Variant report

Variant	nsv978798
Chromosome Location	chr19:24261622-24285690
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:461)
CpG islands
(count:368)
Chromatin interactive
region (count:23)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:461 , 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	chr19:24277965-24278090	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:24269634-24269992	K562	blood:	n/a	n/a
3	ATF1	chr19:24269666-24270047	K562	blood:	n/a	n/a
4	ATF2	chr19:24269632-24269953	GM12878	blood:	n/a	n/a
5	BACH1	chr19:24270502-24270514	K562	blood:	n/a	n/a
6	BCL3	chr19:24269789-24270455	GM12878	blood:	n/a	n/a
7	BCL3	chr19:24269688-24270514	A549	lung:	n/a	n/a
8	BCL3	chr19:24269800-24270463	A549	lung:	n/a	n/a
9	BCLAF1	chr19:24269773-24270344	GM12878	blood:	n/a	n/a
10	BHLHE40	chr19:24269821-24270044	K562	blood:	n/a	n/a
11	CBX3	chr19:24269975-24270349	K562	blood:	n/a	n/a
12	CEBPB	chr19:24274254-24274360	K562	blood:	n/a	n/a
13	CEBPB	chr19:24269821-24270021	A549	lung:	n/a	n/a
14	CEBPB	chr19:24269746-24270087	K562	blood:	n/a	n/a
15	CEBPB	chr19:24262715-24262748	A549	lung:	n/a	n/a
16	CEBPB	chr19:24268405-24268573	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr19:24269699-24270116	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr19:24270144-24270151	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr19:24268418-24268618	K562	blood:	n/a	n/a
20	CEBPB	chr19:24269736-24270125	K562	blood:	n/a	n/a
21	CEBPD	chr19:24269764-24270215	K562	blood:	n/a	n/a
22	CEBPD	chr19:24269710-24270404	K562	blood:	n/a	n/a
23	CHD1	chr19:24269530-24270611	IMR90	lung:	n/a	n/a
24	CHD1	chr19:24270004-24270498	GM12878	blood:	n/a	n/a
25	CHD2	chr19:24269818-24270242	K562	blood:	n/a	n/a
26	CHD2	chr19:24269745-24270337	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr19:24269829-24270027	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr19:24269727-24270371	GM12878	blood:	n/a	n/a
29	CREB1	chr19:24269797-24270053	A549	lung:	n/a	n/a
30	CREB1	chr19:24269696-24270445	A549	lung:	n/a	n/a
31	CTCF	chr19:24270260-24270410	AG09319	gingival:	n/a	n/a
32	CTCF	chr19:24270047-24270090	MCF-7	breast:	n/a	chr19:24270081-24270089
33	CTCF	chr19:24270160-24270310	HCM	heart:	n/a	n/a
34	CTCF	chr19:24270240-24270390	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr19:24270220-24270370	AG09309	skin:	n/a	n/a
36	CTCF	chr19:24270010-24270115	MCF-7	breast:	n/a	chr19:24270081-24270089
37	CTCF	chr19:24270160-24270310	HVMF	connective:	n/a	n/a
38	CTCF	chr19:24270062-24270085	MCF-7	breast:	n/a	n/a
39	CTCF	chr19:24270300-24270450	HPF	lung:	n/a	n/a
40	CTCF	chr19:24270220-24270370	GM12864	blood:	n/a	n/a
41	CTCF	chr19:24270240-24270390	HCFaa	heart:	n/a	n/a
42	CTCF	chr19:24270240-24270390	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr19:24270260-24270410	GM06990	blood:	n/a	n/a
44	CTCF	chr19:24270328-24270348	MCF-7	breast:	n/a	n/a
45	CTCF	chr19:24270200-24270350	AG04449	skin:	n/a	n/a
46	CTCF	chr19:24270300-24270450	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr19:24270326-24270350	MCF-7	breast:	n/a	n/a
48	CTCF	chr19:24270200-24270350	SAEC	small airway:	n/a	n/a
49	CTCF	chr19:24270340-24270490	HAc	cerebellar:	n/a	n/a
50	CTCF	chr19:24270300-24270450	AoAF	blood vessel:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:24270007-24270057	HRPEpiC	eye:	n/a
2	chr19:24269890-24269940	CMK	blood:	n/a
3	chr19:24270007-24270057	HRPEpiC	eye:	n/a
4	chr19:24269890-24269940	CMK	blood:	n/a
5	chr19:24270007-24270057	Hepatocyte	liver:	n/a
6	chr19:24269890-24269940	HIPEpiC	eye:	n/a
7	chr19:24269975-24270025	NHDF-neo	bronchial:	n/a
8	chr19:24269975-24270025	Hepatocyte	liver:	n/a
9	chr19:24270073-24270123	GM06990	blood:	n/a
10	chr19:24270007-24270057	BJ	skin:	n/a
11	chr19:24270073-24270123	BJ	skin:	n/a
12	chr19:24270468-24270518	T-47D	breast:	n/a
13	chr19:24270007-24270057	GM12892	blood:	n/a
14	chr19:24269968-24270018	LNCaP	prostate:	n/a
15	chr19:24270468-24270518	HCF	heart:	n/a
16	chr19:24269968-24270018	A549	lung:	n/a
17	chr19:24269968-24270018	BE2_C	brain:	n/a
