Variant report

Variant	nsv909528
Chromosome Location	chr18:30875118-31011926
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:353)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:30979348-30979502	K562	blood:	n/a	n/a
2	ARID3A	chr18:31001047-31001058	K562	blood:	n/a	n/a
3	ATF1	chr18:31003250-31003295	K562	blood:	n/a	n/a
4	CEBPB	chr18:30907026-30907322	H1-hESC	embryonic stem cell:	n/a	chr18:30907159-30907170
5	CEBPB	chr18:31010187-31010454	K562	blood:	n/a	n/a
6	CEBPB	chr18:30907016-30907332	A549	lung:	n/a	chr18:30907159-30907170
7	CEBPB	chr18:30954573-30954887	HepG2	liver:	n/a	chr18:30954714-30954725
8	CEBPB	chr18:30902685-30902878	HepG2	liver:	n/a	chr18:30902705-30902716 chr18:30902766-30902779 chr18:30902767-30902778
9	CEBPB	chr18:30904175-30904423	A549	lung:	n/a	chr18:30904334-30904343 chr18:30904332-30904343 chr18:30904334-30904343 chr18:30904334-30904345 chr18:30904332-30904345 chr18:30904334-30904343 chr18:30904334-30904343
10	CEBPB	chr18:30906979-30907352	K562	blood:	n/a	chr18:30907159-30907170
11	CEBPB	chr18:30906968-30907317	HepG2	liver:	n/a	chr18:30907159-30907170
12	CEBPB	chr18:30911883-30912106	HepG2	liver:	n/a	chr18:30911978-30911989
13	CEBPB	chr18:30904181-30904489	HepG2	liver:	n/a	chr18:30904334-30904343 chr18:30904332-30904343 chr18:30904334-30904343 chr18:30904334-30904345 chr18:30904332-30904345 chr18:30904334-30904343 chr18:30904334-30904343
14	CEBPB	chr18:30906913-30907355	ECC-1	luminal epithelium:	n/a	chr18:30907159-30907170
15	CEBPB	chr18:30999949-31000048	HepG2	liver:	n/a	n/a
16	CEBPB	chr18:30906973-30907362	ECC-1	luminal epithelium:	n/a	chr18:30907159-30907170
17	CEBPB	chr18:30906969-30907351	Hela-S3	cervix:	n/a	chr18:30907159-30907170
18	CHD2	chr18:30896393-30896593	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr18:30984300-30984450	HPF	lung:	n/a	n/a
20	CTCF	chr18:30984285-30984432	GM10248	blood:	n/a	n/a
21	CTCF	chr18:30913140-30913290	HEK293	kidney:	n/a	n/a
22	CTCF	chr18:30984120-30984270	SAEC	small airway:	n/a	n/a
23	CTCF	chr18:30913120-30913270	NHEK	skin:	n/a	n/a
24	CTCF	chr18:30984360-30984510	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr18:30984340-30984490	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr18:30960040-30960190	GM12867	blood:	n/a	n/a
27	CTCF	chr18:30984220-30984370	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr18:30896400-30896550	GM12871	blood:	n/a	n/a
29	CTCF	chr18:30913160-30913310	HMEC	breast:	n/a	n/a
30	CTCF	chr18:30896320-30896470	GM12870	blood:	n/a	n/a
31	CTCF	chr18:30986880-30987030	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr18:30896397-30896570	K562	blood:	n/a	n/a
33	CTCF	chr18:30913160-30913310	RPTEC	kidney:	n/a	n/a
34	CTCF	chr18:30984318-30984460	K562	blood:	n/a	n/a
35	CTCF	chr18:30984340-30984490	HCFaa	heart:	n/a	n/a
36	CTCF	chr18:30986960-30987110	HRE	kidney:	n/a	n/a
37	CTCF	chr18:30913116-30913278	LNCaP	prostate:	n/a	n/a
38	CTCF	chr18:30984300-30984450	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr18:30984300-30984450	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr18:30896357-30896568	HepG2	liver:	n/a	n/a
41	CTCF	chr18:30984260-30984410	AG09319	gingival:	n/a	n/a
42	CTCF	chr18:30913060-30913210	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr18:30935900-30936050	MCF-7	breast:	n/a	n/a
44	CTCF	chr18:30984320-30984470	NHEK	skin:	n/a	n/a
45	CTCF	chr18:30984305-30984461	GM13977	blood:	n/a	n/a
46	CTCF	chr18:30984320-30984470	HMEC	breast:	n/a	n/a
