Variant report

Variant	esv3356263
Chromosome Location	chr18:9614152-9615550
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:468)
CpG islands
(count:305)
Chromatin interactive
region (count:24)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:468 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:9615316-9615343	K562	blood:	n/a	n/a
2	BACH1	chr18:9614924-9615365	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr18:9613850-9614215	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr18:9613533-9614307	GM12878	blood:	n/a	chr18:9613942-9613955
5	BCLAF1	chr18:9614980-9615345	GM12878	blood:	n/a	n/a
6	BHLHE40	chr18:9615193-9615231	GM12878	blood:	n/a	n/a
7	BHLHE40	chr18:9614571-9614942	GM12878	blood:	n/a	chr18:9614847-9614863 chr18:9614823-9614839
8	BHLHE40	chr18:9615211-9615252	K562	blood:	n/a	n/a
9	BRCA1	chr18:9613818-9614166	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr18:9615220-9615258	HepG2	liver:	n/a	n/a
11	CBX3	chr18:9615013-9615553	K562	blood:	n/a	n/a
12	CCNT2	chr18:9613769-9615322	K562	blood:	n/a	chr18:9615058-9615067 chr18:9615031-9615040
13	CEBPB	chr18:9614962-9614975	HepG2	liver:	n/a	n/a
14	CEBPB	chr18:9614898-9615080	Hela-S3	cervix:	n/a	n/a
15	CEBPD	chr18:9614302-9615025	HepG2	liver:	n/a	n/a
16	CHD1	chr18:9614808-9615019	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr18:9613825-9614260	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr18:9613863-9614191	K562	blood:	n/a	n/a
19	CHD2	chr18:9613874-9614211	GM12878	blood:	n/a	n/a
20	CHD2	chr18:9614524-9615426	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr18:9613860-9614298	HepG2	liver:	n/a	n/a
22	CHD2	chr18:9614528-9614562	HepG2	liver:	n/a	n/a
23	CHD2	chr18:9615158-9615326	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr18:9613665-9614293	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr18:9614986-9615168	GM12878	blood:	n/a	n/a
26	CREB1	chr18:9613816-9614222	A549	lung:	n/a	n/a
27	CREB1	chr18:9614691-9615008	A549	lung:	n/a	n/a
28	CTCF	chr18:9615200-9615350	AG10803	skin:	n/a	chr18:9615277-9615286 chr18:9615277-9615290
29	CTCF	chr18:9613977-9614204	GM12892	blood:	n/a	chr18:9614097-9614110
30	CTCF	chr18:9614219-9614263	Fibrobl	skin:	n/a	n/a
31	CTCF	chr18:9614140-9614290	NHEK	skin:	n/a	n/a
32	CTCF	chr18:9614140-9614290	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr18:9613979-9614176	HepG2	liver:	n/a	chr18:9614097-9614110
34	CTCF	chr18:9613995-9614173	GM12891	blood:	n/a	chr18:9614097-9614110
35	CTCF	chr18:9613919-9614233	GM12878	blood:	n/a	chr18:9614097-9614110
36	CTCF	chr18:9614028-9614172	GM19238	blood:	n/a	chr18:9614097-9614110
37	CTCF	chr18:9614043-9614164	NHEK	skin:	n/a	chr18:9614097-9614110
38	CTCF	chr18:9614020-9614170	GM12867	blood:	n/a	chr18:9614097-9614110
39	CTCF	chr18:9614160-9614310	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr18:9614020-9614170	AG09319	gingival:	n/a	chr18:9614097-9614110
41	CTCF	chr18:9613847-9614354	K562	blood:	n/a	chr18:9614097-9614110
42	CTCF	chr18:9614080-9614230	AG04450	lung:	n/a	chr18:9614097-9614110
43	CTCF	chr18:9614020-9614170	SK-N-SH_RA	brain:	n/a	chr18:9614097-9614110
44	CTCF	chr18:9614008-9614170	GM10266	blood:	n/a	chr18:9614097-9614110
45	CTCF	chr18:9613984-9614278	K562	blood:	n/a	chr18:9614097-9614110
46	CTCF	chr18:9615279-9615293	GM12878	blood:	n/a	n/a
47	CTCF	chr18:9614564-9614580	GM12878	blood:	n/a	n/a
48	CTCF	chr18:9614160-9614310	Hela-S3	cervix:	n/a	n/a
49	CTCFL	chr18:9613877-9614240	K562	blood:	n/a	n/a
50	CTCFL	chr18:9613947-9614157	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	chr18:9614450-9614500	NB4	blood:	n/a
