF	chr5:180211580-180211730	GM12868	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
32	CTCF	chr5:180211580-180211730	GM12866	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
33	CTCF	chr5:180211564-180211813	MCF-7	breast:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
34	CTCF	chr5:180211620-180211770	HBMEC	blood vessel:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
35	CTCF	chr5:180211640-180211790	K562	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
36	CTCF	chr5:180211620-180211770	HEEpiC	esophagus:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
37	CTCF	chr5:180211180-180211330	HMEC	breast:	n/a	n/a
38	CTCF	chr5:180211540-180211690	HCM	heart:	n/a	n/a
39	CTCF	chr5:180211620-180211770	AG04450	lung:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
40	CTCF	chr5:180211580-180211730	GM12878	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
41	CTCF	chr5:180214900-180215050	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr5:180211455-180211919	A549	lung:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
43	CTCF	chr5:180214322-180214360	H1-hESC	embryonic stem cell:	n/a	chr5:180214351-180214360
44	CTCF	chr5:180214160-180214310	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr5:180211552-180211830	GM19238	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
46	CTCF	chr5:180211620-180211770	HRE	kidney:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
47	CTCF	chr5:180212320-180212470	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr5:180211395-180211982	MCF-7	breast:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
49	CTCF	chr5:180214140-180214290	HCFaa	heart:	n/a	n/a
50	CTCF	chr5:180216160-180216310	NHDF-neo	bronchial:	n/a	chr5:180216211-180216232 chr5:180216214-180216235 chr5:180216219-180216237

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:180166492-180166542	SK-N-SH_RA	brain:	n/a
2	chr5:180213189-180213239	MCF-7	breast:	n/a
3	chr5:180166492-180166542	GM12878	blood:	n/a
4	chr5:180167566-180167616	MCF10A-Er-Src	breast:	n/a
5	chr5:180167965-180168015	NHBE	bronchial:	n/a
6	chr5:180167724-180167774	MCF-7	breast:	n/a
7	chr5:180167566-180167616	NB4	blood:	n/a
8	chr5:180167724-180167774	MCF10A-Er-Src	breast:	n/a
9	chr5:180167132-180167182	HRE	kidney:	n/a
10	chr5:180167566-180167616	HRPEpiC	eye:	n/a
11	chr5:180166492-180166542	SKMC	muscle:	n/a
12	chr5:180166492-180166542	PANC-1	pancreas:	n/a
13	chr5:180167566-180167616	BE2_C	brain:	n/a
14	chr5:180167566-180167616	HCT-116	colon:	n/a
15	chr5:180167965-180168015	HCPEpiC	choroid plexus:	n/a
16	chr5:180166492-180166542	HAEpiC	amniotic membrane:	n/a
17	chr5:180167132-180167182	SK-N-SH	brain:	n/a
18	chr5:180166694-180166744	AG04449	skin:	fetal
19	chr5:180167566-180167616	AG04450	lung:	fetal
20	chr5:180167724-180167774	BJ	skin:	n/a
21	chr5:180167566-180167616	NHBE	bronchial:	n/a
22	chr5:180167724-180167774	K562	blood:	n/a
23	chr5:180213189-180213239	K562	blood:	n/a
24	chr5:180167724-180167774	AG04450	lung:	fetal
25	chr5:180166694-180166744	MCF-7	breast:	n/a
26	chr5:180167965-180168015	GM12892	blood:	n/a
27	chr5:180166694-180166744	HMEC	breast:	n/a
28	chr5:180166694-180166744	SK-N-SH	brain:	n/a
29	chr5:180213189-180213239	Hela-S3	cervix:	n/a
30	chr5:180213189-180213239	HCPEpiC	choroid plexus:	n/a
31	chr5:180167132-180167182	HMEC	breast:	n/a
32	chr5:180167965-180168015	HCT-116	colon:	n/a
33	chr5:180166492-180166542	A549	lung:	n/a
34	chr5:180213189-180213239	HNPCEpiC	eye:	n/a
35	chr5:180167965-180168015	NT2-D1	testis:	n/a
36	chr5:180167724-180167774	HIPEpiC	eye:	n/a
37	chr5:180167724-180167774	HCT-116	colon:	n/a
38	chr5:180213189-180213239	SKMC	muscle:	n/a
39	chr5:180166694-180166744	H1-hESC	embryonic stem cell:	embryo
40	chr5:180167965-180168015	RPTEC	kidney:	n/a
41	chr5:180213189-180213239	NT2-D1	testis:	n/a
42	chr5:180166492-180166542	NH-A	brain:	n/a
43	chr5:180166694-180166744	AG10803	skin:	n/a
44	chr5:180166694-180166744	HCM	heart:	n/a
45	chr5:180167724-180167774	HCM	heart:	n/a
46	chr5:180213189-180213239	HRCEpiC	kidney:	n/a
47	chr5:180167965-180168015	GM06990	blood:	n/a
48	chr5:180166492-180166542	RPTEC	kidney:	n/a
49	chr5:180166694-180166744	PrEC	prostate:	n/a
50	chr5:180166694-180166744	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:180208930..180211085-chr5:180226767..180229407,2	K562	blood:
2	chr5:180208714..180211260-chr5:180212096..180214924,3	K562	blood:
3	chr5:180208714..180211702-chr5:180212096..180213803,2	K562	blood:
4	chr5:180207628..180210924-chr5:180228309..180230947,5	MCF-7	breast:
5	chr5:180202113..180204208-chr5:180208493..180210882,2	K562	blood:
6	chr5:180168390..180170515-chr5:180204872..180207367,2	K562	blood:
7	chr5:180158275..180159905-chr5:180163258..180165205,2	K562	blood:
8	chr5:180202321..180205166-chr5:180643152..180645917,2	K562	blood:
9	chr5:180211281..180211887-chr5:180586366..180586939,2	MCF-7	breast:
10	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
11	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