18	chr19:24270073-24270123	HCPEpiC	choroid plexus:	n/a
19	chr19:24270468-24270518	AG04450	lung:	fetal
20	chr19:24269890-24269940	HCF	heart:	n/a
21	chr19:24270073-24270123	HMEC	breast:	n/a
22	chr19:24269968-24270018	AG09319	gingival:	n/a
23	chr19:24270007-24270057	SK-N-SH_RA	brain:	n/a
24	chr19:24270073-24270123	AG09309	skin:	n/a
25	chr19:24269975-24270025	SAEC	small airway:	n/a
26	chr19:24270073-24270123	HepG2	liver:	n/a
27	chr19:24269890-24269940	AoSMC	blood vessel:	n/a
28	chr19:24269975-24270025	SK-N-SH	brain:	n/a
29	chr19:24269890-24269940	H1-hESC	embryonic stem cell:	embryo
30	chr19:24269890-24269940	SKMC	muscle:	n/a
31	chr19:24269968-24270018	HAEpiC	amniotic membrane:	n/a
32	chr19:24270073-24270123	HRCEpiC	kidney:	n/a
33	chr19:24269968-24270018	NH-A	brain:	n/a
34	chr19:24269968-24270018	AG09309	skin:	n/a
35	chr19:24269968-24270018	AG04450	lung:	fetal
36	chr19:24269968-24270018	PANC-1	pancreas:	n/a
37	chr19:24270468-24270518	HCPEpiC	choroid plexus:	n/a
38	chr19:24270007-24270057	LNCaP	prostate:	n/a
39	chr19:24270468-24270518	SK-N-MC	brain:	n/a
40	chr19:24270073-24270123	ovcar-3	ovarian:	n/a
41	chr19:24270468-24270518	PANC-1	pancreas:	n/a
42	chr19:24269968-24270018	HNPCEpiC	eye:	n/a
43	chr19:24269890-24269940	NHDF-neo	bronchial:	n/a
44	chr19:24269890-24269940	AG04450	lung:	fetal
45	chr19:24270468-24270518	NB4	blood:	n/a
46	chr19:24270007-24270057	T-47D	breast:	n/a
47	chr19:24269890-24269940	HMEC	breast:	n/a
48	chr19:24269975-24270025	GM12878	blood:	n/a
49	chr19:24270007-24270057	H1-hESC	embryonic stem cell:	embryo
50	chr19:24270468-24270518	SK-N-SH	brain:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:24269905..24270406-chr19:47616316..47616816,2	Hela-S3	cervix:
2	chr19:24259633..24261954-chr19:24264243..24265870,2	K562	blood:
3	chr19:24214637..24216513-chr19:24268176..24271021,2	K562	blood:
4	chr19:23299713..23300295-chr19:24269911..24270643,3	Hela-S3	cervix:
5	chr19:24269855..24272221-chr19:24274367..24277034,2	K562	blood:
6	chr19:24216492..24217018-chr19:24270056..24270717,2	Hela-S3	cervix:
7	chr19:24273653..24275947-chr19:24283763..24286065,2	K562	blood:
8	chr19:24216051..24217841-chr19:24269020..24271219,2	MCF-7	breast:
9	chr19:24278737..24281409-chr19:24289986..24291875,2	K562	blood:
10	chr19:24264646..24268309-chr19:24268403..24270705,3	MCF-7	breast:
11	chr19:24214690..24216513-chr19:24269521..24272423,2	K562	blood:
12	chr19:24253983..24255588-chr19:24260053..24261773,2	K562	blood:
13	chr19:24097706..24100500-chr19:24267529..24270344,3	K562	blood:
14	chr19:24269806..24272597-chr19:24274053..24277432,4	K562	blood:
15	chr19:24266915..24268889-chr19:24271542..24273329,2	MCF-7	breast:
16	chr19:24269869..24271737-chr19:24281128..24282836,2	MCF-7	breast:
17	chr19:24266915..24268889-chr19:24271542..24273329,2	MCF-7	breast:
18	chr19:24259633..24261954-chr19:24264243..24265870,2	K562	blood:
19	chr19:24269191..24271795-chr19:24273714..24276847,3	MCF-7	breast:
20	chr19:24269481..24270366-chr8:29940201..29940789,2	NB4	blood:
21	chr19:24273653..24275947-chr19:24283763..24286065,2	K562	blood:
22	chr19:24269801..24271346-chr19:24277835..24280239,2	K562	blood:
23	chr19:24269869..24271737-chr19:24281128..24282836,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF681-5	chr19:24281227-24281782	NONHSAT063956

No data

Variant related genes	Relation type
ENSG00000268058	TF binding region
ZNF254	TF binding region
ENSG00000268058	CpG island
ZNF254	CpG island
ENSG00000142230	chromatin interactions
ENSG00000268362	chromatin interactions
ENSG00000268058	chromatin interactions
ENSG00000272256	chromatin interactions
ENSG00000213096	chromatin interactions
ENSG00000213967	chromatin interactions
ENSG00000133872	chromatin interactions
ENSG00000183850	chromatin interactions

Extended variants