2	chr18:9614206-9614256	HMEC	breast:	n/a
3	chr18:9614450-9614500	CMK	blood:	n/a
4	chr18:9615155-9615205	ovcar-3	ovarian:	n/a
5	chr18:9615155-9615205	HCPEpiC	choroid plexus:	n/a
6	chr18:9615209-9615259	HRPEpiC	eye:	n/a
7	chr18:9615209-9615259	HRCEpiC	kidney:	n/a
8	chr18:9615155-9615205	BE2_C	brain:	n/a
9	chr18:9615209-9615259	HCF	heart:	n/a
10	chr18:9615093-9615143	Hepatocyte	liver:	n/a
11	chr18:9614450-9614500	HAEpiC	amniotic membrane:	n/a
12	chr18:9615209-9615259	HL-60	blood:	n/a
13	chr18:9615155-9615205	NHBE	bronchial:	n/a
14	chr18:9614450-9614500	HNPCEpiC	eye:	n/a
15	chr18:9615209-9615259	A549	lung:	n/a
16	chr18:9614206-9614256	AG04450	lung:	fetal
17	chr18:9615155-9615205	Jurkat	blood:	n/a
18	chr18:9614206-9614256	MCF10A-Er-Src	breast:	n/a
19	chr18:9615155-9615205	HCM	heart:	n/a
20	chr18:9614206-9614256	Hela-S3	cervix:	n/a
21	chr18:9614206-9614256	HEEpiC	esophagus:	n/a
22	chr18:9615093-9615143	AoSMC	blood vessel:	n/a
23	chr18:9614206-9614256	Jurkat	blood:	n/a
24	chr18:9614206-9614256	HCF	heart:	n/a
25	chr18:9615209-9615259	Jurkat	blood:	n/a
26	chr18:9615093-9615143	AG04449	skin:	fetal
27	chr18:9615155-9615205	HRE	kidney:	n/a
28	chr18:9615093-9615143	HRPEpiC	eye:	n/a
29	chr18:9615209-9615259	HUVEC	blood vessel:	n/a
30	chr18:9615155-9615205	Caco-2	colon:	n/a
31	chr18:9615155-9615205	NHDF-neo	bronchial:	n/a
32	chr18:9615209-9615259	HCM	heart:	n/a
33	chr18:9615155-9615205	ProgFib	skin:	n/a
34	chr18:9615155-9615205	AG04449	skin:	fetal
35	chr18:9615093-9615143	PrEC	prostate:	n/a
36	chr18:9614450-9614500	HRE	kidney:	n/a
37	chr18:9614450-9614500	HCPEpiC	choroid plexus:	n/a
38	chr18:9615155-9615205	HPAEpiC	pulmonary alveolar:	n/a
39	chr18:9615093-9615143	MCF10A-Er-Src	breast:	n/a
40	chr18:9615093-9615143	NHBE	bronchial:	n/a
41	chr18:9615209-9615259	NB4	blood:	n/a
42	chr18:9614450-9614500	HEEpiC	esophagus:	n/a
43	chr18:9614450-9614500	AG04449	skin:	fetal
44	chr18:9614206-9614256	A549	lung:	n/a
45	chr18:9615093-9615143	HepG2	liver:	n/a
46	chr18:9614450-9614500	PFSK-1	brain:	n/a
47	chr18:9615209-9615259	GM12892	blood:	n/a
48	chr18:9614206-9614256	HIPEpiC	eye:	n/a
49	chr18:9615093-9615143	HMEC	breast:	n/a
50	chr18:9615209-9615259	ProgFib	skin:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:9474922..9476536-chr18:9613527..9616238,2	MCF-7	breast:
2	chr18:9615456..9617526-chr18:9895448..9898198,2	K562	blood:
3	chr15:66994774..66995660-chr18:9613961..9614955,2	Hela-S3	cervix:
4	chr18:9613045..9616469-chr18:9913547..9915707,4	K562	blood:
5	chr18:9613570..9616156-chr18:9878427..9881071,2	K562	blood:
6	chr18:9614430..9615143-chr19:1249294..1250146,2	Hela-S3	cervix:
7	chr18:9613618..9614587-chr22:31686737..31687476,2	Hela-S3	cervix:
8	chr18:9569658..9574401-chr18:9612462..9616455,5	K562	blood:
9	chr18:9612544..9617098-chr18:9708301..9712595,6	MCF-7	breast:
10	chr18:9596087..9600746-chr18:9613522..9617540,6	MCF-7	breast:
11	chr18:9615287..9617165-chr18:9631128..9633561,2	K562	blood:
12	chr1:28974882..28975858-chr18:9614139..9614753,2	Hela-S3	cervix:
13	chr18:9612136..9615353-chr18:9912435..9915971,5	MCF-7	breast:
14	chr18:9593651..9596050-chr18:9613258..9616024,2	MCF-7	breast:
15	chr18:9612893..9615735-chr18:9913834..9918265,4	K562	blood:
16	chr18:9613016..9616228-chr18:9911513..9913644,4	K562	blood:
17	chr18:9584254..9588034-chr18:9613364..9615601,3	MCF-7	breast:
18	chr18:9614624..9617257-chr18:9707449..9709089,2	K562	blood:
19	chr18:9611182..9615699-chr18:9705314..9711194,13	MCF-7	breast:
20	chr17:57970172..57971882-chr18:9614484..9616129,2	MCF-7	breast:
21	chr18:9614449..9616140-chr18:9677968..9679576,2	K562	blood:
