EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS076-27404 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr19:678790-680270 
Target genes
Number: 49             
NameEnsembl ID
WDR18ENSG00000065268
HCN2ENSG00000099822
FGF22ENSG00000070388
RNF126ENSG00000070423
FSTL3ENSG00000070404
PRSS57ENSG00000185198
PALMENSG00000099864
AC004449.6ENSG00000261204
AC112708.1ENSG00000213726
ARID3AENSG00000116017
KISS1RENSG00000116014
R3HDM4ENSG00000198858
MED16ENSG00000175221
PTBP1ENSG00000011304
LPPR3ENSG00000129951
CFDENSG00000197766
ELANEENSG00000197561
PRTN3ENSG00000196415
AZU1ENSG00000172232
GZMMENSG00000197540
PPAP2CENSG00000141934
MIER2ENSG00000105556
C2CD4CENSG00000183186
SHC2ENSG00000129946
ODF3L2ENSG00000181781
MADCAM1ENSG00000099866
TPGS1ENSG00000141933
CDC34ENSG00000099804
BSGENSG00000172270
GRIN3BENSG00000116032
C19orf6ENSG00000182087
CNN2ENSG00000064666
ABCA7ENSG00000064687
HMHA1ENSG00000180448
POLR2EENSG00000099817
GPX4ENSG00000167468
SBNO2ENSG00000064932
STK11ENSG00000118046
ATP5DENSG00000099624
MIDNENSG00000167470
CIRBPENSG00000099622
C19orf24ENSG00000228300
MUM1ENSG00000160953
EFNA2ENSG00000099617
AC005330.1ENSG00000240846
AC005329.7ENSG00000248015
C19orf25ENSG00000119559
ADAMTSL5ENSG00000185761
MEX3DENSG00000181588
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
STAT3MA0144.2chr19:679899-679910CTTCCCAGAAG-6.14
ZBTB18MA0698.1chr19:679259-679272TTTCCAGATGTGC+6
Number of super-enhancer constituents: 9             
IDCoordinateTissue/cell
SE_01056chr19:674694-682124Adrenal_Gland
SE_27051chr19:678848-681642Esophagus
SE_34552chr19:678601-682145HCT-116
SE_37659chr19:674743-681671HSMMtube
SE_43189chr19:674801-681203Lung
SE_50861chr19:679139-681710Sigmoid_Colon
SE_53880chr19:679325-681855Spleen
SE_57506chr19:679618-680539VACO_503
SE_65940chr19:676609-680305Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr19678997679265
Enhancer Sequence
GTGAGCCACC ATGCCTGGCC TGTTGGGGCA CATCTTGAAG GAGGTGGGCA TTAGAGCTGG 60
GGTGTTGGGG GATGTCTAGG AGTTTGCCAG ATGGGGCCGG TATGGGAGAG TGGATCAGGA 120
GAGAACATGG CTTGAGGTTA GGTCCTGGTG GGTGGGGTCA GGCAGAGGAG CCAAGGGGAG 180
GCTGAAGCTG AGGGCTGCAG ACCCGAAGGC CAGGCTGAGG AACTCTGCTG GCCTCTGAGA 240
TGTGATTAAT CCCAGATCAG CCTGGCTGGG TGGTCCTGAA CTCACTGCCA CATACCCCTG 300
CTCCCTCCAG ACCCCCCTCT GGCTTCTGGG AGAAGGACAG TCTTCAAAAA GTGCCTGGCC 360
TGGGCATGAG ACGGCCCAGG ACCCCCCACC CCCAACCTCA TCTGGCCCTG GGGACGGAAC 420
TCAGGCCCCC TTCCGTTCTC GCTCGCATAA AAGCCACCCT GGCCGAGCAT TTCCAGATGT 480
GCCTGTGAGC CGCTGTGCCG GGGCCGCCCA GGTGCGGCCC ACATGCCCTG CAAGGGCTGC 540
GTGGCGGGCG CTGGCCATCC CCTAAGGAGT GCCGCACTGC CTTGGAAGTG GGGCTCCCTC 600
GTCAGCCCCA CTTTACACAC AGAGAAACTG AGGCTGGCAC ATAAACTCAA CAGCTGTGTT 660
CAGAGGCCCT ACCAGACCCC CAGATAACAG AAAGGGGGTT GGTCATCTGG GTCCTGGCTG 720
CAGCTTTCAA ACTGAGGTGC TTGGGCCCCT GCACTCATAG CTGCGACCCG GCCTCAGTTT 780
CCCCATCTGT AAAATGATGA CTTGGGAAGA TGCGATAAGC CTAGGAGGCG ATGAGCATTC 840
ACATTGAAAG CGGGGGCGGG GACCCCAGAG AGAGCTTCCC TAGCAGGACC TCAATATCCC 900
TGTCTGAGCA GCGGGGCTGC GGGGCAGCTC CTGGTTCAGA GGCCTAGGGC TGTGGGGGGC 960
CCCCTCCCCT GGAATCGCTC CCCAGGCCAG GAGGGCCGTC CAGCGCCCCG CCCTCCCCGA 1020
CGCCTCCTGG GGGAAGGTCC TGGCAGCCCC AGACTCGCGC CTGGCAAGGG CGGAACACCC 1080
CAGGCTGACG CAGCTGGGGC CCCTCCGGCC TTCCCAGAAG AGCGCGTGCA TCGGGAGCAG 1140
ACGTCAGCCA GCTGCAAGGA GGAGCGGCCC GGGGCTGCGT AGCTCCGCTG GACCCCGATT 1200
CCGGGCAGAG ACCCCCCCCC GCCCCGGCCC GCGCGCACCG AGCCCAGCCC CCGCCCCCCA 1260
GCGCAGGCGC AGCGCGGACC TCGGCCCCAC CGGTCCCGCG CCCGGACCCT GAGCCCTGCC 1320
CCTGGGAACC CGAGGGCCCC GACTCCGACT GACCCTGACC TGGGACGGCG CCCCCGCCTC 1380
CGCCCTGCAG AAGGGGCGCA GGGAGGGGCC CCGAGGCCTT CGCGCGGCCC CACGCCCGGG 1440
ACCCTCCCGC GCCCGGCCCC ACGCGCGTGT CCTCTGTCCG 1480