Variant report

Variant	nsv1018838
Chromosome Location	chr5:164942118-165164396
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	chr5:165057261-165057944	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:165054757-165055232	HepG2	liver:	n/a	n/a
3	ATF1	chr5:165125132-165125257	K562	blood:	n/a	n/a
4	BHLHE40	chr5:165054799-165055121	HepG2	liver:	n/a	n/a
5	BRCA1	chr5:165050042-165050169	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr5:165125639-165125761	A549	lung:	n/a	n/a
7	CEBPB	chr5:165054775-165055208	HepG2	liver:	n/a	n/a
8	CEBPB	chr5:165058379-165058524	A549	lung:	n/a	chr5:165058447-165058458
9	CEBPB	chr5:165139622-165139796	A549	lung:	n/a	n/a
10	CEBPB	chr5:165133464-165133664	HepG2	liver:	n/a	chr5:165133620-165133631
11	CEBPB	chr5:164963767-164964062	IMR90	lung:	n/a	chr5:164963881-164963894
12	CEBPB	chr5:165058340-165058501	HepG2	liver:	n/a	chr5:165058447-165058458
13	CEBPB	chr5:165058264-165058629	HepG2	liver:	n/a	chr5:165058447-165058458
14	CEBPB	chr5:165047253-165047834	IMR90	lung:	n/a	chr5:165047638-165047649 chr5:165047423-165047436
15	CEBPB	chr5:164952272-164952683	Hela-S3	cervix:	n/a	chr5:164952519-164952532 chr5:164952521-164952532 chr5:164952519-164952530
16	CEBPB	chr5:164977443-164977643	HepG2	liver:	n/a	n/a
17	CEBPB	chr5:165058275-165058647	IMR90	lung:	n/a	chr5:165058447-165058458
18	CEBPB	chr5:165043632-165043863	MCF-7	breast:	n/a	n/a
19	CEBPB	chr5:165054873-165055004	HepG2	liver:	n/a	n/a
20	CEBPB	chr5:165052569-165052903	HepG2	liver:	n/a	chr5:165052746-165052757
21	CEBPB	chr5:165050028-165050383	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr5:165052591-165052926	IMR90	lung:	n/a	chr5:165052746-165052757
23	CEBPB	chr5:165043553-165043878	IMR90	lung:	n/a	n/a
24	CEBPB	chr5:165052620-165052852	Hela-S3	cervix:	n/a	chr5:165052746-165052757
25	CEBPB	chr5:165058304-165058623	H1-hESC	embryonic stem cell:	n/a	chr5:165058447-165058458
26	CEBPB	chr5:165080111-165080228	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr5:165127615-165127816	HepG2	liver:	n/a	chr5:165127725-165127736
28	CEBPB	chr5:164952223-164952702	IMR90	lung:	n/a	chr5:164952519-164952532 chr5:164952521-164952532 chr5:164952519-164952530
29	CEBPB	chr5:165121073-165121296	HepG2	liver:	n/a	n/a
30	CEBPB	chr5:164952386-164952643	HepG2	liver:	n/a	chr5:164952519-164952532 chr5:164952521-164952532 chr5:164952519-164952530
31	CEBPB	chr5:164964623-164964942	IMR90	lung:	n/a	n/a
32	CHD2	chr5:165054924-165055124	HepG2	liver:	n/a	n/a
33	CTCF	chr5:165057022-165057718	A549	lung:	n/a	chr5:165057413-165057429 chr5:165057416-165057423 chr5:165057412-165057430 chr5:165057414-165057435 chr5:165057415-165057428
34	CTCF	chr5:165057360-165057510	GM12875	blood:	n/a	chr5:165057413-165057429 chr5:165057416-165057423 chr5:165057412-165057430 chr5:165057414-165057435 chr5:165057415-165057428
35	CTCF	chr5:165140420-165140570	GM12867	blood:	n/a	n/a
36	CTCF	chr5:165057306-165057542	HepG2	liver:	n/a	chr5:165057413-165057429 chr5:165057416-165057423 chr5:165057412-165057430 chr5:165057414-165057435 chr5:165057415-165057428
37	CTCF	chr5:165057340-165057490	AG04450	lung:	n/a	chr5:165057413-165057429 chr5:165057416-165057423 chr5:165057412-165057430 chr5:165057414-165057435 chr5:165057415-165057428
38	CTCF	chr5:165057320-165057470	Hela-S3	cervix:	n/a	chr5:165057413-165057429 chr5:165057416-165057423 chr5:165057412-165057430 chr5:165057414-165057435 chr5:165057415-165057428
39	CTCF	chr5:165043661-165043855	LNCaP	prostate:	n/a	n/a
40	CTCF	chr5:165139180-165139330	GM12866	blood:	n/a	n/a
41	CTCF	chr5:165057320-165057470	NHLF	lung:	n/a	chr5:165057413-165057429 chr5:165057416-165057423 chr5:165057412-165057430 chr5:165057414-165057435 chr5:165057415-165057428
42	CTCF	chr5:165057692-165057695	GM10266	blood:	n/a	n/a
43	CTCF	chr5:165057282-165057513	MCF-7	breast:	n/a	chr5:165057413-165057429 chr5:165057416-165057423 chr5:165057412-165057430 chr5:165057414-165057435 chr5:165057415-165057428
44	CTCF	chr5:165057340-165057490	HL-60	blood:	n/a	chr5:165057413-165057429 chr5:165057416-165057423 chr5:165057412-165057430 chr5:165057414-165057435 chr5:165057415-165057428
45	CTCF	chr5:165057340-165057490	HCPEpiC	choroid plexus:	n/a	chr5:165057413-165057429 chr5:165057416-165057423 chr5:165057412-165057430 chr5:165057414-165057435 chr5:165057415-165057428
46	CTCF	chr5:165057260-165057410	HCT-116	colon:	n/a	n/a
