Variant report

Variant	nsv969027
Chromosome Location	chr5:179061852-179079829
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:135)
CpG islands
(count:366)
Chromatin interactive
region (count:11)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:135 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr5:179075535-179075759	HepG2	liver:	n/a	n/a
2	BHLHE40	chr5:179075505-179075756	K562	blood:	n/a	n/a
3	CBX3	chr5:179061169-179062060	K562	blood:	n/a	n/a
4	CBX3	chr5:179061364-179061876	K562	blood:	n/a	n/a
5	CTCF	chr5:179061369-179061929	GM12892	blood:	n/a	n/a
6	CTCF	chr5:179061915-179061930	GM19240	blood:	n/a	n/a
7	CTCF	chr5:179061740-179061880	GM10248	blood:	n/a	n/a
8	CTCF	chr5:179078140-179078290	NHDF-neo	bronchial:	n/a	chr5:179078192-179078210
9	CTCF	chr5:179070085-179070198	GM10266	blood:	n/a	n/a
10	CTCF	chr5:179070105-179070183	GM13976	blood:	n/a	n/a
11	CTCF	chr5:179070108-179070207	LNCaP	prostate:	n/a	n/a
12	CTCF	chr5:179061793-179061939	GM19238	blood:	n/a	n/a
13	CTCF	chr5:179061775-179061864	GM19240	blood:	n/a	n/a
14	CTCF	chr5:179074854-179074891	GM10266	blood:	n/a	n/a
15	CTCF	chr5:179061845-179061890	GM10266	blood:	n/a	n/a
16	CTCF	chr5:179068060-179068210	Caco-2	colon:	n/a	n/a
17	CTCF	chr5:179062030-179062116	GM10266	blood:	n/a	n/a
18	CTCF	chr5:179061919-179061943	GM12891	blood:	n/a	n/a
19	CTCF	chr5:179063284-179063355	GM10248	blood:	n/a	n/a
20	CTCF	chr5:179061209-179061923	K562	blood:	n/a	n/a
21	CTCF	chr5:179063251-179063304	Pancreas_OC	pancreas:	n/a	n/a
22	CTCF	chr5:179061784-179061951	GM12878	blood:	n/a	n/a
23	CTCF	chr5:179076103-179076173	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr5:179079568-179079625	LNCaP	prostate:	n/a	n/a
25	CTCF	chr5:179061909-179061914	GM12891	blood:	n/a	n/a
26	CTCF	chr5:179061824-179061879	K562	blood:	n/a	n/a
27	CTCF	chr5:179078632-179078674	Medullo	brain:	n/a	n/a
28	E2F6	chr5:179076683-179076795	K562	blood:	n/a	n/a
29	ELF1	chr5:179076235-179076491	K562	blood:	n/a	chr5:179076372-179076385
30	FOSL2	chr5:179061003-179061897	HepG2	liver:	n/a	n/a
31	FOSL2	chr5:179068829-179069083	HepG2	liver:	n/a	n/a
32	FOSL2	chr5:179079667-179079921	HepG2	liver:	n/a	chr5:179079860-179079871 chr5:179079861-179079869
33	FOXA1	chr5:179075948-179076171	HepG2	liver:	n/a	chr5:179076077-179076089
34	FOXP2	chr5:179061646-179061862	PFSK-1	brain:	n/a	n/a
35	FOXP2	chr5:179061902-179062181	PFSK-1	brain:	n/a	n/a
36	GABPA	chr5:179061664-179062143	HepG2	liver:	n/a	n/a
37	GABPA	chr5:179061650-179061864	HepG2	liver:	n/a	n/a
38	GABPA	chr5:179061635-179061866	K562	blood:	n/a	n/a
39	GATA2	chr5:179061322-179061998	K562	blood:	n/a	chr5:179061334-179061342
40	HEY1	chr5:179061198-179062005	K562	blood:	n/a	chr5:179061213-179061228 chr5:179061480-179061495
41	HEY1	chr5:179061438-179061853	HepG2	liver:	n/a	chr5:179061480-179061495
42	HEY1	chr5:179061148-179062048	K562	blood:	n/a	chr5:179061213-179061228 chr5:179061480-179061495
43	HEY1	chr5:179061160-179062054	HepG2	liver:	n/a	chr5:179061213-179061228 chr5:179061480-179061495
44	IRF4	chr5:179061136-179062077	GM12878	blood:	n/a	n/a
45	MAX	chr5:179075469-179075831	K562	blood:	n/a	chr5:179075657-179075668 chr5:179075657-179075667 chr5:179075658-179075667 chr5:179075657-179075668 chr5:179075656-179075669 chr5:179075656-179075671
46	MAX	chr5:179075543-179075763	K562	blood:	n/a	chr5:179075657-179075668 chr5:179075657-179075667 chr5:179075658-179075667 chr5:179075657-179075668 chr5:179075656-179075669 chr5:179075656-179075671
47	MYC	chr5:179061921-179061975	MCF-7	breast:	n/a	n/a
48	MYC	chr5:179061728-179061942	K562	blood:	n/a	n/a
49	MYC	chr5:179061018-179062152	MCF-7	breast:	n/a	n/a
50	MYC	chr5:179061731-179061869	GM12878	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179075765-179075815	PFSK-1	brain:	n/a
2	chr5:179069308-179069358	AG09319	gingival:	n/a
3	chr5:179075765-179075815	ECC-1	luminal epithelium:	n/a
4	chr5:179075765-179075815	HRPEpiC	eye:	n/a
5	chr5:179071901-179071951	U87	brain:	n/a
6	chr5:179072247-179072297	HCT-116	colon:	n/a
7	chr5:179075765-179075815	PrEC	prostate:	n/a
8	chr5:179069308-179069358	HCPEpiC	choroid plexus:	n/a
9	chr5:179071901-179071951	AG04449	skin:	fetal
10	chr5:179075765-179075815	HIPEpiC	eye:	n/a
11	chr5:179072247-179072297	HMEC	breast:	n/a
12	chr5:179072247-179072297	RPTEC	kidney:	n/a
13	chr5:179072247-179072297	AG09319	gingival:	n/a
14	chr5:179072247-179072297	H1-hESC	embryonic stem cell:	embryo
15	chr5:179072791-179072841	GM12878	blood:	n/a
16	chr5:179071604-179071654	SAEC	small airway:	n/a
17	chr5:179075765-179075815	Hepatocyte	liver:	n/a
18	chr5:179071901-179071951	BE2_C	brain:	n/a
19	chr5:179072791-179072841	NH-A	brain:	n/a
20	chr5:179071901-179071951	Hepatocyte	liver:	n/a
21	chr5:179072791-179072841	NHDF-neo	bronchial:	n/a
22	chr5:179071901-179071951	ECC-1	luminal epithelium:	n/a
23	chr5:179071604-179071654	HUVEC	blood vessel:	n/a
24	chr5:179075765-179075815	ProgFib	skin:	n/a
25	chr5:179072791-179072841	H1-hESC	embryonic stem cell:	embryo
26	chr5:179075765-179075815	HL-60	blood:	n/a
27	chr5:179072247-179072297	AG09309	skin:	n/a
28	chr5:179071901-179071951	PFSK-1	brain:	n/a
29	chr5:179071901-179071951	HepG2	liver:	n/a
30	chr5:179072247-179072297	SK-N-SH_RA	brain:	n/a
31	chr5:179072247-179072297	NH-A	brain:	n/a
32	chr5:179075765-179075815	A549	lung:	n/a
33	chr5:179072247-179072297	T-47D	breast:	n/a
34	chr5:179071604-179071654	MCF-7	breast:	n/a