22	chr18:9594858..9597558-chr18:9614248..9616397,2	MCF-7	breast:
23	chr18:9614922..9615897-chrX:48815132..48816087,2	Hela-S3	cervix:
24	chr18:9614482..9616420-chr18:9617986..9621274,5	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RALBP1-2	chr18:9614694-9615333	NONHSAT057230
2	lnc-RALBP1-2	chr18:9615262-9615333	ENSG00000263627.1
3	lnc-PIEZO2-14	chr18:9614224-9614272	NONHSAT057228
4	lnc-RALBP1-2	chr18:9615186-9616194	NONHSAT057231

No data

Variant related genes	Relation type
ENSG00000263627	TF binding region
PPP4R1	TF binding region
ENSG00000263627	CpG island
PPP4R1	CpG island
ENSG00000068308	chromatin interactions
ENSG00000264644	chromatin interactions
ENSG00000272799	chromatin interactions
ENSG00000154845	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000212572	chromatin interactions
ENSG00000100100	chromatin interactions
ENSG00000137834	chromatin interactions
ENSG00000168461	chromatin interactions
ENSG00000101558	chromatin interactions
ENSG00000265564	chromatin interactions
ENSG00000266541	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000167470	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000108423	chromatin interactions

Extended variants
information (count: 26 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373387694	chr18:9614200-9614201	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs377081511	chr18:9614206-9614207	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs368991458	chr18:9614298-9614299	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs28461902	chr18:9614332-9614333	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
5	rs532576735	chr18:9614333-9614334	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs199537124	chr18:9614594-9614595	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
7	rs545123424	chr18:9614707-9614708	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
8	rs77036092	chr18:9614730-9614731	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
9	rs143264046	chr18:9614885-9614886	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
10	rs527335206	chr18:9614887-9614888	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
11	rs184540458	chr18:9614970-9614971	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
12	rs566883915	chr18:9614982-9614983	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
13	rs531515644	chr18:9615034-9615035	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
14	rs549776851	chr18:9615105-9615106	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
15	rs62088910	chr18:9615145-9615146	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs538437872	chr18:9615163-9615164	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
17	rs554282552	chr18:9615169-9615170	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
18	rs576648325	chr18:9615181-9615182	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
19	rs566175065	chr18:9615215-9615216	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
20	rs536696744	chr18:9615243-9615244	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
21	rs555011764	chr18:9615249-9615250	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
22	rs118132050	chr18:9615303-9615304	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
23	rs554822906	chr18:9615308-9615309	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
24	rs565493673	chr18:9615386-9615387	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
25	rs544157534	chr18:9615462-9615463	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
26	rs188897682	chr18:9615508-9615509	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Melanoma	18172304	CNVD
