Variant report

Variant	esv3408235
Chromosome Location	chr19:42396537-42399085
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr19:42397984-42398446	A549	lung:	n/a	n/a
2	CBX3	chr19:42397988-42398335	K562	blood:	n/a	n/a
3	CCNT2	chr19:42396842-42396848	K562	blood:	n/a	n/a
4	CEBPB	chr19:42397898-42398262	HepG2	liver:	n/a	n/a
5	CEBPB	chr19:42397982-42398244	HepG2	liver:	n/a	n/a
6	CEBPD	chr19:42398058-42398314	HepG2	liver:	n/a	n/a
7	CHD2	chr19:42398118-42398277	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr19:42398063-42398418	A549	lung:	n/a	n/a
9	CTCF	chr19:42397842-42398859	A549	lung:	n/a	chr19:42398170-42398188
10	CTCF	chr19:42398056-42398322	H1-hESC	embryonic stem cell:	n/a	chr19:42398170-42398188
11	CTCF	chr19:42398040-42398190	HMF	breast:	n/a	chr19:42398170-42398188
12	CTCF	chr19:42398060-42398210	NB4	blood:	n/a	chr19:42398170-42398188
13	CTCF	chr19:42398040-42398190	SAEC	small airway:	n/a	chr19:42398170-42398188
14	CTCF	chr19:42398220-42398370	A549	lung:	n/a	n/a
15	CTCF	chr19:42397977-42398372	K562	blood:	n/a	chr19:42398170-42398188
16	CTCF	chr19:42398070-42398303	HepG2	liver:	n/a	chr19:42398170-42398188
17	CTCF	chr19:42398060-42398210	HAc	cerebellar:	n/a	chr19:42398170-42398188
18	CTCF	chr19:42398040-42398190	WERI-Rb-1	eye:	n/a	chr19:42398170-42398188
19	CTCF	chr19:42398040-42398190	HEK293	kidney:	n/a	chr19:42398170-42398188
20	CTCF	chr19:42398040-42398190	HCM	heart:	n/a	chr19:42398170-42398188
21	CTCF	chr19:42398040-42398190	HCPEpiC	choroid plexus:	n/a	chr19:42398170-42398188
22	CTCF	chr19:42398020-42398170	NHLF	lung:	n/a	n/a
23	CTCF	chr19:42398076-42398346	MCF-7	breast:	n/a	chr19:42398170-42398188
24	CTCF	chr19:42398040-42398190	GM12874	blood:	n/a	chr19:42398170-42398188
25	CTCF	chr19:42398090-42398265	GM19240	blood:	n/a	chr19:42398170-42398188
26	CTCF	chr19:42398120-42398270	GM12872	blood:	n/a	chr19:42398170-42398188
27	CTCF	chr19:42398131-42398168	GM13976	blood:	n/a	n/a
28	CTCF	chr19:42398103-42398275	Hela-S3	cervix:	n/a	chr19:42398170-42398188
29	CTCF	chr19:42398120-42398270	RPTEC	kidney:	n/a	chr19:42398170-42398188
30	CTCF	chr19:42397993-42398294	A549	lung:	n/a	chr19:42398170-42398188
31	CTCF	chr19:42398100-42398250	HCPEpiC	choroid plexus:	n/a	chr19:42398170-42398188
32	CTCF	chr19:42398090-42398294	Gliobla	brain:	n/a	chr19:42398170-42398188
33	CTCF	chr19:42398080-42398288	GM12878	blood:	n/a	chr19:42398170-42398188
34	CTCF	chr19:42398240-42398390	HFF	foreskin:	n/a	n/a
35	CTCF	chr19:42398080-42398230	GM12869	blood:	n/a	chr19:42398170-42398188
36	CTCF	chr19:42398120-42398270	HepG2	liver:	n/a	chr19:42398170-42398188
37	CTCF	chr19:42398100-42398240	GM10266	blood:	n/a	chr19:42398170-42398188
38	CTCF	chr19:42398060-42398210	GM12868	blood:	n/a	chr19:42398170-42398188
39	CTCF	chr19:42398040-42398190	GM06990	blood:	n/a	chr19:42398170-42398188
40	CTCF	chr19:42398060-42398331	MCF-7	breast:	n/a	chr19:42398170-42398188
41	CTCF	chr19:42398120-42398270	GM12865	blood:	n/a	chr19:42398170-42398188
42	CTCF	chr19:42398040-42398190	GM12872	blood:	n/a	chr19:42398170-42398188
43	CTCF	chr19:42398072-42398304	MCF-7	breast:	n/a	chr19:42398170-42398188
44	CTCF	chr19:42398141-42398181	ProgFib	skin:	n/a	n/a
45	CTCF	chr19:42398100-42398250	HPF	lung:	n/a	chr19:42398170-42398188
46	CTCF	chr19:42398140-42398290	GM12865	blood:	n/a	chr19:42398170-42398188
47	CTCF	chr19:42398080-42398230	HVMF	connective:	n/a	chr19:42398170-42398188
48	CTCF	chr19:42398040-42398190	HUVEC	blood vessel:	n/a	chr19:42398170-42398188
49	CTCF	chr19:42398100-42398250	AoAF	blood vessel:	n/a	chr19:42398170-42398188
50	CTCF	chr19:42398160-42398310	GM12870	blood:	n/a	chr19:42398170-42398188

No.	Distal block	Cell Line	Cell type
1	chr19:42397636..42399907-chr19:42401318..42404591,3	K562	blood:
2	chr19:42386993..42388717-chr19:42395011..42397502,2	K562	blood:
3	chr19:42398480..42400174-chr19:42432062..42434996,2	K562	blood:
4	chr19:42385266..42389164-chr19:42392215..42397025,5	MCF-7	breast:
5	chr19:42398848..42401100-chr19:42409902..42411983,2	MCF-7	breast:

Variant related genes	Relation type
ARHGEF1	TF binding region
ENSG00000076928	chromatin interactions

Extended variants
information (count: 176 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:176 , 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	rs566159951	chr19:42396540-42396541	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs551980953	chr19:42396547-42396548	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs149447500	chr19:42396584-42396585	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs529138487	chr19:42396617-42396618	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs537441393	chr19:42396628-42396629	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs201239583	chr19:42396636-42396637	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs374142786	chr19:42396654-42396655	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs369826806	chr19:42396676-42396677	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs554668510	chr19:42396699-42396700	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs373367437	chr19:42396711-42396712	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs376815607	chr19:42396716-42396717	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs368913647	chr19:42396721-42396722	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs576022348	chr19:42396758-42396759	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs200573860	chr19:42396761-42396762	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs372670738	chr19:42396771-42396772	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs199623203	chr19:42396785-42396786	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs577018777	chr19:42396864-42396865	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs193119387	chr19:42396877-42396878	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs367971459	chr19:42396882-42396883	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs529943853	chr19:42396887-42396888	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs185786994	chr19:42396943-42396944	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs3815956	chr19:42396947-42396948	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs371762884	chr19:42396953-42396954	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs530633084	chr19:42396970-42396971	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs190312067	chr19:42396973-42396974	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs552106853	chr19:42396974-42396975	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs563950113	chr19:42396975-42396976	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs182142459	chr19:42397001-42397002	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs547812956	chr19:42397088-42397089	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs565911320	chr19:42397137-42397138	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs143868598	chr19:42397177-42397178	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs113284840	chr19:42397179-42397180	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs531829768	chr19:42397183-42397184	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs148598286	chr19:42397227-42397228	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs569772424	chr19:42397237-42397238	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs537151817	chr19:42397270-42397271	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs202168122	chr19:42397273-42397274	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs558882193	chr19:42397304-42397305	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs373399447	chr19:42397316-42397317	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs577184053	chr19:42397326-42397327	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs201258313	chr19:42397329-42397330	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs200700417	chr19:42397336-42397337	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs202211558	chr19:42397339-42397340	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs371827282	chr19:42397379-42397380	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs374431812	chr19:42397381-42397382	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs372121595	chr19:42397398-42397399	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs199564457	chr19:42397399-42397400	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs376783154	chr19:42397408-42397409	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs142963850	chr19:42397411-42397412	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs147308449	chr19:42397430-42397431	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	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
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD

Chromatin state (count:207 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42389200-42407200	Weak transcription	Fetal Kidney	kidney
2	chr19:42389200-42429200	Weak transcription	Right Atrium	heart
3	chr19:42389400-42398200	Weak transcription	Colon Smooth Muscle	Colon
4	chr19:42389400-42402000	Weak transcription	Psoas Muscle	Psoas
5	chr19:42389400-42406000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr19:42389400-42411400	Weak transcription	Fetal Brain Male	brain
7	chr19:42389800-42409000	Strong transcription	Fetal Stomach	stomach
8	chr19:42390800-42411200	Weak transcription	Hela-S3	cervix
9	chr19:42391400-42396800	Weak transcription	Brain Anterior Caudate	brain
10	chr19:42391400-42407400	Weak transcription	K562	blood
11	chr19:42391600-42399600	Weak transcription	HUVEC	blood vessel
12	chr19:42391600-42404600	Weak transcription	HSMM	muscle
13	chr19:42392000-42399600	Strong transcription	Lung	lung
14	chr19:42392000-42404000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr19:42392000-42412600	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr19:42392000-42412600	Strong transcription	Cortex derived primary cultured neurospheres	brain
17	chr19:42392000-42412600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr19:42392200-42397400	Strong transcription	Muscle Satellite Cultured Cells	--
19	chr19:42392200-42400800	Strong transcription	Skeletal Muscle Male	skeletal muscle
20	chr19:42392200-42401400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr19:42392200-42407600	Strong transcription	Sigmoid Colon	Sigmoid Colon
22	chr19:42392200-42408400	Strong transcription	Liver	Liver
23	chr19:42392200-42412400	Strong transcription	Fetal Muscle Leg	muscle
24	chr19:42392200-42412800	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr19:42392400-42398200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr19:42392400-42399200	Weak transcription	Fetal Lung	lung
27	chr19:42392400-42399600	Weak transcription	Small Intestine	intestine
28	chr19:42392400-42399800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr19:42392400-42400400	Strong transcription	Stomach Smooth Muscle	stomach
30	chr19:42392400-42401800	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr19:42392400-42407600	Strong transcription	Fetal Intestine Small	intestine
32	chr19:42392400-42410200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr19:42392400-42412400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr19:42392400-42413200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr19:42392600-42396600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr19:42392600-42396800	Strong transcription	GM12878-XiMat	blood
37	chr19:42392600-42397400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr19:42392600-42398200	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr19:42392600-42399800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr19:42392600-42400600	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr19:42392600-42402200	Strong transcription	Adipose Nuclei	Adipose
42	chr19:42392600-42406200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr19:42392600-42407400	Strong transcription	Colonic Mucosa	Colon
44	chr19:42392600-42411800	Strong transcription	Placenta	Placenta
45	chr19:42392600-42413600	Strong transcription	Primary neutrophils fromperipheralblood	blood
46	chr19:42392800-42398800	Genic enhancers	Fetal Thymus	thymus
47	chr19:42392800-42400400	Strong transcription	NHEK	skin
48	chr19:42392800-42400800	Strong transcription	Brain Inferior Temporal Lobe	brain
49	chr19:42392800-42401000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr19:42392800-42402400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood

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