EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS133-11282 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr16:31014220-31015400 
Target genes
Number: 53             
NameEnsembl ID
RP11ENSG00000198064
CD2BP2ENSG00000169217
TBC1D10BENSG00000169221
ZNF48ENSG00000180035
SEPT1ENSG00000180096
ZNF771ENSG00000179965
DCTPP1ENSG00000179958
SEPHS2ENSG00000179918
ZNF768ENSG00000169957
AC002310.12ENSG00000235560
AC002310.11ENSG00000261459
ZNF747ENSG00000169955
AC002310.10ENSG00000260494
AC002310.13ENSG00000260869
ZNF764ENSG00000169951
AC002310.7ENSG00000239791
ZNF688ENSG00000229809
ZNF785ENSG00000197162
AC002310.17ENSG00000261588
ZNF689ENSG00000156853
PRR14ENSG00000156858
FBRSENSG00000156860
SRCAPENSG00000080603
PHKG2ENSG00000156873
RNF40ENSG00000103549
C16orf93ENSG00000196118
ZNF629ENSG00000102870
MIR4519ENSG00000260083
BCL7CENSG00000099385
AC106782.20ENSG00000262721
CTF1ENSG00000150281
FBXL19ENSG00000099364
AC135048.13ENSG00000261487
ORAI3ENSG00000175938
SETD1AENSG00000099381
HSD3B7ENSG00000099377
STX1BENSG00000099365
STX4ENSG00000103496
AC135050.1ENSG00000232748
ZNF668ENSG00000167394
ZNF646ENSG00000167395
PRSS53ENSG00000151006
VKORC1ENSG00000167397
BCKDKENSG00000103507
KAT8ENSG00000103510
PRSS36ENSG00000178226
FUSENSG00000089280
AC106782.18ENSG00000261359
PYCARDENSG00000103490
ARMC5ENSG00000140691
TGFB1I1ENSG00000140682
C16orf58ENSG00000140688
CSDAP1ENSG00000261614
Number: 1             
IDChromosomeStartEnd
GH16I031001chr163101294431015399
Enhancer Sequence
AGAGCTTGCC AGGGTCCCAG CGGAACGCAG ACAGGGCCTA ACAGAAACCA GACAGGCTCA 60
GACTGAACTA GCCGAGGCTC ACACGGATCC CAGACAGATC CCAGACAGCT CAGATTGAAC 120
CTAGACAGGG CCAGATGGGA CCTAGGTGCA GTCCACACAG CCAAAACTCA GGATCAGCAG 180
TGCCCCACAG CCCCAGGAAA AGCCAGCACA GCCTGGGGGG CCTCCAGCTC CACGCTCCTG 240
AGCCACCCCA GCCTCCCTGC TAAGCCCAGC CCAAATGGAA CTCCAGGGAG TCTTCACACA 300
GACGCTGGGC CCACACTGTG TCGGAAAATG TGTTCAGCAC TTGTGTTGAA TTTCCAGACA 360
ATCCCAACCA TCCGCCTGGA AAGGGAGTTT CCTCTGTCTT GGCTCACAGC TGCCCCCAGA 420
AAGTGGGGCG GCACAGGTGG CATAAGTTGG GGACCCTGAG AGGCTCTGGG ATGCTGGGCT 480
CACCTCTGAG GACCCATCGG CCTACCATGA TGCTCTTCAC TTTCTCTGTC CTCAAAATCC 540
AGCTGTGCTA CAAGGCCTCC TTCCCCTAGA GCCAAAAGCC TTCCTCTGCC CTTTCTCTCC 600
CTTCAACCAC TCACTCAGCC ACCAGCCTCA CGCAGGTCAT GCGGCCTCTC CCTGGCCCGG 660
GTGCCTGAGG ACTTTCCTGT TCTCTGTGTC TCTCCCTTCC CCATGCTAAT GTTAGGAAGT 720
CTTTCCTAAA ATCTAATTTC AATCTCTCCT GTTGTTCTTG GAGCCACCTC CCTTAGGTTC 780
ATCTCTGGAG CACCCTGGGC TACCTATTTG TTTGCCCTCA AGACAGGAAG AATGATAGAA 840
GGCCCAAGTG TGGTTTATTT GGTATAATAA ATACAAAGAG AGCTGGGAGC TAATAATCCT 900
CTACCATTTA CAAACACTTT TACATCCATA ATCCGTTTTG ATCCTCAGCA CCACCAGCCC 960
TGAGAGAAAA GCTGCATAAA CATCATCGTC CCCATTTCAC AGATGAGGGA ACAGGAAGCC 1020
AGGGGGGTAA AAGGAGAGTG ACTTGCCCAA GGGCACCCAG GCCACATAGG GCCAGAAAAC 1080
CATGGGCATC CAGCCCCTCA AAGACCGCTG TTAGGCTCCA GACTGGGCTA CCTCCCCCAC 1140
TGACTTTCCG CTCCCAGTTA CTTTCCCTCT CAGTGAGCGC 1180