Variant report

Variant	esv1797453
Chromosome Location	chr19:40780963-40786797
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:147)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:147 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr19:40781026-40781347	K562	blood:	n/a	n/a
2	BHLHE40	chr19:40781087-40781345	GM12878	blood:	n/a	n/a
3	BHLHE40	chr19:40786194-40786488	GM12878	blood:	n/a	n/a
4	BRCA1	chr19:40783241-40783245	Hela-S3	cervix:	n/a	n/a
5	CBX3	chr19:40781122-40781516	K562	blood:	n/a	n/a
6	CBX3	chr19:40781831-40782318	K562	blood:	n/a	n/a
7	CHD2	chr19:40786311-40786381	GM12878	blood:	n/a	n/a
8	CHD2	chr19:40780572-40781350	GM12878	blood:	n/a	n/a
9	CTCF	chr19:40785240-40785390	AoAF	blood vessel:	n/a	n/a
10	CTCF	chr19:40785280-40785430	HMF	breast:	n/a	n/a
11	CTCF	chr19:40785160-40785310	HA-sp	spinal cord:	n/a	n/a
12	CTCF	chr19:40785480-40785630	AoAF	blood vessel:	n/a	n/a
13	CTCF	chr19:40785240-40785390	HPAF	blood vessel:	n/a	n/a
14	CTCF	chr19:40785220-40785370	BJ	skin:	n/a	n/a
15	CTCF	chr19:40785280-40785430	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr19:40785200-40785350	AG10803	skin:	n/a	n/a
17	CTCF	chr19:40785220-40785370	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr19:40785320-40785470	HBMEC	blood vessel:	n/a	chr19:40785425-40785434
19	CTCF	chr19:40785240-40785390	AG04449	skin:	n/a	n/a
20	CTCF	chr19:40785280-40785430	HCM	heart:	n/a	n/a
21	CTCF	chr19:40785240-40785390	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr19:40785120-40785270	GM12874	blood:	n/a	n/a
23	CTCF	chr19:40785294-40785359	Fibrobl	skin:	n/a	n/a
24	CTCF	chr19:40785120-40785270	HEK293	kidney:	n/a	n/a
25	CTCF	chr19:40785280-40785430	AG09319	gingival:	n/a	n/a
26	CTCF	chr19:40785260-40785410	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr19:40785320-40785470	NHDF-neo	bronchial:	n/a	chr19:40785425-40785434
28	CTCF	chr19:40785280-40785430	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr19:40785200-40785350	HCFaa	heart:	n/a	n/a
30	CTCF	chr19:40785300-40785450	HPF	lung:	n/a	chr19:40785425-40785434
31	CTCF	chr19:40785280-40785430	AG10803	skin:	n/a	n/a
32	CTCF	chr19:40785240-40785390	AG09319	gingival:	n/a	n/a
33	CTCF	chr19:40785280-40785430	BJ	skin:	n/a	n/a
34	CTCF	chr19:40785220-40785370	HPF	lung:	n/a	n/a
35	CTCF	chr19:40783100-40783250	HEK293	kidney:	n/a	n/a
36	EBF1	chr19:40780943-40781372	GM12878	blood:	n/a	chr19:40781096-40781107
37	EBF1	chr19:40780992-40781390	GM12878	blood:	n/a	chr19:40781096-40781107
38	EBF1	chr19:40780597-40781402	GM12878	blood:	n/a	chr19:40781096-40781107
39	ELF1	chr19:40781058-40781261	K562	blood:	n/a	n/a
40	ELF1	chr19:40785495-40785887	K562	blood:	n/a	chr19:40785706-40785719
41	ELF1	chr19:40780374-40780980	GM12878	blood:	n/a	chr19:40780569-40780582
42	ELF1	chr19:40784800-40786773	GM12878	blood:	n/a	chr19:40785706-40785719
43	ELK1	chr19:40781152-40781202	GM12878	blood:	n/a	n/a
44	EP300	chr19:40786160-40786343	GM12878	blood:	n/a	n/a
45	EP300	chr19:40782922-40782942	K562	blood:	n/a	n/a
46	JUND	chr19:40781343-40781653	K562	blood:	n/a	n/a
47	MAX	chr19:40781058-40781554	K562	blood:	n/a	n/a
48	MAX	chr19:40780434-40781571	K562	blood:	n/a	n/a
49	MAX	chr19:40780701-40781475	K562	blood:	n/a	n/a
50	MAX	chr19:40781028-40781291	GM12878	blood:	n/a	n/a