47	CTCF	chr18:30913140-30913290	MCF-7	breast:	n/a	n/a
48	CTCF	chr18:30984340-30984490	HPF	lung:	n/a	n/a
49	CTCF	chr18:30984120-30984270	HAc	cerebellar:	n/a	n/a
50	CTCF	chr18:30896360-30896510	GM12865	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:30896376-30896426	U87	brain:	n/a
2	chr18:30896376-30896426	SK-N-MC	brain:	n/a
3	chr18:30896376-30896426	LNCaP	prostate:	n/a
4	chr18:30896376-30896426	AG04449	skin:	fetal
5	chr18:30896376-30896426	HAEpiC	amniotic membrane:	n/a
6	chr18:30896376-30896426	T-47D	breast:	n/a
7	chr18:30896376-30896426	ECC-1	luminal epithelium:	n/a
8	chr18:30896376-30896426	HEK293	kidney:	embryo
9	chr18:30896376-30896426	AoSMC	blood vessel:	n/a
10	chr18:30896376-30896426	HUVEC	blood vessel:	n/a
11	chr18:30896376-30896426	IMR90	lung:	fetal
12	chr18:30896376-30896426	HCPEpiC	choroid plexus:	n/a
13	chr18:30896376-30896426	HCM	heart:	n/a
14	chr18:30896376-30896426	HEEpiC	esophagus:	n/a
15	chr18:30896376-30896426	NT2-D1	testis:	n/a
16	chr18:30896376-30896426	MCF10A-Er-Src	breast:	n/a
17	chr18:30896376-30896426	PFSK-1	brain:	n/a
18	chr18:30896376-30896426	NHDF-neo	bronchial:	n/a
19	chr18:30896376-30896426	HepG2	liver:	n/a
20	chr18:30896376-30896426	AG10803	skin:	n/a
21	chr18:30896376-30896426	NHBE	bronchial:	n/a
22	chr18:30896376-30896426	HPAEpiC	pulmonary alveolar:	n/a
23	chr18:30896376-30896426	HL-60	blood:	n/a
24	chr18:30896376-30896426	SK-N-SH	brain:	n/a
25	chr18:30896376-30896426	H1-hESC	embryonic stem cell:	embryo
26	chr18:30896376-30896426	ovcar-3	ovarian:	n/a
27	chr18:30896376-30896426	PrEC	prostate:	n/a
28	chr18:30896376-30896426	HCT-116	colon:	n/a
29	chr18:30896376-30896426	RPTEC	kidney:	n/a
30	chr18:30896376-30896426	PANC-1	pancreas:	n/a
31	chr18:30896376-30896426	HRE	kidney:	n/a
32	chr18:30896376-30896426	SKMC	muscle:	n/a
33	chr18:30896376-30896426	HMEC	breast:	n/a
34	chr18:30896376-30896426	HRPEpiC	eye:	n/a
35	chr18:30896376-30896426	NB4	blood:	n/a
36	chr18:30896376-30896426	GM19239	blood:	n/a
37	chr18:30896376-30896426	Jurkat	blood:	n/a
38	chr18:30896376-30896426	BJ	skin:	n/a
39	chr18:30896376-30896426	Hepatocyte	liver:	n/a
40	chr18:30896376-30896426	BE2_C	brain:	n/a
41	chr18:30896376-30896426	HCF	heart:	n/a
42	chr18:30896376-30896426	K562	blood:	n/a
43	chr18:30896376-30896426	HIPEpiC	eye:	n/a
44	chr18:30896376-30896426	GM12878	blood:	n/a
45	chr18:30896376-30896426	A549	lung:	n/a
46	chr18:30896376-30896426	GM06990	blood:	n/a
47	chr18:30896376-30896426	AG04450	lung:	fetal
48	chr18:30896376-30896426	Hela-S3	cervix:	n/a
49	chr18:30896376-30896426	GM12891	blood:	n/a
50	chr18:30896376-30896426	SAEC	small airway:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:30931078..30933531-chr18:30935851..30938353,2	K562	blood:
2	chr18:31004069..31006377-chr18:31011113..31013789,2	K562	blood:
3	chr18:30983983..30984636-chr18:31075029..31075877,2	MCF-7	breast:
4	chr18:31004069..31006377-chr18:31011113..31013789,2	K562	blood:
5	chr18:31003864..31006821-chr18:31008569..31010754,2	K562	blood:
6	chr18:31011782..31014232-chr18:31017027..31018829,2	K562	blood:
7	chr18:31003864..31006821-chr18:31008569..31010754,2	K562	blood:
8	chr18:30984281..30985094-chr18:31340995..31341589,3	MCF-7	breast:
9	chr18:30984084..30985234-chr18:31075317..31075966,4	MCF-7	breast:
10	chr18:30931078..30933531-chr18:30935851..30938353,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASXL3-2	chr18:30976632-30977116	expReg_chr18_1719_+