12	chr5:180209019..180210957-chr5:180453882..180456380,2	K562	blood:
13	chr5:180207548..180210211-chr5:180589188..180591545,3	K562	blood:
14	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
15	chr5:180208714..180211702-chr5:180212096..180213803,2	K562	blood:
16	chr5:180210430..180214631-chr5:180286463..180290673,6	MCF-7	breast:
17	chr5:180202113..180204208-chr5:180208493..180210882,2	K562	blood:
18	chr5:180211640..180213961-chr5:180214094..180219248,5	K562	blood:
19	chr5:180211375..180212214-chr5:180226180..180226854,2	MCF-7	breast:
20	chr5:180211185..180212156-chr5:180225940..180226892,9	MCF-7	breast:
21	chr5:180212092..180214294-chr5:180453988..180456472,2	K562	blood:
22	chr5:180170663..180173512-chr5:180175093..180176860,2	K562	blood:
23	chr5:180170663..180173512-chr5:180175093..180176860,2	K562	blood:
24	chr5:179919075..179921338-chr5:180210769..180213087,2	MCF-7	breast:
25	chr5:180168390..180170515-chr5:180204872..180207367,2	K562	blood:
26	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
27	chr5:180172009..180174376-chr5:180240608..180243076,2	MCF-7	breast:
28	chr5:180210073..180212750-chr5:180649135..180651698,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTNL8-8	chr5:180193918-180195284	ucscGeneNc_uc003mmk_2
2	lnc-BTNL8-8	chr5:180190563-180190835	ucscGeneNc_uc003mmk_2
3	lnc-BTNL8-8	chr5:180192279-180192466	ucscGeneNc_uc003mmk_2
4	lnc-OR2Y1-2	chr5:180189565-180191201	ucscGeneNc_uc003mmj_1

Variant related genes	Relation type
ENSG00000260841	TF binding region
OR2Y1	TF binding region
ENSG00000260841	CpG island
OR2Y1	CpG island
ENSG00000264732	chromatin interactions
ENSG00000131446	chromatin interactions
ENSG00000196670	chromatin interactions
ENSG00000260841	chromatin interactions
ENSG00000146063	chromatin interactions

Extended variants
information (count: 1160 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140068130	chr5:180165250-180165251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs150380939	chr5:180165251-180165252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549503851	chr5:180165308-180165309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569730796	chr5:180165341-180165342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185975066	chr5:180165352-180165353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577597806	chr5:180165353-180165354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113197425	chr5:180165358-180165359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10479581	chr5:180165367-180165368	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs534891067	chr5:180165391-180165392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558062269	chr5:180165420-180165421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs17702375	chr5:180165435-180165436	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs75506254	chr5:180165507-180165508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557491972	chr5:180165523-180165524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs17080555	chr5:180165553-180165554	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs560215918	chr5:180165597-180165598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565830273	chr5:180165616-180165617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542867424	chr5:180165677-180165678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs578255984	chr5:180165701-180165702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113971523	chr5:180165704-180165705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191990860	chr5:180165705-180165706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184011760	chr5:180165706-180165707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7737219	chr5:180165743-180165744	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs565227639	chr5:180165748-180165749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537707432	chr5:180165749-180165750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532812624	chr5:180165811-180165812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149093343	chr5:180165841-180165842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569663250	chr5:180165855-180165856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528951033	chr5:180165860-180165861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188561856	chr5:180165870-180165871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370478662	chr5:180165886-180165887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565895688	chr5:180165933-180165934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574038591	chr5:180165946-180165947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551741196	chr5:180165975-180165976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150261063	chr5:180165976-180165977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375326413	chr5:180165979-180165980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs386695804	