Variant report

Variant	esv3341464
Chromosome Location	chr18:12428452-12432250
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:42)
CpG islands
(count:305)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:42 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr18:12430406-12431190	GM12878	blood:	n/a	n/a
2	BCL3	chr18:12430339-12431103	GM12878	blood:	n/a	n/a
3	CTCF	chr18:12430708-12431101	GM19239	blood:	n/a	n/a
4	CTCF	chr18:12429880-12430030	Hela-S3	cervix:	n/a	chr18:12430002-12430011
5	CTCF	chr18:12430294-12430621	GM19239	blood:	n/a	n/a
6	CTCF	chr18:12429960-12430110	HEK293	kidney:	n/a	chr18:12430002-12430011 chr18:12430037-12430046
7	EGR1	chr18:12431367-12431702	K562	blood:	n/a	n/a
8	MAFK	chr18:12430663-12430737	K562	blood:	n/a	n/a
9	MAX	chr18:12430667-12431042	NB4	blood:	n/a	chr18:12430903-12430913
10	MYC	chr18:12430738-12430876	MCF-7	breast:	n/a	n/a
11	MYC	chr18:12430377-12430387	MCF-7	breast:	n/a	n/a
12	MYC	chr18:12430597-12430793	HUVEC	blood vessel:	n/a	n/a
13	MYC	chr18:12430554-12430652	GM12878	blood:	n/a	n/a
14	MYC	chr18:12430824-12431105	HUVEC	blood vessel:	n/a	chr18:12430903-12430913
15	NFATC1	chr18:12430240-12431249	GM12878	blood:	n/a	n/a
16	NFATC1	chr18:12430449-12431222	GM12878	blood:	n/a	n/a
17	NR2C2	chr18:12430262-12431063	GM12878	blood:	n/a	n/a
18	PBX3	chr18:12430904-12431089	GM12878	blood:	n/a	n/a
19	POLR2A	chr18:12430657-12430937	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr18:12430490-12430637	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr18:12430320-12430349	A549	lung:	n/a	n/a
22	POLR2A	chr18:12428825-12429165	HepG2	liver:	n/a	n/a
23	POLR2A	chr18:12427775-12428456	HepG2	liver:	n/a	n/a
24	POLR2A	chr18:12429476-12429495	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr18:12430802-12430805	ProgFib	skin:	n/a	n/a
26	POLR2A	chr18:12430377-12431206	HepG2	liver:	n/a	n/a
27	POLR2A	chr18:12430324-12430622	K562	blood:	n/a	n/a
28	POLR2A	chr18:12430778-12430811	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr18:12430838-12430856	ProgFib	skin:	n/a	n/a
30	POLR2A	chr18:12430445-12431005	HepG2	liver:	n/a	n/a
31	POLR2A	chr18:12430028-12431318	HepG2	liver:	n/a	n/a
32	POLR2A	chr18:12430408-12430878	HepG2	liver:	n/a	n/a
33	POLR2A	chr18:12430061-12431062	GM12892	blood:	n/a	n/a
34	POLR2A	chr18:12429499-12429572	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr18:12429059-12429068	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr18:12430252-12430655	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr18:12430352-12430375	A549	lung:	n/a	n/a
38	STAT5A	chr18:12430338-12431073	GM12878	blood:	n/a	n/a
39	STAT5A	chr18:12430271-12431134	GM12878	blood:	n/a	n/a
40	STAT5A	chr18:12430552-12431104	K562	blood:	n/a	n/a
41	SUZ12	chr18:12430293-12431131	H1-hESC	embryonic stem cell:	n/a	n/a
42	TBL1XR1	chr18:12430808-12430909	K562	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:12431241-12431291	U87	brain:	n/a
2	chr18:12431464-12431514	NHBE	bronchial:	n/a
3	chr18:12431464-12431514	IMR90	lung:	fetal
4	chr18:12431554-12431604	NT2-D1	testis:	n/a
5	chr18:12429989-12430039	HRCEpiC	kidney:	n/a
6	chr18:12431554-12431604	NH-A	brain:	n/a
7	chr18:12431241-12431291	NB4	blood:	n/a
8	chr18:12431554-12431604	SKMC	muscle:	n/a
9	chr18:12431464-12431514	HEEpiC	esophagus:	n/a
10	chr18:12431554-12431604	HMEC	breast:	n/a
11	chr18:12431241-12431291	HRPEpiC	eye:	n/a
12	chr18:12429989-12430039	AG04449	skin:	fetal
13	chr18:12431464-12431514	AG09309	skin:	n/a
14	chr18:12431241-12431291	A549	lung:	n/a
15	chr18:12429989-12430039	NHBE	bronchial:	n/a
16	chr18:12429989-12430039	HCM	heart:	n/a
17	chr18:12431241-12431291	HRE	kidney:	n/a
18	chr18:12429120-12429170	HEK293	kidney:	embryo
19	chr18:12431241-12431291	HMEC	breast:	n/a
20	chr18:12431554-12431604	AG04449	skin:	fetal
21	chr18:12431241-12431291	HEK293	kidney:	embryo
22	chr18:12431241-12431291	BJ	skin:	n/a
23	chr18:12429989-12430039	RPTEC	kidney:	n/a
24	chr18:12429120-12429170	GM12878	blood:	n/a
25	chr18:12431554-12431604	ProgFib	skin:	n/a
26	chr18:12429120-12429170	LNCaP	prostate:	n/a
27	chr18:12431464-12431514	NB4	blood:	n/a
28	chr18:12431241-12431291	GM12891	blood:	n/a
29	chr18:12431464-12431514	HRCEpiC	kidney:	n/a
30	chr18:12429989-12430039	Jurkat	blood:	n/a
31	chr18:12431241-12431291	HepG2	liver:	n/a
32	chr18:12431554-12431604	IMR90	lung:	fetal
33	chr18:12431554-12431604	RPTEC	kidney:	n/a
34	chr18:12429989-12430039	ECC-1	luminal epithelium:	n/a
35	chr18:12431464-12431514	Hepatocyte	liver:	n/a
36	chr18:12431241-12431291	AG09309	skin:	n/a
37	chr18:12431554-12431604	PrEC	prostate:	n/a
38	chr18:12429120-12429170	GM06990	blood:	n/a
39	chr18:12431464-12431514	BJ	skin:	n/a
40	chr18:12431241-12431291	NHDF-neo	bronchial:	n/a