35	chr5:179072791-179072841	SK-N-MC	brain:	n/a
36	chr5:179071604-179071654	Hepatocyte	liver:	n/a
37	chr5:179071901-179071951	NH-A	brain:	n/a
38	chr5:179071604-179071654	HL-60	blood:	n/a
39	chr5:179071604-179071654	AoSMC	blood vessel:	n/a
40	chr5:179075765-179075815	HepG2	liver:	n/a
41	chr5:179072791-179072841	HRPEpiC	eye:	n/a
42	chr5:179071604-179071654	HAEpiC	amniotic membrane:	n/a
43	chr5:179072247-179072297	ovcar-3	ovarian:	n/a
44	chr5:179072247-179072297	Caco-2	colon:	n/a
45	chr5:179072247-179072297	IMR90	lung:	fetal
46	chr5:179075765-179075815	HCF	heart:	n/a
47	chr5:179072791-179072841	T-47D	breast:	n/a
48	chr5:179071604-179071654	Caco-2	colon:	n/a
49	chr5:179072247-179072297	HL-60	blood:	n/a
50	chr5:179071901-179071951	GM06990	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:179049252..179051807-chr5:179078099..179079783,3	MCF-7	breast:
2	chr5:179065572..179067135-chr5:179078949..179080962,2	K562	blood:
3	chr5:179048537..179052008-chr5:179078753..179080980,4	K562	blood:
4	chr5:179048281..179049857-chr5:179068285..179070728,2	K562	blood:
5	chr5:179048357..179051414-chr5:179069051..179070806,3	K562	blood:
6	chr5:179064378..179067657-chr5:179095247..179097749,4	K562	blood:
7	chr5:179065572..179067135-chr5:179078949..179080962,2	K562	blood:
8	chr5:179049252..179052008-chr5:179078855..179080395,2	K562	blood:
9	chr5:178976725..178979261-chr5:179073948..179076733,2	MCF-7	breast:
10	chr5:179049010..179052109-chr5:179075423..179078137,6	MCF-7	breast:
11	chr5:179048380..179051829-chr5:179074872..179077735,3	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf60-1	chr5:179068545-179070211	NONHSAT105606
2	lnc-C5orf60-1	chr5:179070431-179072008	NONHSAT105606
3	lnc-C5orf60-1	chr5:179071946-179072008	NONHSAT105608
4	lnc-C5orf60-1	chr5:179071030-179071087	NONHSAT105607
5	lnc-C5orf60-1	chr5:179070431-179070491	NONHSAT105607
6	lnc-C5orf60-1	chr5:179071332-179071842	NONHSAT105608
7	lnc-C5orf60-1	chr5:179069896-179070211	NONHSAT105607
8	lnc-C5orf60-1	chr5:179071946-179072008	NONHSAT105607

No data

Variant related genes	Relation type
ENSG00000250999	TF binding region
C5orf60	TF binding region
ENSG00000228259	TF binding region
HNRNPH1	TF binding region
ENSG00000250999	CpG island
C5orf60	CpG island
ENSG00000228259	CpG island
HNRNPH1	CpG island
ENSG00000169045	chromatin interactions
ENSG00000176783	chromatin interactions

Extended variants
information (count: 802 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:802 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368371767	chr5:179061888-179061889	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs371407874	chr5:179062667-179062668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7444944	chr5:179062902-179062903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113766661	chr5:179062987-179062988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199886620	chr5:179063187-179063188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372643737	chr5:179063287-179063288	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs62392799	chr5:179063425-179063426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200777216	chr5:179063871-179063872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs78839471	chr5:179063901-179063902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200618352	chr5:179063956-179063957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566054679	chr5:179063991-179063992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200845050	chr5:179064079-179064080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189503510	chr5:179064080-179064081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113822237	chr5:179064125-179064126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370817816	chr5:179064130-179064131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374138626	chr5:179064143-179064144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569900369	chr5:179064174-179064175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78808226	chr5:179064211-179064212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76011332	chr5:179064213-179064214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs4311396	chr5:179064233-179064234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs72662125	chr5:179064254-179064255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs55692357	chr5:179064277-179064278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144383413	chr5:179064286-179064287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72662124	chr5:179064309-179064310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs72662123	chr5:179064316-179064317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs180692513	chr5:179064322-179064323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552679648	chr5:179064332-179064333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577204584	chr5:179064334-179064335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs72662122	chr5:179064339-179064340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs72662121	chr5:179064344-179064345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs72662120	chr5:179064347-179064348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs72662119	chr5:179064352-179064353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs72662118	