47	CTCF	chr5:165081628-165081660	GM20000	blood:	n/a	n/a
48	CTCF	chr5:165057360-165057510	Hela-S3	cervix:	n/a	chr5:165057413-165057429 chr5:165057416-165057423 chr5:165057412-165057430 chr5:165057414-165057435 chr5:165057415-165057428
49	CTCF	chr5:165057325-165057538	SK-N-SH_RA	brain:	n/a	chr5:165057413-165057429 chr5:165057416-165057423 chr5:165057412-165057430 chr5:165057414-165057435 chr5:165057415-165057428
50	CTCF	chr5:165057306-165057493	SK-N-SH_RA	brain:	n/a	chr5:165057413-165057429 chr5:165057416-165057423 chr5:165057412-165057430 chr5:165057414-165057435 chr5:165057415-165057428

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:165085761-165085811	Hepatocyte	liver:	n/a
2	chr5:165085761-165085811	Hepatocyte	liver:	n/a
3	chr5:165063158-165063208	RPTEC	kidney:	n/a
4	chr5:165085761-165085811	SKMC	muscle:	n/a
5	chr5:165085761-165085811	AG04449	skin:	fetal
6	chr5:165085761-165085811	AoSMC	blood vessel:	n/a
7	chr5:165085761-165085811	H1-hESC	embryonic stem cell:	embryo
8	chr5:165085761-165085811	HAEpiC	amniotic membrane:	n/a
9	chr5:165063158-165063208	MCF-7	breast:	n/a
10	chr5:165063158-165063208	A549	lung:	n/a
11	chr5:165063158-165063208	HepG2	liver:	n/a
12	chr5:165063158-165063208	Caco-2	colon:	n/a
13	chr5:165063158-165063208	HCPEpiC	choroid plexus:	n/a
14	chr5:165063158-165063208	HMEC	breast:	n/a
15	chr5:165085761-165085811	Jurkat	blood:	n/a
16	chr5:165063158-165063208	SK-N-SH	brain:	n/a
17	chr5:165085761-165085811	Hela-S3	cervix:	n/a
18	chr5:165085761-165085811	HepG2	liver:	n/a
19	chr5:165085761-165085811	HCPEpiC	choroid plexus:	n/a
20	chr5:165063158-165063208	GM12878	blood:	n/a
21	chr5:165063158-165063208	H1-hESC	embryonic stem cell:	embryo
22	chr5:165085761-165085811	GM12892	blood:	n/a
23	chr5:165063158-165063208	HEK293	kidney:	embryo
24	chr5:165063158-165063208	T-47D	breast:	n/a
25	chr5:165085761-165085811	GM12891	blood:	n/a
26	chr5:165085761-165085811	HEEpiC	esophagus:	n/a
27	chr5:165063158-165063208	AG10803	skin:	n/a
28	chr5:165085761-165085811	HEK293	kidney:	embryo
29	chr5:165063158-165063208	AG09309	skin:	n/a
30	chr5:165085761-165085811	K562	blood:	n/a
31	chr5:165085761-165085811	HNPCEpiC	eye:	n/a
32	chr5:165085761-165085811	T-47D	breast:	n/a
33	chr5:165063158-165063208	GM12891	blood:	n/a
34	chr5:165063158-165063208	NH-A	brain:	n/a
35	chr5:165063158-165063208	AG04450	lung:	fetal
36	chr5:165063158-165063208	SK-N-SH_RA	brain:	n/a
37	chr5:165063158-165063208	PrEC	prostate:	n/a
38	chr5:165085761-165085811	CMK	blood:	n/a
39	chr5:165085761-165085811	Caco-2	colon:	n/a
40	chr5:165085761-165085811	NB4	blood:	n/a
41	chr5:165063158-165063208	HCT-116	colon:	n/a
42	chr5:165063158-165063208	PANC-1	pancreas:	n/a
43	chr5:165063158-165063208	HAEpiC	amniotic membrane:	n/a
44	chr5:165085761-165085811	BE2_C	brain:	n/a
45	chr5:165085761-165085811	AG09319	gingival:	n/a
46	chr5:165063158-165063208	SK-N-MC	brain:	n/a
47	chr5:165085761-165085811	AG04450	lung:	fetal
48	chr5:165063158-165063208	HRE	kidney:	n/a
49	chr5:165063158-165063208	Hepatocyte	liver:	n/a
50	chr5:165063158-165063208	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr5:165057168..165057830-chr5:166127299..166127876,2	MCF-7	breast:
2	chr5:165056998..165057856-chr5:165307984..165308755,4	MCF-7	breast:
3	chr5:165051988..165053700-chr5:165055288..165056813,2	K562	blood:
4	chr5:165056748..165057320-chr5:166502236..166502910,2	MCF-7	breast:
5	chr5:164942492..164944105-chr5:164947247..164948752,2	K562	blood:
6	chr5:165002408..165004475-chr5:165008140..165010199,2	K562	blood:
7	chr5:165006519..165009278-chr5:168004654..168006646,2	K562	blood:
8	chr5:165051988..165053700-chr5:165055288..165056813,2	K562	blood:
9	chr5:164947556..164949142-chr5:164952673..164954604,2	MCF-7	breast:
10	chr5:164942492..164944105-chr5:164947247..164948752,2	K562	blood:
11	chr5:164999543..165002349-chr5:165008239..165011140,2	MCF-7	breast:
12	chr5:164947556..164949142-chr5:164952673..164954604,2	MCF-7	breast:
13	chr5:164999543..165002349-chr5:165008239..165011140,2	MCF-7	breast:
14	chr5:165002408..165004475-chr5:165008140..165010199,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ODZ2-4	chr5:165036446-165036684	NONHSAT104956

Variant related genes	Relation type
RN7SKP60	TF binding region
RN7SKP60	CpG island
ENSG00000120137	chromatin interactions

Extended variants