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:56708147..56710537-chr19:40780894..40783062,2	MCF-7	breast:
2	chr19:40774152..40777118-chr19:40779107..40782198,3	MCF-7	breast:
3	chr19:40776186..40778648-chr19:40782455..40784190,2	MCF-7	breast:
4	chr19:40761210..40764143-chr19:40782426..40783993,2	MCF-7	breast:
5	chr19:40768260..40771807-chr19:40783478..40786593,4	K562	blood:
6	chr19:40778844..40781132-chr19:41035904..41037926,2	K562	blood:
7	chr19:40776409..40778614-chr19:40779445..40781045,2	K562	blood:
8	chr19:40731324..40733318-chr19:40786434..40789035,2	MCF-7	breast:
9	chr19:40776468..40779839-chr19:40784717..40787633,5	MCF-7	breast:
10	chr19:40780031..40782205-chr19:40949064..40951116,2	K562	blood:
11	chr19:40783887..40786272-chr19:41107076..41108731,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC118344.1-2	chr19:40785014-40785131	NONHSAT066360
2	lnc-MAP3K10-1	chr19:40784047-40784243	NONHSAT066362
3	lnc-MAP3K10-1	chr19:40783383-40783496	l_1686_chr19:40779415-40784234_testes
4	lnc-MAP3K10-1	chr19:40783383-40783496	NONHSAT066362
5	lnc-AC118344.1-1	chr19:40780067-40781386	ENSG00000205041.1
6	lnc-MAP3K10-1	chr19:40784047-40784234	l_1686_chr19:40779415-40784234_testes

No data

Variant related genes	Relation type
ENSG00000205041	TF binding region
AKT2	TF binding region
ENSG00000160460	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000105219	chromatin interactions
ENSG00000268366	chromatin interactions
ENSG00000167565	chromatin interactions
ENSG00000090006	chromatin interactions
ENSG00000105221	chromatin interactions

Extended variants
information (count: 234 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:234 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148490745	chr19:40780982-40780983	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
2	rs117029744	chr19:40780983-40780984	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
3	rs79707552	chr19:40781000-40781001	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
4	rs532645470	chr19:40781014-40781015	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
5	rs373990178	chr19:40781043-40781044	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
6	rs201824319	chr19:40781047-40781048	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
7	rs572381232	chr19:40781069-40781070	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
8	rs142610408	chr19:40781088-40781089	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
9	rs371067879	chr19:40781109-40781110	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
10	rs112070825	chr19:40781166-40781167	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
11	rs147626690	chr19:40781167-40781168	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
12	rs191064688	chr19:40781170-40781171	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
13	rs544729861	chr19:40781181-40781182	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
14	rs142011793	chr19:40781205-40781206	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
15	rs533321591	chr19:40781244-40781245	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
16	rs371269969	chr19:40781313-40781314	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
17	rs35080905	chr19:40781316-40781317	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
18	rs560365684	chr19:40781334-40781335	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
19	rs181439226	chr19:40781371-40781372	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
20	rs376848750	chr19:40781387-40781388	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs549154847	chr19:40781396-40781397	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs567553272	chr19:40781400-40781401	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs537522149	chr19:40781409-40781410	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs549819990	chr19:40781450-40781451	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs186175914	chr19:40781474-40781475	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs191036645	chr19:40781484-40781485	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs553807358	chr19:40781512-40781513	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs565977931	chr19:40781550-40781551	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs375170499	chr19:40781566-40781567	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs536591561	chr19:40781606-40781607	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs79885362	chr19:40781643-40781644	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs77995441	chr19:40781685-40781686	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs113854775	chr19:40781690-40781691	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs374718585	chr19:40781698-40781699	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs576217246	chr19:40781745-40781746	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs543278066	chr19:40781775-40781776	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs183404490	chr19:40781797-40781798	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs187527820	chr19:40781798-40781799	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs545380900	chr19:40781808-40781809	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs560152765	chr19:40781813-40781814	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs527962559	chr19:40781816-40781817	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs542941941	chr19:40781850-40781851	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs561268428	chr19:40781851-40781852	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs531899805	chr19:40781858-40781859	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs7260517	chr19:40781943-40781944	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs527769563	chr19:40781984-40781985	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs191217156	chr19:40782001-40782002	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs532155983	chr19:40782002-40782003	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs547408748	chr19:40782118-40782119	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs372205901	chr19:40782122-40782123	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Lung cancer	21569311	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
Anaplastic thyroid cancer	18753363	CNVD
Pleomorphic liposarcoma	18784837	CNVD

