EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-20948 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr19:50009780-50010430 
Target genes
Number: 57             
NameEnsembl ID
BCAT2ENSG00000105552
PPP1R15AENSG00000087074
NUCB1ENSG00000104805
DHDHENSG00000104808
BAXENSG00000087088
FTLENSG00000087086
GYS1ENSG00000104812
RUVBL2ENSG00000183207
KCNA7ENSG00000104848
SNRNP70ENSG00000104852
LIN7BENSG00000104863
C19orf73ENSG00000221916
PPFIA3ENSG00000177380
HRCENSG00000130528
TRPM4ENSG00000130529
AC011450.2ENSG00000235555
SLC6A16ENSG00000063127
CD37ENSG00000104894
AC011450.1ENSG00000197813
TEAD2ENSG00000074219
DKKL1ENSG00000104901
CCDC155ENSG00000161609
PTH2ENSG00000142538
CTDENSG00000261949
SLC17A7ENSG00000104888
PIH1D1ENSG00000104872
ALDH16A1ENSG00000161618
FLT3LGENSG00000090554
RPL13AENSG00000142541
SNORD33ENSG00000199631
SNORD35AENSG00000200259
RPS11ENSG00000142534
SNORD35BENSG00000200530
FCGRTENSG00000104870
RCN3ENSG00000142552
NOSIPENSG00000142546
PRRG2ENSG00000126460
PRR12ENSG00000126464
RRASENSG00000126458
SCAF1ENSG00000126461
IRF3ENSG00000126456
PRMT1ENSG00000126457
C19orf76ENSG00000224420
CPT1CENSG00000169169
CTBENSG00000243829
TSKSENSG00000126467
AP2A1ENSG00000196961
FUZENSG00000010361
MED25ENSG00000104973
PTOV1ENSG00000104960
PNKPENSG00000039650
TBC1D17ENSG00000104946
AKT1S1ENSG00000204673
ATF5ENSG00000169136
NUP62ENSG00000213024
IL4I1ENSG00000104951
VRK3ENSG00000105053
TF binding sites/motifs
Number: 12             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr19:50010002-50010021AGGTCAGTAGGGGGCACTA+6.23
ZNF263MA0528.1chr19:50010300-50010321CTTCCCCTTCCCCTCTCCTCT-6.04
ZNF263MA0528.1chr19:50010283-50010304TTCTCCTTCCCCTCCCCCTTC-6.09
ZNF263MA0528.1chr19:50010293-50010314CCTCCCCCTTCCCCTTCCCCT-6.19
ZNF263MA0528.1chr19:50010275-50010296CCTTCCCCTTCTCCTTCCCCT-6.2
ZNF263MA0528.1chr19:50010287-50010308CCTTCCCCTCCCCCTTCCCCT-6.37
ZNF263MA0528.1chr19:50010274-50010295CCCTTCCCCTTCTCCTTCCCC-6.51
ZNF263MA0528.1chr19:50010268-50010289TCCTTTCCCTTCCCCTTCTCC-6.62
ZNF263MA0528.1chr19:50010286-50010307TCCTTCCCCTCCCCCTTCCCC-6.97
ZNF263MA0528.1chr19:50010292-50010313CCCTCCCCCTTCCCCTTCCCC-6.98
ZNF263MA0528.1chr19:50010271-50010292TTTCCCTTCCCCTTCTCCTTC-7.36
ZNF263MA0528.1chr19:50010280-50010301CCCTTCTCCTTCCCCTCCCCC-8.01
Number of super-enhancer constituents: 19             
IDCoordinateTissue/cell
SE_68187chr19:49976788-50037595TC32
SE_68188chr19:49976788-50037595TC32
SE_68189chr19:49976788-50037595TC32
SE_68190chr19:49976788-50037595TC32
SE_68191chr19:49976788-50037595TC32
SE_68192chr19:49976788-50037595TC32
SE_68193chr19:49976788-50037595TC32
SE_68194chr19:49976788-50037595TC32
SE_68464chr19:49990162-50019336TC71
SE_68465chr19:49990162-50019336TC71
SE_68466chr19:49990162-50019336TC71
SE_68467chr19:49990162-50019336TC71
SE_68468chr19:49990162-50019336TC71
SE_68469chr19:49990162-50019336TC71
SE_68470chr19:49990162-50019336TC71
SE_68471chr19:49990162-50019336TC71
SE_68472chr19:49990162-50019336TC71
SE_68473chr19:49990162-50019336TC71
SE_68474chr19:49990162-50019336TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr195001036250010419
chr195001016250010372
chr195000984850010361
Number: 1             
IDChromosomeStartEnd
GH19I049506chr195000979350010480
Enhancer Sequence
TCCGTCTGCC TCGGCCTTCC AAAGTGCTGG GATTATAGGC GTGAGCCACC GTGCCCGGCC 60
TGCAATTGGG GTTTTAATGG CAGAAACCGC AATTACTTTT GCACCACCCT AATATAAAGA 120
CACAATTATT ATCCCCATTT TCCAGATAAA GAACCTTTGG CTGGGAGAGG TGTACCTGGA 180
AGAGTCGTGT TTTGGTTTTG AACTCAGGTG TGATTGCCCC CCAGGTCAGT AGGGGGCACT 240
ATTGTGTAAG GGTGGAGAGG AGGGGCAGCG GTTAGGTGGT TCAGGGTGCA CAGCTCAAAG 300
CTGCCTGGGG CCATTCTAGG CACAGAGGCA GGGGCCAGGG CCGGCTTTAA GGCCAGCTCC 360
TCGTGCAGTC TGAGGAGTGG ATCAGAAGGG ACCAGCACCT GGTGAGTGCT CTACTTGAAC 420
CATCTTGAAA CTGGAACCAA GGGGACCACA TTTTTGTTTT ATGCTGAGTG TGTCCTGCCA 480
TGGGCTTTTC CTTTCCCTTC CCCTTCTCCT TCCCCTCCCC CTTCCCCTTC CCCTCTCCTC 540
TTCTCTTCTC TTCCGTTTTT TGGAGACGGA GTCTTGCTCT GTCGCCCAGG CTGGAGTTCA 600
ATAGCGCAAT CTCGGCTTAC TGCAACCTCC GCCTCCTGGG TTCGAGTGAT 650