EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-18984 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr19:844040-845000 
Target genes
Number: 44             
NameEnsembl ID
WDR18ENSG00000065268
FGF22ENSG00000070388
RNF126ENSG00000070423
FSTL3ENSG00000070404
PRSS57ENSG00000185198
PALMENSG00000099864
C19orf21ENSG00000099812
AC004449.6ENSG00000261204
AC112708.1ENSG00000213726
RN5S462ENSG00000252539
ARID3AENSG00000116017
KISS1RENSG00000116014
R3HDM4ENSG00000198858
MED16ENSG00000175221
PTBP1ENSG00000011304
LPPR3ENSG00000129951
CFDENSG00000197766
ELANEENSG00000197561
PRTN3ENSG00000196415
AZU1ENSG00000172232
GZMMENSG00000197540
MIER2ENSG00000105556
TPGS1ENSG00000141933
CDC34ENSG00000099804
BSGENSG00000172270
GRIN3BENSG00000116032
C19orf6ENSG00000182087
CNN2ENSG00000064666
ABCA7ENSG00000064687
HMHA1ENSG00000180448
POLR2EENSG00000099817
GPX4ENSG00000167468
SBNO2ENSG00000064932
STK11ENSG00000118046
C19orf26ENSG00000099625
ATP5DENSG00000099624
MIDNENSG00000167470
CIRBPENSG00000099622
C19orf24ENSG00000228300
NDUFS7ENSG00000115286
GAMTENSG00000130005
DAZAP1ENSG00000071626
RPS15ENSG00000115268
REEP6ENSG00000115255
Number: 1             
IDChromosomeStartEnd
GH19I000843chr19843108844883
Enhancer Sequence
GGGCAGGGCC GCGAGGGCTC GGAGGGGCAC GGCCAGAGGG CTCCGGGACC CCCATTCCTG 60
CAGCCAGCAT TCATTGAGCA CCCACTGTAT ACCGGGCCAC GACCGAGGCC GCTGCAGCCT 120
GGGTCCAGTG GCACTGGCCG GGGGAGACCG CTCCTTGGAC ACCAGGCCAC TCCTCCTCCC 180
CGCCTCTCCC CCGCCCGCGC CTCTCCCCCG CCCGCGCCTC TCCCCTGCGC GCCTCTCCCC 240
CGCCCGCGCC TCTCCCCCGC CCGCGCCTCT CCCCCGCCCG CGCCTCTCCC TTGCCCGCCC 300
CTCTCCCCTG CCCGCGCCTC TCCCCTGCAT GCCTCTCCCT TGCCCGCCCC TCTCCCCTGC 360
CCGCGCCTCT CCCCTGCGCG CCTCTCCCCT GCCCGCGCCT CTCCCCCGGC CGCTCCTCTC 420
CCCCGCCCGC GCCTCTCCCC CGCCCGCGCC TCTCCCCTGC GCGCCTCTCC CCTGCCTGCC 480
CCTCTCCCCT GCCTGCGCCT CCGCCCGGTG TGCTGTTCCC CCAGAAAGCC AGGTGCCCTC 540
GCCTCCTCCG GCGCCTCCCC TGACCTCACT GGAAGTGGCG AGGACAGCCA CAGCCCTCCC 600
CGATTCACTG TTCTCCACTG AACCGCGTGC TCCTCTCATT CATGGGGCCC TCCTAGCCTC 660
CTCCCACCCA GAAAGATCAG CTCCCCAGGG CAGAGGATTT TTGTCTGTGT TGTTCGTTAT 720
TGGACTCATG TGGCTTAGAA CGGGACTGGG CATACAGGTG GTGCTCAGTA AGTGCTTGGG 780
GTTGGGCACT GTGGCTCACG CCTGTACTCC CAGTACTTTG GGAGGCTGGG ATGGGAGGAT 840
CACTTGAGGC CAGGAGTTTG GGAGCAGCCT GACCAACCTA GTGAGACCCC ATCTCTATAA 900
AAGACATTTT TTTTTTTTTT TTTTTTAGAC AGAGTCTCAC TCAGTCATCC AGGCTGGAGT 960