Variant report

Variant	nsv599481
Chromosome Location	chr5:115540041-115609552
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:303)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:115567073-115567351	HepG2	liver:	n/a	n/a
2	BACH1	chr5:115573174-115573254	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr5:115609206-115609493	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
4	BATF	chr5:115609200-115609492	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
5	CEBPB	chr5:115608269-115608767	MCF-7	breast:	n/a	chr5:115608483-115608494
6	CEBPB	chr5:115601292-115601498	HepG2	liver:	n/a	n/a
7	CEBPB	chr5:115608227-115608718	MCF-7	breast:	n/a	chr5:115608483-115608494
8	CEBPB	chr5:115608311-115608872	IMR90	lung:	n/a	chr5:115608483-115608494
9	CEBPB	chr5:115584254-115584389	K562	blood:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
10	CEBPB	chr5:115584135-115584482	HepG2	liver:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
11	CEBPB	chr5:115584119-115584488	MCF-7	breast:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
12	CEBPB	chr5:115584226-115584373	HepG2	liver:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
13	CEBPB	chr5:115608381-115608622	HepG2	liver:	n/a	chr5:115608483-115608494
14	CEBPB	chr5:115608357-115608659	A549	lung:	n/a	chr5:115608483-115608494
15	CHD2	chr5:115609186-115609453	GM12878	blood:	n/a	n/a
16	CHD2	chr5:115608466-115608624	GM12878	blood:	n/a	n/a
17	CTCF	chr5:115573720-115573870	HepG2	liver:	n/a	n/a
18	CTCF	chr5:115573640-115573790	A549	lung:	n/a	n/a
19	CTCF	chr5:115573720-115573950	WI-38	lung:	n/a	n/a
20	CTCF	chr5:115573720-115573870	HA-sp	spinal cord:	n/a	n/a
21	CTCF	chr5:115608440-115608590	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:115573720-115573870	AG10803	skin:	n/a	n/a
23	CTCF	chr5:115605340-115605490	AG10803	skin:	n/a	n/a
24	CTCF	chr5:115573740-115573890	HEK293	kidney:	n/a	n/a
25	CTCF	chr5:115573752-115573865	K562	blood:	n/a	n/a
26	CTCF	chr5:115573700-115573850	GM12872	blood:	n/a	n/a
27	CTCF	chr5:115608409-115608558	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr5:115573669-115573951	K562	blood:	n/a	n/a
29	CTCF	chr5:115608440-115608590	A549	lung:	n/a	n/a
30	CTCF	chr5:115573700-115573850	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr5:115573700-115573850	HEK293	kidney:	n/a	n/a
32	CTCF	chr5:115608340-115608490	BE2_C	brain:	n/a	n/a
33	CTCF	chr5:115573700-115573850	GM12875	blood:	n/a	n/a
34	CTCF	chr5:115608000-115608150	GM12872	blood:	n/a	n/a
35	CTCF	chr5:115573740-115573890	HCT-116	colon:	n/a	n/a
36	CTCF	chr5:115573680-115573830	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr5:115573740-115573890	AG10803	skin:	n/a	n/a
38	CTCF	chr5:115573740-115573890	GM12878	blood:	n/a	n/a
39	CTCF	chr5:115608440-115608590	GM12869	blood:	n/a	n/a
40	CTCF	chr5:115573760-115573910	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr5:115573695-115573940	IMR90	lung:	n/a	n/a
42	CTCF	chr5:115608380-115608530	GM12868	blood:	n/a	n/a
43	CTCF	chr5:115608200-115608470	GM12873	blood:	n/a	n/a
44	CTCF	chr5:115573738-115573823	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr5:115608400-115608550	GM06990	blood:	n/a	n/a
46	CTCF	chr5:115608400-115608550	NHLF	lung:	n/a	n/a