41	chr18:12429989-12430039	AG04450	lung:	fetal
42	chr18:12431241-12431291	HPAEpiC	pulmonary alveolar:	n/a
43	chr18:12431241-12431291	HL-60	blood:	n/a
44	chr18:12429120-12429170	Hela-S3	cervix:	n/a
45	chr18:12429989-12430039	SAEC	small airway:	n/a
46	chr18:12431554-12431604	NB4	blood:	n/a
47	chr18:12431554-12431604	MCF10A-Er-Src	breast:	n/a
48	chr18:12431464-12431514	PrEC	prostate:	n/a
49	chr18:12429120-12429170	NHDF-neo	bronchial:	n/a
50	chr18:12429120-12429170	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr18:12428003..12430631-chr18:12490469..12492690,2	K562	blood:
2	chr18:12427958..12434396-chr18:12436312..12440619,6	K562	blood:
3	chr18:12427173..12429276-chr18:12453042..12455618,2	K562	blood:
4	chr18:12422115..12425082-chr18:12427051..12428777,2	K562	blood:
5	chr18:12418687..12420720-chr18:12430201..12431737,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TUBB6-2	chr18:12431581-12432232	NONHSAT058369

No data

Variant related genes	Relation type
ENSG00000256786	TF binding region
ENSG00000267108	TF binding region
ENSG00000256786	CpG island
ENSG00000267108	CpG island
ENSG00000141391	chromatin interactions
ENSG00000267199	chromatin interactions
ENSG00000134278	chromatin interactions

Extended variants
information (count: 188 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:188 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530262370	chr18:12428460-12428461	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs535018200	chr18:12428464-12428465	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs149731199	chr18:12428553-12428554	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs548750210	chr18:12428554-12428555	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs147821539	chr18:12428594-12428595	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs529538	chr18:12428617-12428618	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs183360580	chr18:12428624-12428625	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs76431133	chr18:12428640-12428641	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs141656460	chr18:12428684-12428685	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs188765258	chr18:12428710-12428711	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs540181612	chr18:12428737-12428738	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs114735380	chr18:12428745-12428746	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs539821668	chr18:12428762-12428763	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs546623608	chr18:12428776-12428777	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs145397828	chr18:12428809-12428810	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs538619134	chr18:12428867-12428868	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs560518021	chr18:12428875-12428876	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs373379461	chr18:12428951-12428952	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs544399600	chr18:12428981-12428982	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs562341074	chr18:12428985-12428986	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs376395216	chr18:12429001-12429002	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs530951654	chr18:12429039-12429040	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs552237212	chr18:12429052-12429053	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs116649616	chr18:12429053-12429054	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs3760548	chr18:12429071-12429072	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs546642584	chr18:12429121-12429122	Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs3760549	chr18:12429202-12429203	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs535726141	chr18:12429230-12429231	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs557576638	chr18:12429232-12429233	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs569461852	chr18:12429239-12429240	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs147672462	chr18:12429251-12429252	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs557912121	chr18:12429261-12429262	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs572943673	chr18:12429280-12429281	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs3760550	chr18:12429313-12429314	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs371888566	chr18:12429337-12429338	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs147870479	chr18:12429351-12429352	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs141682055	chr18:12429361-12429362	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs143717130	chr18:12429363-12429364	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs375241002	