No data

Variant related genes	Relation type
CCDC178	TF binding region
CCDC178	CpG island

Extended variants
information (count: 1287 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1287 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149841137	chr18:30877206-30877207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs183410146	chr18:30877233-30877234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570709087	chr18:30877236-30877237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573548648	chr18:30877247-30877248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539675265	chr18:30877319-30877320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540943010	chr18:30877366-30877367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556427461	chr18:30877450-30877451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570030832	chr18:30877500-30877501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374410736	chr18:30877545-30877546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568053580	chr18:30877546-30877547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565294356	chr18:30877579-30877580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7227131	chr18:30877595-30877596	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs543970218	chr18:30877638-30877639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540311718	chr18:30877642-30877643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553956478	chr18:30877733-30877734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7227288	chr18:30877734-30877735	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs546052767	chr18:30877744-30877745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7227315	chr18:30877790-30877791	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs531639143	chr18:30877801-30877802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556109563	chr18:30877821-30877822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562104993	chr18:30877867-30877868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs527732156	chr18:30877874-30877875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547466583	chr18:30877899-30877900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372028398	chr18:30877921-30877922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575034874	chr18:30877923-30877924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7231699	chr18:30877948-30877949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370611366	chr18:30877955-30877956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559741534	chr18:30877959-30877960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560613385	chr18:30877977-30877978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147586080	chr18:30877983-30877984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374078655	chr18:30877988-30877989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536154805	chr18:30878005-30878006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75299485	chr18:30878006-30878007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527915908	chr18:30878036-30878037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142216078	chr18:30878082-30878083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188833503	chr18:30878091-30878092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533797912	chr18:30878096-30878097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527551024	chr18:30878097-30878098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536624175	chr18:30878129-30878130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145957861	chr18:30878171-30878172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs8182395	chr18:30878191-30878192	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs148235564	chr18:30878254-30878255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556403774	chr18:30878262-30878263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576199792	chr18:30878306-30878307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564186703	chr18:30878346-30878347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556655956	chr18:30878369-30878370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370856941	chr18:30878370-30878371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561862463	chr18:30878373-30878374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538083243	chr18:30878427-30878428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572391987	chr18:30878458-30878459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Glioblastoma multiforme	21922591	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	21811587	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	19181860	CNVD

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30877200-30880400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr18:30880400-30880800	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr18:30880400-30881200	Enhancers	H9 Cell Line	embryonic stem cell
4	chr18:30880400-30881200	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr18:30881000-30881600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr18:30884600-30885200	Enhancers	Fetal Lung	lung
7	chr18:30895800-30896000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
8	chr18:30895800-30896600	Active TSS	H1 Cell Line	embryonic stem cell
9	chr18:30896000-30896200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr18:30896000-30896600	Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr18:30896200-30896400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr18:30896200-30898200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr18:30896400-30896600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr18:30898200-30898400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr18:30910400-30912200	Enhancers	Fetal Lung	lung
16	chr18:30912600-30912800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr18:30935200-30935800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr18:30935200-30936800	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr18:30935200-30937200	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr18:30935200-30937200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr18:30935200-30937200	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr18:30935400-30936600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr18:30935400-30937600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr18:30935400-30937600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr18:30935600-30936000	Enhancers	H9 Cell Line	embryonic stem cell
26	chr18:30935600-30937200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr18:30936400-30936800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr18:30952200-30953000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr18:30958400-30962400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr18:30962400-30962800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr18:30963400-30963800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr18:30975000-30976000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr18:30975200-30975400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr18:30975400-30975600	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr18:30975600-30975800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr18:30975600-30975800	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr18:30975600-30975800	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr18:30975600-30976600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr18:30975600-30976600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr18:30975800-30976800	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr18:30975800-30976800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr18:30976000-30976400	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr18:30976000-30977200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr18:30976400-30977800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr18:30976600-30977600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr18:30976600-30977800	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr18:30976600-30977800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr18:30976600-30977800	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr18:30976800-30977600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr18:30976800-30977800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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