Variant report

Variant	esv3332013
Chromosome Location	chr19:42400062-42402960
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	CCNT2	chr19:42402192-42402316	K562	blood:	n/a	n/a
2	CTCF	chr19:42400220-42400370	BE2_C	brain:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
3	CTCF	chr19:42400180-42400330	AG09309	skin:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
4	CTCF	chr19:42400160-42400310	HVMF	connective:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
5	CTCF	chr19:42400260-42400410	HFF	foreskin:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
6	CTCF	chr19:42400184-42400349	Fibrobl	skin:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
7	CTCF	chr19:42400240-42400390	GM12872	blood:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
8	CTCF	chr19:42400108-42400431	K562	blood:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
9	CTCF	chr19:42400220-42400370	GM12864	blood:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
10	CTCF	chr19:42400134-42400325	HepG2	liver:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
11	CTCF	chr19:42400100-42400250	AG04450	lung:	n/a	n/a
12	CTCF	chr19:42400220-42400370	HBMEC	blood vessel:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
13	CTCF	chr19:42400160-42400310	HRPEpiC	eye:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
14	CTCF	chr19:42400160-42400310	A549	lung:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
15	CTCF	chr19:42400180-42400330	WERI-Rb-1	eye:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
16	CTCF	chr19:42399572-42400749	A549	lung:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
17	CTCF	chr19:42400200-42400350	HMF	breast:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
18	CTCF	chr19:42400182-42400371	Hela-S3	cervix:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
19	CTCF	chr19:42400180-42400330	K562	blood:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
20	CTCF	chr19:42400151-42400370	A549	lung:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
21	CTCF	chr19:42400240-42400390	WERI-Rb-1	eye:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
22	CTCF	chr19:42400230-42400352	ProgFib	skin:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
23	CTCF	chr19:42400204-42400339	SK-N-SH_RA	brain:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
24	CTCF	chr19:42400122-42400428	GM12891	blood:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
25	CTCF	chr19:42400180-42400330	SK-N-SH_RA	brain:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
26	CTCF	chr19:42400200-42400470	GM12869	blood:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
27	CTCF	chr19:42400120-42400270	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr19:42400194-42400379	HepG2	liver:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
29	CTCF	chr19:42400140-42400290	HRE	kidney:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
30	CTCF	chr19:42400180-42400330	GM12866	blood:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
31	CTCF	chr19:42400180-42400330	GM12864	blood:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
32	CTCF	chr19:42400160-42400310	NB4	blood:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
33	CTCF	chr19:42400220-42400370	GM12873	blood:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
34	CTCF	chr19:42400240-42400390	HRE	kidney:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
35	CTCF	chr19:42400180-42400330	SAEC	small airway:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
36	CTCF	chr19:42400160-42400310	Caco-2	colon:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
37	CTCF	chr19:42400200-42400350	NHEK	skin:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
38	CTCF	chr19:42399960-42400110	BE2_C	brain:	n/a	n/a
39	CTCF	chr19:42400180-42400330	Caco-2	colon:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
40	CTCF	chr19:42400158-42400436	GM12878	blood:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
41	CTCF	chr19:42400152-42400402	MCF-7	breast:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
42	CTCF	chr19:42400140-42400290	HCFaa	heart:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
43	CTCF	chr19:42400154-42400394	Gliobla	brain:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
44	CTCF	chr19:42400161-42400409	H1-hESC	embryonic stem cell:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
45	CTCF	chr19:42400231-42400332	GM10248	blood:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
46	CTCF	chr19:42400180-42400330	HUVEC	blood vessel:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
47	CTCF	chr19:42400200-42400350	GM12865	blood:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
48	CTCF	chr19:42400117-42400430	MCF-7	breast:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
49	CTCF	chr19:42400200-42400350	K562	blood:	n/a	chr19:42400263-42400281 chr19:42400269-42400278
50	CTCF	chr19:42400153-42400391	A549	lung:	n/a	chr19:42400263-42400281 chr19:42400269-42400278

No.	Distal block	Cell Line	Cell type
1	chr19:42388132..42389933-chr19:42401964..42404218,2	K562	blood:
2	chr19:42387549..42389204-chr19:42401111..42402879,2	MCF-7	breast:
3	chr19:42399993..42402789-chr19:42426992..42429764,2	MCF-7	breast:
4	chr19:42400938..42403112-chr19:42412847..42414847,2	MCF-7	breast:
5	chr19:42400726..42402812-chr19:42407325..42408926,2	K562	blood:
6	chr19:42385849..42388501-chr19:42399623..42401678,2	K562	blood:
7	chr19:42398480..42400174-chr19:42432062..42434996,2	K562	blood:
8	chr19:42397636..42399907-chr19:42401318..42404591,3	K562	blood:
9	chr19:42398848..42401100-chr19:42409902..42411983,2	MCF-7	breast:
10	chr19:42399554..42401550-chr19:42461897..42463730,2	MCF-7	breast:
11	chr19:42400409..42404033-chr19:42410840..42416491,6	K562	blood:
12	chr19:42399244..42402499-chr19:42406088..42408738,6	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LYPD4-2	chr19:42400853-42400876	NONHSAT066499
2	lnc-LYPD4-2	chr19:42400449-42400876	NONHSAT066498
3	lnc-LYPD4-2	chr19:42400972-42402807	NONHSAT066497
4	lnc-LYPD4-2	chr19:42401027-42401182	NONHSAT066498
5	lnc-LYPD4-2	chr19:42400176-42400914	NONHSAT066497
6	lnc-LYPD4-2	chr19:42400991-42402843	NONHSAT066499