Chromatin state (count:513 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40766200-40788600	Weak transcription	HSMMtube	muscle
2	chr19:40769600-40783600	Weak transcription	Fetal Kidney	kidney
3	chr19:40770000-40789600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr19:40770000-40789600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr19:40770200-40789600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr19:40770200-40790200	Weak transcription	Aorta	Aorta
7	chr19:40770400-40784000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr19:40771000-40783600	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr19:40771400-40789400	Weak transcription	HUVEC	blood vessel
10	chr19:40771600-40786000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr19:40776000-40787400	Weak transcription	A549	lung
12	chr19:40776400-40785000	Weak transcription	NHLF	lung
13	chr19:40776600-40783200	Weak transcription	Fetal Intestine Large	intestine
14	chr19:40776600-40783800	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr19:40776600-40785800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr19:40778000-40786400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr19:40778400-40783600	Weak transcription	NHEK	skin
18	chr19:40778600-40784000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr19:40778600-40784400	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr19:40778800-40784200	Weak transcription	HSMM	muscle
21	chr19:40778800-40784200	Weak transcription	Osteobl	bone
22	chr19:40778800-40785200	Weak transcription	HMEC	breast
23	chr19:40778800-40786200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr19:40778800-40787600	Weak transcription	Hela-S3	cervix
25	chr19:40779000-40781600	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr19:40779000-40786800	Weak transcription	Dnd41	blood
27	chr19:40779200-40781400	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr19:40779200-40781400	Enhancers	Fetal Muscle Trunk	muscle
29	chr19:40779200-40781600	Flanking Active TSS	K562	blood
30	chr19:40779200-40782200	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr19:40779400-40781200	Enhancers	Fetal Muscle Leg	muscle
32	chr19:40779400-40781400	Enhancers	Brain Cingulate Gyrus	brain
33	chr19:40779400-40781400	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr19:40779400-40782600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr19:40779400-40789600	Enhancers	Left Ventricle	heart
36	chr19:40779600-40781000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr19:40779600-40781000	Enhancers	Fetal Lung	lung
38	chr19:40779600-40781200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr19:40779600-40781200	Enhancers	Fetal Brain Male	brain
40	chr19:40779600-40781400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr19:40779600-40781400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr19:40779600-40781400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr19:40779600-40781400	Enhancers	Primary T cells fromperipheralblood	blood
44	chr19:40779600-40781400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr19:40779600-40781400	Enhancers	Brain Hippocampus Middle	brain
46	chr19:40779600-40781400	Enhancers	Colonic Mucosa	Colon
47	chr19:40779600-40781400	Genic enhancers	Esophagus	oesophagus
48	chr19:40779600-40781400	Enhancers	Fetal Heart	heart
49	chr19:40779600-40781400	Genic enhancers	Fetal Intestine Small	intestine
50	chr19:40779600-40781400	Enhancers	Pancreas	Pancrea

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