chr5:179064360-179064361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs80340255	chr5:179064364-179064365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370586802	chr5:179064365-179064366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs72662117	chr5:179064398-179064399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72662116	chr5:179064406-179064407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544649518	chr5:179064444-179064445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs72662115	chr5:179064460-179064461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564390466	chr5:179064475-179064476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs72662114	chr5:179064479-179064480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs72662113	chr5:179064492-179064493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187569636	chr5:179064574-179064575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543961499	chr5:179064585-179064586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548165718	chr5:179064604-179064605	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs116815766	chr5:179064769-179064770	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs529516878	chr5:179064779-179064780	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs375826021	chr5:179064785-179064786	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs191851910	chr5:179064808-179064809	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs368711741	chr5:179064859-179064860	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Acute lymphoblastic leukemia	20435627	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
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
small cell lung cancer	20016488	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179052200-179085400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:179059400-179062000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr5:179060600-179062000	Enhancers	Primary T cells fromperipheralblood	blood
4	chr5:179060600-179062000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr5:179060600-179062000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr5:179060600-179062000	Active TSS	HSMM	muscle
7	chr5:179060800-179062000	Active TSS	HUES64 Cell Line	embryonic stem cell
8	chr5:179060800-179062000	Active TSS	iPS-15b Cell Line	embryonic stem cell
9	chr5:179060800-179062000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:179060800-179065200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr5:179061000-179064600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:179061200-179062000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr5:179061200-179062000	Active TSS	Adipose Nuclei	Adipose
14	chr5:179061200-179062800	Weak transcription	Right Atrium	heart
15	chr5:179061200-179064800	Weak transcription	NHEK	skin
16	chr5:179061200-179065800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr5:179061800-179062000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr5:179061800-179062000	Enhancers	Fetal Thymus	thymus
19	chr5:179061800-179062000	Enhancers	Dnd41	blood
20	chr5:179061800-179062000	Enhancers	K562	blood
21	chr5:179062000-179064600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr5:179064600-179064800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr5:179064600-179065000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr5:179064800-179065000	Enhancers	NHEK	skin
25	chr5:179064800-179065600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr5:179065000-179065800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr5:179065000-179066600	Weak transcription	NHEK	skin
28	chr5:179065200-179065400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr5:179065600-179065800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:179065800-179066000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr5:179065800-179067000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr5:179065800-179070600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr5:179066000-179066400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr5:179066400-179066800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr5:179066600-179066800	Enhancers	NHEK	skin
36	chr5:179070000-179070600	Active TSS	Spleen	Spleen
37	chr5:179070200-179071000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr5:179070600-179070800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr5:179070800-179078000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr5:179071800-179072400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:179075400-179075800	Enhancers	Fetal Muscle Leg	muscle
42	chr5:179075400-179076800	Enhancers	Fetal Muscle Trunk	muscle
43	chr5:179076200-179076600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr5:179076200-179076800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr5:179076400-179076600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr5:179078000-179078200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr5:179078000-179078400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr5:179078000-179078400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr5:179078200-179078400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr5:179078200-179085400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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