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
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
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	18438408	CNVD

Chromatin state (count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9612000-9615000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr18:9612200-9615200	Active TSS	NHLF	lung
3	chr18:9612400-9614800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr18:9612400-9615200	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr18:9612400-9615200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr18:9612400-9615200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr18:9612400-9615400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr18:9612400-9615800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr18:9612600-9615200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr18:9612600-9615200	Active TSS	HMEC	breast
11	chr18:9612600-9615400	Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr18:9612600-9615400	Active TSS	Ovary	ovary
13	chr18:9612600-9615600	Active TSS	Right Ventricle	heart
14	chr18:9612600-9615800	Active TSS	Aorta	Aorta
15	chr18:9612800-9615000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr18:9612800-9615200	Active TSS	Fetal Muscle Leg	muscle
17	chr18:9612800-9615200	Active TSS	HSMM	muscle
18	chr18:9612800-9615200	Active TSS	HSMMtube	muscle
19	chr18:9612800-9615200	Active TSS	NHDF-Ad	bronchial
20	chr18:9612800-9615400	Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr18:9612800-9615400	Active TSS	A549	lung
22	chr18:9612800-9615600	Active TSS	ES-I3 Cell Line	embryonic stem cell
23	chr18:9613000-9615200	Active TSS	H1 Cell Line	embryonic stem cell
24	chr18:9613000-9615200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr18:9613000-9615200	Active TSS	Fetal Stomach	stomach
26	chr18:9613000-9615400	Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr18:9613000-9615600	Active TSS	Fetal Brain Female	brain
28	chr18:9613200-9614200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
29	chr18:9613200-9614200	Active TSS	Fetal Lung	lung
30	chr18:9613200-9615000	Active TSS	K562	blood
31	chr18:9613200-9615200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr18:9613200-9615200	Active TSS	HUES64 Cell Line	embryonic stem cell
33	chr18:9613200-9615200	Active TSS	iPS-18 Cell Line	embryonic stem cell
34	chr18:9613200-9615200	Active TSS	Brain Cingulate Gyrus	brain
35	chr18:9613200-9615200	Active TSS	Brain Hippocampus Middle	brain
36	chr18:9613200-9615200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
37	chr18:9613200-9615200	Active TSS	Brain Substantia Nigra	brain
38	chr18:9613200-9615200	Active TSS	Colonic Mucosa	Colon
39	chr18:9613200-9615200	Active TSS	Fetal Intestine Small	intestine
40	chr18:9613200-9615200	Active TSS	Placenta	Placenta
41	chr18:9613200-9615200	Active TSS	Fetal Thymus	thymus
42	chr18:9613200-9615200	Active TSS	Stomach Smooth Muscle	stomach
43	chr18:9613200-9615200	Active TSS	NHEK	skin
44	chr18:9613200-9615400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr18:9613200-9615400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr18:9613200-9615400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr18:9613200-9615400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr18:9613200-9615400	Active TSS	Colon Smooth Muscle	Colon
49	chr18:9613200-9615400	Active TSS	Fetal Intestine Large	intestine
50	chr18:9613200-9615600	Active TSS	Pancreatic Islets	Pancreatic Islet

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