47	CTCF	chr5:115573760-115573910	MCF-7	breast:	n/a	n/a
48	CTCF	chr5:115573820-115573970	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr5:115608380-115608530	GM12873	blood:	n/a	n/a
50	CTCF	chr5:115573680-115573830	GM12864	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:115599680-115599730	HCF	heart:	n/a
2	chr5:115599680-115599730	U87	brain:	n/a
3	chr5:115599680-115599730	Caco-2	colon:	n/a
4	chr5:115599680-115599730	NH-A	brain:	n/a
5	chr5:115599680-115599730	HepG2	liver:	n/a
6	chr5:115599680-115599730	HIPEpiC	eye:	n/a
7	chr5:115599680-115599730	AG09319	gingival:	n/a
8	chr5:115599680-115599730	HCT-116	colon:	n/a
9	chr5:115599680-115599730	ProgFib	skin:	n/a
10	chr5:115599680-115599730	PANC-1	pancreas:	n/a
11	chr5:115599680-115599730	BE2_C	brain:	n/a
12	chr5:115599680-115599730	Hepatocyte	liver:	n/a
13	chr5:115599680-115599730	T-47D	breast:	n/a
14	chr5:115599680-115599730	HRCEpiC	kidney:	n/a
15	chr5:115599680-115599730	AG04449	skin:	fetal
16	chr5:115599680-115599730	ovcar-3	ovarian:	n/a
17	chr5:115599680-115599730	GM12878	blood:	n/a
18	chr5:115599680-115599730	GM19239	blood:	n/a
19	chr5:115599680-115599730	HCM	heart:	n/a
20	chr5:115599680-115599730	HEEpiC	esophagus:	n/a
21	chr5:115599680-115599730	GM06990	blood:	n/a
22	chr5:115599680-115599730	A549	lung:	n/a
23	chr5:115599680-115599730	AG04450	lung:	fetal
24	chr5:115599680-115599730	NHDF-neo	bronchial:	n/a
25	chr5:115599680-115599730	AG10803	skin:	n/a
26	chr5:115599680-115599730	K562	blood:	n/a
27	chr5:115599680-115599730	HL-60	blood:	n/a
28	chr5:115599680-115599730	HNPCEpiC	eye:	n/a
29	chr5:115599680-115599730	RPTEC	kidney:	n/a
30	chr5:115599680-115599730	H1-hESC	embryonic stem cell:	embryo
31	chr5:115599680-115599730	CMK	blood:	n/a
32	chr5:115599680-115599730	SK-N-SH	brain:	n/a
33	chr5:115599680-115599730	SK-N-SH_RA	brain:	n/a
34	chr5:115599680-115599730	PFSK-1	brain:	n/a
35	chr5:115599680-115599730	NB4	blood:	n/a
36	chr5:115599680-115599730	HAEpiC	amniotic membrane:	n/a
37	chr5:115599680-115599730	HRPEpiC	eye:	n/a
38	chr5:115599680-115599730	HUVEC	blood vessel:	n/a
39	chr5:115599680-115599730	SK-N-MC	brain:	n/a
40	chr5:115599680-115599730	HPAEpiC	pulmonary alveolar:	n/a
41	chr5:115599680-115599730	Jurkat	blood:	n/a
42	chr5:115599680-115599730	HEK293	kidney:	embryo
43	chr5:115599680-115599730	MCF-7	breast:	n/a
44	chr5:115599680-115599730	HRE	kidney:	n/a
45	chr5:115599680-115599730	BJ	skin:	n/a
46	chr5:115599680-115599730	LNCaP	prostate:	n/a
47	chr5:115599680-115599730	HCPEpiC	choroid plexus:	n/a
48	chr5:115599680-115599730	Hela-S3	cervix:	n/a
49	chr5:115599680-115599730	NT2-D1	testis:	n/a
50	chr5:115599680-115599730	SKMC	muscle:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:115573428..115574084-chr5:115607901..115608709,2	MCF-7	breast:
2	chr5:115523919..115526832-chr5:115553749..115555427,2	MCF-7	breast:
3	chr5:115473639..115474170-chr5:115607611..115608509,2	MCF-7	breast:
4	chr5:115573428..115574084-chr5:115607901..115608709,2	MCF-7	breast:
5	chr5:115607181..115609929-chr5:115613382..115615949,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEMA6A-7	chr5:115553723-115553992	NONHSAT103356
2	lnc-LVRN.1-3	chr5:115549572-115550152	NONHSAT103355