information (count: 3745 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:3745 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549590801	chr5:164948643-164948644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs377741112	chr5:164948645-164948646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561049682	chr5:164948650-164948651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531262981	chr5:164948688-164948689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78966709	chr5:164948729-164948730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571122107	chr5:164948771-164948772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs9314071	chr5:164948823-164948824	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs547334004	chr5:164948851-164948852	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs565627082	chr5:164948868-164948869	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs66488381	chr5:164948869-164948870	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs189937928	chr5:164948871-164948872	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs148426520	chr5:164948919-164948920	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs373312500	chr5:164948933-164948934	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs556602902	chr5:164948936-164948937	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs182119053	chr5:164949000-164949001	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs576586739	chr5:164949026-164949027	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs545419073	chr5:164949063-164949064	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs142428041	chr5:164949081-164949082	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs111906784	chr5:164949109-164949110	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs114429024	chr5:164949135-164949136	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs543487690	chr5:164949252-164949253	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs34495179	chr5:164949300-164949301	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs201607128	chr5:164949321-164949322	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs2431175	chr5:164949332-164949333	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs58862578	chr5:164949333-164949334	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs561296399	chr5:164949379-164949380	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs575723610	chr5:164949396-164949397	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs186508165	chr5:164949397-164949398	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs564989443	chr5:164949432-164949433	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs544365789	chr5:164949441-164949442	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs114904223	chr5:164949550-164949551	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs200453818	chr5:164949555-164949556	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs546947560	chr5:164949559-164949560	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs565639106	chr5:164949631-164949632	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs529907599	chr5:164949651-164949652	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs191408793	chr5:164949674-164949675	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs569781546	chr5:164949699-164949700	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs151294239	chr5:164949713-164949714	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs556430836	chr5:164949734-164949735	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs75630968	chr5:164949765-164949766	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs572030069	chr5:164949767-164949768	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs115510986	chr5:164949800-164949801	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs143597946	chr5:164951812-164951813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185305792	chr5:164951826-164951827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114506503	chr5:164951828-164951829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs35694368	chr5:164951859-164951860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542417023	chr5:164951879-164951880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115152794	chr5:164951883-164951884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs6869930	chr5:164951897-164951898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560762859	chr5:164951911-164951912	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	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
