Variant report

Variant	nsv968840
Chromosome Location	chr5:90089029-90097179
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	CBX3	chr5:90092791-90093149	K562	blood:	n/a	n/a
2	CTCF	chr5:90089160-90089310	SK-N-SH_RA	brain:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
3	CTCF	chr5:90089100-90089250	AG04450	lung:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
4	CTCF	chr5:90089140-90089290	HPAF	blood vessel:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
5	CTCF	chr5:90089111-90089298	IMR90	lung:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
6	CTCF	chr5:90089060-90089210	HCT-116	colon:	n/a	chr5:90089191-90089209 chr5:90089192-90089208
7	CTCF	chr5:90089020-90089170	NB4	blood:	n/a	n/a
8	CTCF	chr5:90089040-90089190	HRE	kidney:	n/a	n/a
9	CTCF	chr5:90089155-90089209	GM12878	blood:	n/a	chr5:90089191-90089209 chr5:90089192-90089208
10	CTCF	chr5:90089160-90089310	HRPEpiC	eye:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
11	CTCF	chr5:90089100-90089250	AG09319	gingival:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
12	CTCF	chr5:90089160-90089310	HPAF	blood vessel:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
13	CTCF	chr5:90089080-90089230	AG10803	skin:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
14	CTCF	chr5:90089140-90089290	HepG2	liver:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
15	CTCF	chr5:90089100-90089250	HCPEpiC	choroid plexus:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
16	CTCF	chr5:90089106-90089268	Hela-S3	cervix:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
17	CTCF	chr5:90089140-90089290	HPF	lung:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
18	CTCF	chr5:90089120-90089270	AG04450	lung:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
19	CTCF	chr5:90089160-90089310	MCF-7	breast:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
20	CTCF	chr5:90089160-90089310	HMF	breast:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
21	CTCF	chr5:90089140-90089290	SK-N-SH_RA	brain:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
22	CTCF	chr5:90089060-90089210	AG04449	skin:	n/a	chr5:90089191-90089209 chr5:90089192-90089208
23	CTCF	chr5:90089120-90089270	HCPEpiC	choroid plexus:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
24	CTCF	chr5:90089120-90089270	GM06990	blood:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
25	CTCF	chr5:90089140-90089290	HCT-116	colon:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
26	CTCF	chr5:90089140-90089290	BJ	skin:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
27	CTCF	chr5:90089060-90089210	HRE	kidney:	n/a	chr5:90089191-90089209 chr5:90089192-90089208
28	CTCF	chr5:90089060-90089210	HCFaa	heart:	n/a	chr5:90089191-90089209 chr5:90089192-90089208
29	CTCF	chr5:90089160-90089310	AG10803	skin:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
30	CTCF	chr5:90089120-90089270	BE2_C	brain:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
31	CTCF	chr5:90089065-90089446	HCT-116	colon:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
32	CTCF	chr5:90089260-90089410	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chr5:90089131-90089317	GM12878	blood:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
34	CTCF	chr5:90089160-90089310	HA-sp	spinal cord:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
35	CTCF	chr5:90089100-90089250	HBMEC	blood vessel:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
36	CTCF	chr5:90089080-90089230	RPTEC	kidney:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
37	CTCF	chr5:90089080-90089230	GM12872	blood:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
38	CTCF	chr5:90089120-90089270	HMF	breast:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
39	CTCF	chr5:90089151-90089299	K562	blood:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
40	CTCF	chr5:90089160-90089310	BJ	skin:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
41	CTCF	chr5:90089040-90089190	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr5:90088940-90089090	GM12865	blood:	n/a	n/a
43	CTCF	chr5:90088800-90089090	HAc	cerebellar:	n/a	n/a
44	CTCF	chr5:90089120-90089270	AG04449	skin:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
45	CTCF	chr5:90089146-90089228	LNCaP	prostate:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
46	CTCF	chr5:90089120-90089270	HRPEpiC	eye:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
47	CTCF	chr5:90089100-90089250	HPF	lung:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214
48	CTCF	chr5:90089060-90089210	HA-sp	spinal cord:	n/a	chr5:90089191-90089209 chr5:90089192-90089208
49	CTCF	chr5:90088960-90089110	HCM	heart:	n/a	n/a
50	CTCF	chr5:90089140-90089290	NHEK	skin:	n/a	chr5:90089191-90089209 chr5:90089192-90089208 chr5:90089193-90089214

No.	Distal block	Cell Line	Cell type
1	chr5:90079294..90080237-chr5:90089325..90090028,2	MCF-7	breast:
2	chr5:90087371..90091009-chr5:90095949..90098739,3	K562	blood:
3	chr5:90088753..90091420-chr5:90094556..90098739,3	K562	blood:
4	chr5:90087371..90091009-chr5:90095949..90098739,3	K562	blood:
5	chr5:90096168..90100170-chr5:90100942..90103873,3	K562	blood:
6	chr5:90088753..90091420-chr5:90094556..90098739,3	K562	blood:
7	chr5:89769110..89772331-chr5:90086907..90091587,4	K562	blood:

Variant related genes	Relation type
GPR98	TF binding region
ENSG00000176055	chromatin interactions
ENSG00000113356	chromatin interactions

Extended variants
information (count: 322 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:322 , 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	rs150575580	chr5:90089116-90089117	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs116622509	chr5:90089127-90089128	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs567556126	chr5:90089128-90089129	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs138578336	chr5:90089140-90089141	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs556149471	chr5:90089173-90089174	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs374725628	chr5:90089248-90089249	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs576117584	chr5:90089296-90089297	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs17554723	chr5:90089314-90089315	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs149333603	chr5:90089316-90089317	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs374127029	chr5:90089326-90089327	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs78376165	chr5:90089357-90089358	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs147422668	chr5:90089359-90089360	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs74617980	chr5:90089375-90089376	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs80328833	chr5:90089420-90089421	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs187662714	chr5:90089421-90089422	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs16869138	chr5:90089437-90089438	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs139895324	chr5:90089443-90089444	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs34606770	chr5:90089526-90089527	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs72225806	chr5:90089527-90089528	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs141159103	chr5:90089552-90089553	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs191541124	chr5:90089563-90089564	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs16869139	chr5:90089566-90089567	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs2443070	chr5:90089612-90089613	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs16869140	chr5:90089651-90089652	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs567474081	chr5:90089669-90089670	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs374327848	chr5:90089687-90089688	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs536511102	chr5:90089723-90089724	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs143787901	chr5:90089817-90089818	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs377528204	chr5:90089832-90089833	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs77395387	chr5:90089837-90089838	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs550072050	chr5:90089842-90089843	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs532932836	chr5:90089844-90089845	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs538237208	chr5:90089856-90089857	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs558559448	chr5:90089859-90089860	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs572038562	chr5:90089893-90089894	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs541168557	chr5:90089898-90089899	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs569984858	chr5:90089945-90089946	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs78879431	chr5:90089980-90089981	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs79316782	chr5:90089981-90089982	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs549199611	chr5:90090049-90090050	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs532541680	chr5:90090092-90090093	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs563613781	chr5:90090111-90090112	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs111844265	chr5:90090112-90090113	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs371798574	chr5:90090165-90090166	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs183711789	chr5:90090184-90090185	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs559744172	chr5:90090332-90090333	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs4916821	chr5:90090399-90090400	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs534464330	chr5:90090411-90090412	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs2438361	chr5:90090437-90090438	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs577572695	chr5:90090456-90090457	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:90048400-90089200	Strong transcription	HUES48 Cell Line	embryonic stem cell
2	chr5:90051800-90105000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr5:90061200-90090800	Weak transcription	Brain Anterior Caudate	brain
4	chr5:90066200-90089800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr5:90069400-90089400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:90078400-90089800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr5:90079600-90089400	Weak transcription	Fetal Brain Male	brain
8	chr5:90082200-90089800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:90082200-90090000	Strong transcription	H1 Cell Line	embryonic stem cell
10	chr5:90082600-90090200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
11	chr5:90082800-90090600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:90083600-90089200	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr5:90083600-90090400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr5:90085200-90090400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr5:90085200-90090400	Weak transcription	Pancreas	Pancrea
16	chr5:90086200-90090200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr5:90086200-90090200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr5:90086200-90092200	Strong transcription	Cortex derived primary cultured neurospheres	brain
19	chr5:90086600-90090600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr5:90086600-90091800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr5:90086800-90089800	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr5:90086800-90090400	Strong transcription	H9 Cell Line	embryonic stem cell
23	chr5:90087000-90090200	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr5:90087000-90091800	Strong transcription	Fetal Brain Female	brain
25	chr5:90087200-90089600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr5:90087400-90090800	ZNF genes & repeats	K562	blood
27	chr5:90087600-90089600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr5:90088400-90089400	Enhancers	Fetal Heart	heart
29	chr5:90088600-90092200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
30	chr5:90089000-90090600	Weak transcription	Brain Germinal Matrix	brain
31	chr5:90089200-90091800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
32	chr5:90089200-90092400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
33	chr5:90089400-90090400	Strong transcription	Fetal Brain Male	brain
34	chr5:90089400-90092000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr5:90089600-90090600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr5:90089600-90091000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
37	chr5:90089800-90090000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
38	chr5:90089800-90091200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
39	chr5:90089800-90092400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:90089800-90092600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr5:90090000-90092200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
42	chr5:90090200-90091400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
43	chr5:90090200-90092400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr5:90090400-90090600	ZNF genes & repeats	Fetal Brain Male	brain
45	chr5:90090400-90090800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:90090400-90090800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
47	chr5:90090600-90091000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr5:90090600-90091800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr5:90090600-90092000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr5:90090600-90092000	ZNF genes & repeats	Brain Germinal Matrix	brain

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