information (count: 840 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:840 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530816834	chr19:24261641-24261642	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs7507208	chr19:24261686-24261687	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs567301310	chr19:24261698-24261699	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs114598281	chr19:24261700-24261701	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs182180242	chr19:24261732-24261733	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs185879202	chr19:24261733-24261734	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs571240409	chr19:24261739-24261740	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs538280387	chr19:24261743-24261744	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs190203154	chr19:24261813-24261814	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs569253786	chr19:24261835-24261836	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs536547683	chr19:24261846-24261847	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs554748003	chr19:24261847-24261848	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs182528856	chr19:24261854-24261855	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs367993094	chr19:24261935-24261936	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs558754146	chr19:24261937-24261938	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs188670481	chr19:24261990-24261991	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs60976011	chr19:24262006-24262007	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs141728227	chr19:24262119-24262120	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs34881248	chr19:24262125-24262126	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs34227383	chr19:24262179-24262180	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs530827933	chr19:24262192-24262193	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs542900861	chr19:24262222-24262223	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs35538487	chr19:24262258-24262259	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370738138	chr19:24262284-24262285	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs117825292	chr19:24262325-24262326	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546748694	chr19:24262353-24262354	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564861448	chr19:24262449-24262450	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532071189	chr19:24262516-24262517	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550210928	chr19:24262548-24262549	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs58934785	chr19:24262551-24262552	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs536558822	chr19:24262598-24262599	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550799668	chr19:24262645-24262646	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531458932	chr19:24262664-24262665	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs118041058	chr19:24262737-24262738	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147100973	chr19:24262768-24262769	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192849028	chr19:24262784-24262785	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs151114432	chr19:24262809-24262810	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564900394	chr19:24262824-24262825	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577313018	chr19:24262857-24262858	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113325043	chr19:24262878-24262879	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532322215	chr19:24262897-24262898	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539464637	chr19:24262916-24262917	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35075460	chr19:24262949-24262950	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552922896	chr19:24262959-24262960	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141104279	chr19:24262960-24262961	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150076137	chr19:24262968-24262969	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs6511683	chr19:24263003-24263004	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs138388356	chr19:24263015-24263016	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs565767813	chr19:24263018-24263019	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs184111282	chr19:24263043-24263044	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:44)