chr5:180165983-180165984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190409241	chr5:180165985-180165986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574072159	chr5:180165993-180165994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182642981	chr5:180166017-180166018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536776990	chr5:180166018-180166019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543376755	chr5:180166074-180166075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375740992	chr5:180166104-180166105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370033340	chr5:180166106-180166107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201325186	chr5:180166120-180166121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145162555	chr5:180166126-180166127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144773749	chr5:180166140-180166141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9329115	chr5:180166141-180166142	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs61737057	chr5:180166164-180166165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575495208	chr5:180166173-180166174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs61735555	chr5:180166256-180166257	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	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
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	17440070	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:180165200-180170800	Weak transcription	Right Atrium	heart
2	chr5:180166600-180166800	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:180166600-180167600	Enhancers	HSMMtube	muscle
4	chr5:180169800-180170000	Bivalent Enhancer	K562	blood
5	chr5:180196600-180197200	Enhancers	HepG2	liver
6	chr5:180202000-180202800	Enhancers	K562	blood
7	chr5:180202800-180203000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:180202800-180206000	Weak transcription	K562	blood
9	chr5:180203000-180212400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:180204400-180215400	Weak transcription	Primary B cells from cord blood	blood
11	chr5:180205200-180209800	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr5:180205600-180211800	Weak transcription	Liver	Liver
13	chr5:180205800-180212400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr5:180206000-180208400	Enhancers	K562	blood
15	chr5:180206000-180212200	Weak transcription	Lung	lung
16	chr5:180206200-180209800	Weak transcription	Primary T cells from cord blood	blood
17	chr5:180206600-180212400	Weak transcription	Aorta	Aorta
18	chr5:180206800-180210800	Weak transcription	Esophagus	oesophagus
19	chr5:180207000-180207200	Enhancers	Right Atrium	heart
20	chr5:180207000-180214600	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr5:180207200-180212200	Weak transcription	Right Atrium	heart
22	chr5:180207200-180212400	Weak transcription	Fetal Intestine Large	intestine
23	chr5:180207800-180210800	Weak transcription	Placenta	Placenta
24	chr5:180208000-180212000	Weak transcription	Stomach Smooth Muscle	stomach
25	chr5:180208000-180212400	Weak transcription	Psoas Muscle	Psoas
26	chr5:180208400-180208600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr5:180208400-180210000	Flanking Active TSS	K562	blood
28	chr5:180209200-180214000	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr5:180209200-180214800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr5:180209400-180209800	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr5:180209400-180209800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr5:180209400-180210200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr5:180209600-180210000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr5:180209600-180210000	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr5:180209600-180210200	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr5:180209600-180210400	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr5:180209800-180210400	Enhancers	Primary T cells from cord blood	blood
38	chr5:180209800-180211000	Enhancers	Primary T cells fromperipheralblood	blood
39	chr5:180209800-180212200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr5:180209800-180213200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr5:180210000-180210200	Enhancers	Colon Smooth Muscle	Colon
42	chr5:180210000-180210400	Enhancers	Thymus	Thymus
43	chr5:180210000-180211200	Enhancers	K562	blood
44	chr5:180210000-180214000	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr5:180210000-180217800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr5:180210200-180210400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr5:180210200-180210600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr5:180210200-180211200	Enhancers	Fetal Thymus	thymus
49	chr5:180210200-180212400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr5:180210200-180212400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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