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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS108-20931
Organism
Homo sapiens
Tissue/cell
K562
Coordinate
chr19:49804330-49804990
Target genes
Number: 53
Name
Ensembl ID
CA11
ENSG00000063180
FUT1
ENSG00000174951
BCAT2
ENSG00000105552
PLEKHA4
ENSG00000105559
PPP1R15A
ENSG00000087074
TULP2
ENSG00000104804
NUCB1
ENSG00000104805
CTD
ENSG00000260366
DHDH
ENSG00000104808
BAX
ENSG00000087088
FTL
ENSG00000087086
GYS1
ENSG00000104812
RUVBL2
ENSG00000183207
NTF4
ENSG00000167744
KCNA7
ENSG00000104848
SNRNP70
ENSG00000104852
AC011450.2
ENSG00000235555
SLC6A16
ENSG00000063127
CD37
ENSG00000104894
AC011450.1
ENSG00000197813
TEAD2
ENSG00000074219
DKKL1
ENSG00000104901
CCDC155
ENSG00000161609
PTH2
ENSG00000142538
SLC17A7
ENSG00000104888
PIH1D1
ENSG00000104872
ALDH16A1
ENSG00000161618
FLT3LG
ENSG00000090554
RPL13A
ENSG00000142541
SNORD33
ENSG00000199631
SNORD35A
ENSG00000200259
RPS11
ENSG00000142534
SNORD35B
ENSG00000200530
FCGRT
ENSG00000104870
RCN3
ENSG00000142552
NOSIP
ENSG00000142546
PRRG2
ENSG00000126460
PRR12
ENSG00000126464
RRAS
ENSG00000126458
SCAF1
ENSG00000126461
BCL2L12
ENSG00000126453
IRF3
ENSG00000126456
PRMT1
ENSG00000126457
C19orf76
ENSG00000224420
CTB
ENSG00000243829
AP2A1
ENSG00000196961
FUZ
ENSG00000010361
MED25
ENSG00000104973
PTOV1
ENSG00000104960
PNKP
ENSG00000039650
AKT1S1
ENSG00000204673
ATF5
ENSG00000169136
NUP62
ENSG00000213024
TF binding sites/motifs
Number: 2
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
CTCF
MA0139.1
chr19:49804697-49804716
CAGCGCCCCCTAGTGGCCT
-
8.17
SREBF2
MA0596.1
chr19:49804446-49804456
ATCACCCCAT
-
6.02
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr19
49804423
49804933
GeneHancer
Number: 1
ID
Chromosome
Start
End
GH19I049301
chr19
49804454
49804937
Enhancer Sequence
AATAAAAATT ACTCTGGAAG AATTGAGAAG TCGGCTTCAG CTGACTTTTA GTGGGAGAAA 60
GAACCCTAGA AAAACCCATA CAGAAAGGGT GGAAAGAACA ATTCCATTTT GCCCACATCA 120
CCCCATCCCC CGAGCCAGCA CTGCTCAGCA TGGAGAGGGA ATTCCCTGGC TCGCATAACC 180
CTCTTTCAGG GATAATGAGA GCAGGCTATA CCACCAGCTT CCCTAGTGTT TTGGGACACT 240
GCCCAACCAG CTTCAGTTTC ACTCCATTCA CATTTCCGTG GGGACTGGCA TTGCCGAGAC 300
TTACGGAGAT AATGGGGAAC CAAGAAGTGG GACAGGCTGT CAGTATCAGC CATGCTGGTG 360
GGAGCCACAG CGCCCCCTAG TGGCCTGCTC AACACGGGTC TCTAGCACAC TTCTGTACTG 420
AGGACCTCAA CAGCACTCCT GGCCACTGTG CAGCTCCCCA CAGTTTTCAC CACCAAGGAC 480
ACCTTGGTGT TACCAATGGC TGATGCCAGC ACCATTTTCT GCAGAGGAAC CAAGCAGCTT 540
TCACAGCTGA GGAAACCAAC TGCCAGCACT GCAGCAGCAA AAGCCCTGTA GTTTTTTCCA 600
CCTTCACAGT CTCCAGGTGC CTGGCCCTCT AATTTCTCCT TCCTCTGTCC CTGAAACCAC 660