Variant related genes	Relation type
ARHGEF1	TF binding region
ENSG00000076928	chromatin interactions
ENSG00000105404	chromatin interactions
ENSG00000268041	chromatin interactions

Extended variants
information (count: 141 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:141 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534516347	chr19:42400097-42400098	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs111653018	chr19:42400107-42400108	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs574317412	chr19:42400168-42400169	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs113612675	chr19:42400258-42400259	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs140922185	chr19:42400307-42400308	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs577948254	chr19:42400313-42400314	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs374399568	chr19:42400314-42400315	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs545340465	chr19:42400332-42400333	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs544320343	chr19:42400333-42400334	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs373980194	chr19:42400348-42400349	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs189510461	chr19:42400350-42400351	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs527547130	chr19:42400379-42400380	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs542546878	chr19:42400386-42400387	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs200462152	chr19:42400402-42400403	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs201715322	chr19:42400404-42400405	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs11368847	chr19:42400406-42400407	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs397960735	chr19:42400408-42400409	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs557906235	chr19:42400409-42400410	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs549598488	chr19:42400410-42400411	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs199618317	chr19:42400415-42400416	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs370019084	chr19:42400427-42400428	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs201322553	chr19:42400445-42400446	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs113064588	chr19:42400457-42400458	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs200492200	chr19:42400458-42400459	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs547343524	chr19:42400469-42400470	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs370209568	chr19:42400486-42400487	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs138912380	chr19:42400504-42400505	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs534481909	chr19:42400509-42400510	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
29	rs373879693	chr19:42400516-42400517	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs199751095	chr19:42400528-42400529	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs199929341	chr19:42400535-42400536	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
32	rs370619761	chr19:42400545-42400546	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
33	rs375093075	chr19:42400560-42400561	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
34	rs143491843	chr19:42400579-42400580	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
35	rs577777929	chr19:42400593-42400594	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
36	rs146744506	chr19:42400601-42400602	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
37	rs572134419	chr19:42400625-42400626	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
38	rs542508183	chr19:42400654-42400655	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
39	rs181061311	chr19:42400692-42400693	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
40	rs561796835	chr19:42400706-42400707	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
41	rs531514125	chr19:42400714-42400715	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
42	rs79911897	chr19:42400729-42400730	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
43	rs564957315	chr19:42400752-42400753	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs532201606	chr19:42400769-42400770	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs79725225	chr19:42400789-42400790	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
46	rs147215129	chr19:42400861-42400862	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
47	rs200018784	chr19:42400864-42400865	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs587756094	chr19:42400874-42400875	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs116682533	chr19:42400883-42400884	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
50	rs587684956	chr19:42400884-42400885	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Breast cancer	22522925	CNVD

Chromatin state (count:246 , 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	chr19:42389400-42402000	Weak transcription	Psoas Muscle	Psoas
4	chr19:42389400-42406000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr19:42389400-42411400	Weak transcription	Fetal Brain Male	brain
6	chr19:42389800-42409000	Strong transcription	Fetal Stomach	stomach
7	chr19:42390800-42411200	Weak transcription	Hela-S3	cervix
8	chr19:42391400-42407400	Weak transcription	K562	blood
9	chr19:42391600-42404600	Weak transcription	HSMM	muscle
10	chr19:42392000-42404000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr19:42392000-42412600	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr19:42392000-42412600	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr19:42392000-42412600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr19:42392200-42400800	Strong transcription	Skeletal Muscle Male	skeletal muscle
15	chr19:42392200-42401400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr19:42392200-42407600	Strong transcription	Sigmoid Colon	Sigmoid Colon
17	chr19:42392200-42408400	Strong transcription	Liver	Liver
18	chr19:42392200-42412400	Strong transcription	Fetal Muscle Leg	muscle
19	chr19:42392200-42412800	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr19:42392400-42400400	Strong transcription	Stomach Smooth Muscle	stomach
21	chr19:42392400-42401800	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr19:42392400-42407600	Strong transcription	Fetal Intestine Small	intestine
23	chr19:42392400-42410200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr19:42392400-42412400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr19:42392400-42413200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr19:42392600-42400600	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr19:42392600-42402200	Strong transcription	Adipose Nuclei	Adipose
28	chr19:42392600-42406200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr19:42392600-42407400	Strong transcription	Colonic Mucosa	Colon
30	chr19:42392600-42411800	Strong transcription	Placenta	Placenta
31	chr19:42392600-42413600	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr19:42392800-42400400	Strong transcription	NHEK	skin
33	chr19:42392800-42400800	Strong transcription	Brain Inferior Temporal Lobe	brain
34	chr19:42392800-42401000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr19:42392800-42402400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr19:42392800-42407800	Strong transcription	Fetal Intestine Large	intestine
37	chr19:42393000-42403600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
38	chr19:42393400-42400800	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr19:42393400-42400800	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
40	chr19:42393400-42404600	Genic enhancers	Primary T helper cells PMA-I stimulated	--
41	chr19:42393400-42413600	Strong transcription	Thymus	Thymus
42	chr19:42393800-42401800	Weak transcription	NH-A	brain
43	chr19:42393800-42402200	Genic enhancers	Primary T cells from cord blood	blood
44	chr19:42393800-42404400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr19:42393800-42413000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr19:42394000-42403400	Genic enhancers	Primary T cells fromperipheralblood	blood
47	chr19:42394000-42413000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr19:42394200-42401000	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr19:42394800-42405000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr19:42395200-42400600	Strong transcription	Rectal Mucosa Donor 31	rectum

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