Breast cancer	21858162	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
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	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
Breast cancer	17603634	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
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
severe myoclonic epilepsy of infancy	18294202	CNVD
Olfactory neuroblastoma	18408657	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:164948600-164949000	Enhancers	Colon Smooth Muscle	Colon
2	chr5:164948600-164949000	Enhancers	Rectal Smooth Muscle	rectum
3	chr5:164948600-164949800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr5:164948800-164949000	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr5:164948800-164949000	Flanking Active TSS	Fetal Lung	lung
6	chr5:164948800-164949400	Active TSS	Rectal Mucosa Donor 29	rectum
7	chr5:164948800-164949600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr5:164949000-164949600	Active TSS	Brain Inferior Temporal Lobe	brain
9	chr5:164949000-164949800	Active TSS	Fetal Lung	lung
10	chr5:164951800-164952800	Enhancers	Placenta Amnion	Placenta Amnion
11	chr5:164952000-164952600	Enhancers	Placenta	Placenta
12	chr5:164952600-164953000	Enhancers	NHLF	lung
13	chr5:164952800-164953400	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr5:164953600-164953800	Enhancers	Placenta Amnion	Placenta Amnion
15	chr5:164955000-164955400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:164955400-164955800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:164964200-164965800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr5:164964800-164965200	Enhancers	Rectal Smooth Muscle	rectum
19	chr5:164965200-164968600	Weak transcription	Rectal Smooth Muscle	rectum
20	chr5:164968000-164968200	Active TSS	Gastric	stomach
21	chr5:164978800-164980200	Enhancers	Fetal Lung	lung
22	chr5:164979200-164979600	Enhancers	Ovary	ovary
23	chr5:164986200-164986800	Enhancers	Primary B cells from cord blood	blood
24	chr5:164986200-164987200	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr5:164986200-164988200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr5:164986400-164987400	Enhancers	Primary hematopoietic stem cells	blood
27	chr5:164986600-164987000	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr5:164986600-164987200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr5:164986600-164987200	Enhancers	Dnd41	blood
30	chr5:164986600-164987400	Enhancers	Primary B cells from peripheral blood	blood
31	chr5:164986800-164988000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr5:164986800-164988000	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr5:164987000-164987800	Enhancers	Fetal Brain Male	brain
34	chr5:164987800-164988000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr5:164987800-164988000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr5:164987800-164988200	Enhancers	Fetal Brain Female	brain
37	chr5:164988000-164992800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:164988000-164993000	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr5:164990000-164990800	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr5:164990000-164990800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr5:164990200-164990800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:164990400-164990800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr5:164990400-164990800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr5:164990400-164991000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr5:164990600-164990800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr5:164990800-164992200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr5:164990800-164992600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr5:164992200-164993200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr5:164992600-164993200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr5:164992600-164994000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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