No data

Variant related genes	Relation type
HMGN2P27	TF binding region
HMGN2P27	CpG island
ENSG00000212457	chromatin interactions

Extended variants
information (count: 3602 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3602 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11241377	chr5:115540041-115540042	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571797525	chr5:115540057-115540058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542253586	chr5:115540078-115540079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs150329502	chr5:115540127-115540128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371205347	chr5:115540130-115540131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561274239	chr5:115540174-115540175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552804978	chr5:115540185-115540186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566528975	chr5:115540186-115540187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79836123	chr5:115540189-115540190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs62384237	chr5:115540222-115540223	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs574878756	chr5:115540224-115540225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370767321	chr5:115540237-115540238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188909542	chr5:115540257-115540258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs193100287	chr5:115540280-115540281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7709426	chr5:115540310-115540311	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs577770889	chr5:115540341-115540342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550320049	chr5:115540343-115540344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs137882851	chr5:115540383-115540384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564755767	chr5:115540399-115540400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532160537	chr5:115540500-115540501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12658625	chr5:115540523-115540524	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs367981358	chr5:115540529-115540530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369845078	chr5:115540540-115540541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs77285160	chr5:115540569-115540570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7709377	chr5:115540573-115540574	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
26	rs112156775	chr5:115540586-115540587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527726948	chr5:115540605-115540606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149042405	chr5:115540616-115540617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143181169	chr5:115540624-115540625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527898985	chr5:115540637-115540638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547943203	chr5:115540645-115540646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185567428	chr5:115540654-115540655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs138978216	chr5:115540664-115540665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567603288	chr5:115540689-115540690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142895268	chr5:115540702-115540703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537406093	chr5:115540750-115540751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566194643	chr5:115540759-115540760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147394089	chr5:115540760-115540761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577840617	chr5:115540762-115540763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1541654	chr5:115540836-115540837	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs138129557	chr5:115540843-115540844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573744435	chr5:115540851-115540852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556781078	chr5:115540863-115540864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554108371	chr5:115540935-115540936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143077621	chr5:115541002-115541003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562926499	chr5:115541063-115541064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376491185	chr5:115541074-115541075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs72804883	chr5:115541102-115541103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545390075	chr5:115541117-115541118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139244449	chr5:115541128-115541129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
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
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	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
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115518800-115548000	Weak transcription	Psoas Muscle	Psoas
2	chr5:115522600-115540200	Weak transcription	Primary B cells from peripheral blood	blood
3	chr5:115525800-115560000	Weak transcription	Left Ventricle	heart
4	chr5:115527800-115543800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:115537200-115559400	Weak transcription	Primary B cells from cord blood	blood
6	chr5:115537400-115545000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr5:115537400-115560000	Weak transcription	Primary T cells from cord blood	blood
8	chr5:115537600-115542400	Weak transcription	Fetal Intestine Large	intestine
9	chr5:115537600-115560200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr5:115542600-115562800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr5:115543200-115543800	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr5:115543800-115545800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr5:115544000-115544400	Enhancers	Ovary	ovary
14	chr5:115545800-115549600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr5:115547400-115548000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr5:115547400-115548200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr5:115548000-115548200	Enhancers	Psoas Muscle	Psoas
18	chr5:115549600-115550400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr5:115549800-115560000	Weak transcription	Fetal Intestine Small	intestine
20	chr5:115550400-115556400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr5:115551800-115576400	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr5:115553400-115560200	Weak transcription	Fetal Stomach	stomach
23	chr5:115555000-115555800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:115555000-115557200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr5:115555800-115556400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr5:115556400-115556600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:115556800-115557000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr5:115557000-115562800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:115557200-115557400	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr5:115557400-115560200	Weak transcription	Pancreas	Pancrea
31	chr5:115557400-115580800	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr5:115557400-115583200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr5:115557600-115561000	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr5:115559200-115564000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr5:115559200-115578400	Weak transcription	Fetal Lung	lung
36	chr5:115559400-115560000	ZNF genes & repeats	Primary B cells from cord blood	blood
37	chr5:115559800-115560000	Active TSS	Liver	Liver
38	chr5:115559800-115561400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr5:115560000-115560200	Strong transcription	Left Ventricle	heart
40	chr5:115560000-115560400	Strong transcription	Primary B cells from cord blood	blood
41	chr5:115560000-115560400	ZNF genes & repeats	Primary T cells from cord blood	blood
42	chr5:115560000-115560400	ZNF genes & repeats	Fetal Intestine Small	intestine
43	chr5:115560000-115560600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
44	chr5:115560000-115561800	Weak transcription	Liver	Liver
45	chr5:115560000-115563400	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr5:115560000-115563600	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr5:115560200-115560400	ZNF genes & repeats	Fetal Stomach	stomach
48	chr5:115560200-115560400	ZNF genes & repeats	Left Ventricle	heart
49	chr5:115560200-115560400	ZNF genes & repeats	Pancreas	Pancrea
50	chr5:115560200-115560600	ZNF genes & repeats	Primary hematopoietic stem cells	blood

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