Disease	PMID	Source
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:961 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:24236200-24269400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr19:24239800-24269600	Weak transcription	Small Intestine	intestine
3	chr19:24242000-24269800	Weak transcription	Stomach Mucosa	stomach
4	chr19:24242400-24269400	Weak transcription	Fetal Thymus	thymus
5	chr19:24243600-24269600	Weak transcription	NHLF	lung
6	chr19:24244200-24269400	Weak transcription	HUVEC	blood vessel
7	chr19:24245200-24270000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr19:24250200-24269200	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr19:24251000-24269400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr19:24251200-24269200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr19:24251200-24269600	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr19:24251200-24269800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr19:24251400-24269600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr19:24251600-24269600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr19:24251600-24269600	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr19:24251800-24269000	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr19:24251800-24269400	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr19:24252600-24263400	Strong transcription	Liver	Liver
19	chr19:24255800-24269600	Weak transcription	Osteobl	bone
20	chr19:24256200-24269600	Weak transcription	Rectal Smooth Muscle	rectum
21	chr19:24256200-24269600	Weak transcription	HSMM	muscle
22	chr19:24256600-24269600	Weak transcription	NHDF-Ad	bronchial
23	chr19:24256600-24269800	Weak transcription	Colon Smooth Muscle	Colon
24	chr19:24256800-24269600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr19:24256800-24270000	Weak transcription	Fetal Brain Male	brain
26	chr19:24257000-24263000	Weak transcription	Brain Germinal Matrix	brain
27	chr19:24257000-24269400	Weak transcription	Brain Hippocampus Middle	brain
28	chr19:24257000-24269400	Weak transcription	Pancreas	Pancrea
29	chr19:24257000-24269600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr19:24257000-24269800	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr19:24257000-24270000	Weak transcription	Aorta	Aorta
32	chr19:24257200-24269200	Weak transcription	Primary B cells from peripheral blood	blood
33	chr19:24257200-24269400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr19:24257200-24269800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr19:24257400-24269400	Weak transcription	Thymus	Thymus
36	chr19:24257400-24269600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr19:24257400-24269800	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr19:24257400-24269800	Weak transcription	Ovary	ovary
39	chr19:24257400-24270000	Weak transcription	Gastric	stomach
40	chr19:24257600-24263200	Weak transcription	Spleen	Spleen
41	chr19:24257600-24269400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr19:24257600-24269400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr19:24257600-24269400	Weak transcription	Adipose Nuclei	Adipose
44	chr19:24257600-24269400	Weak transcription	Duodenum Mucosa	Duodenum
45	chr19:24257600-24269400	Weak transcription	Lung	lung
46	chr19:24257600-24269400	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr19:24257600-24269400	Weak transcription	Hela-S3	cervix
48	chr19:24257600-24269600	Weak transcription	HMEC	breast
49	chr19:24257800-24269200	Weak transcription	Primary B cells from cord blood	blood
50	chr19:24257800-24269600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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