chr18:12429371-12429372	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs151054907	chr18:12429381-12429382	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs562376554	chr18:12429391-12429392	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs368285489	chr18:12429444-12429445	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs111448892	chr18:12429450-12429451	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532939130	chr18:12429503-12429504	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs544775178	chr18:12429515-12429516	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs142323080	chr18:12429526-12429527	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs371016378	chr18:12429552-12429553	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs192945958	chr18:12429571-12429572	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs546973512	chr18:12429594-12429595	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs374439530	chr18:12429600-12429601	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:193 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12410400-12430400	Weak transcription	A549	lung
2	chr18:12418200-12430400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr18:12420200-12434800	Weak transcription	Stomach Mucosa	stomach
4	chr18:12420600-12430000	Weak transcription	Pancreas	Pancrea
5	chr18:12420600-12432400	Weak transcription	Left Ventricle	heart
6	chr18:12420600-12432600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr18:12420600-12433600	Weak transcription	Duodenum Mucosa	Duodenum
8	chr18:12420600-12443600	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr18:12420600-12477600	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr18:12421200-12429600	Weak transcription	Gastric	stomach
11	chr18:12421200-12429600	Weak transcription	Spleen	Spleen
12	chr18:12421200-12432400	Weak transcription	Esophagus	oesophagus
13	chr18:12421200-12443400	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr18:12421200-12447600	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr18:12421200-12452800	Weak transcription	Colonic Mucosa	Colon
16	chr18:12421400-12430800	Weak transcription	Adipose Nuclei	Adipose
17	chr18:12421400-12431200	Weak transcription	Right Ventricle	heart
18	chr18:12421400-12433600	Weak transcription	Placenta	Placenta
19	chr18:12421400-12434600	Weak transcription	Colon Smooth Muscle	Colon
20	chr18:12421400-12444200	Weak transcription	Rectal Smooth Muscle	rectum
21	chr18:12421800-12428800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr18:12421800-12430400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr18:12421800-12434400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr18:12421800-12442400	Weak transcription	GM12878-XiMat	blood
25	chr18:12422000-12431800	Weak transcription	Fetal Thymus	thymus
26	chr18:12422600-12430400	Weak transcription	K562	blood
27	chr18:12424000-12430000	Weak transcription	Thymus	Thymus
28	chr18:12426600-12428600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr18:12426600-12428800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
30	chr18:12426600-12428800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr18:12426600-12428800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr18:12426600-12428800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr18:12426600-12429000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr18:12426600-12430000	Strong transcription	Ovary	ovary
35	chr18:12426600-12433200	Strong transcription	Brain Angular Gyrus	brain
36	chr18:12426600-12434200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr18:12426600-12434600	Strong transcription	Brain Germinal Matrix	brain
38	chr18:12426600-12434600	Strong transcription	NHLF	lung
39	chr18:12426600-12434800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr18:12426600-12435000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr18:12426600-12435400	Strong transcription	Fetal Muscle Trunk	muscle
42	chr18:12426600-12438600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr18:12426800-12428600	ZNF genes & repeats	NH-A	brain
44	chr18:12426800-12429200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr18:12426800-12430200	Strong transcription	Duodenum Smooth Muscle	Duodenum
46	chr18:12426800-12431200	Strong transcription	Osteobl	bone
47	chr18:12426800-12431800	Strong transcription	Stomach Smooth Muscle	stomach
48	chr18:12426800-12433400	Strong transcription	HepG2	liver
49	chr18:12426800-12434400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr18:12426800-12436400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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