EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS133-06069 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr11:67197070-67198540 
Target genes
Number: 41             
NameEnsembl ID
MRPL11ENSG00000174547
CTDENSG00000255517
CCSENSG00000173992
RP11ENSG00000258297
RBM4BENSG00000173914
SPTBN2ENSG00000173898
C11orf80ENSG00000173715
RCE1ENSG00000173653
LRFN4ENSG00000173621
PCENSG00000173599
SYT12ENSG00000173227
RHODENSG00000173156
KDM2AENSG00000173120
ADRBK1ENSG00000173020
ANKRD13DENSG00000172932
SSH3ENSG00000172830
POLD4ENSG00000175482
AP003419.11ENSG00000256514
CLCF1ENSG00000175505
RAD9AENSG00000172613
CARNS1ENSG00000172508
PPP1CAENSG00000172531
RPS6KB2ENSG00000175634
AP003419.16ENSG00000255949
PTPRCAPENSG00000213402
CORO1BENSG00000172725
TMEM134ENSG00000172663
AIPENSG00000110711
PITPNM1ENSG00000110697
CDK2AP2ENSG00000167797
GSTP1ENSG00000084207
NDUFV1ENSG00000167792
DOC2GPENSG00000231793
NUDT8ENSG00000167799
ALDH3B2ENSG00000132746
RPL37P2ENSG00000239559
FAM86C2PENSG00000160172
UNC93B1ENSG00000110057
NDUFS8ENSG00000110717
TCIRG1ENSG00000110719
CHKAENSG00000110721
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12573992chr1167197757hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr11:67197986-67198001TGAACTCCTGACCTC-6.22
Enhancer Sequence
GTCACTCGTT CAGCCAACGA ATACTGTGTG GCTGCCATTC CCAACATGCT GTACCAGGCT 60
TTGGGAAGAC AGCAGGGAAC ACAGTGGAGG AGGATCCCTG ACTTTGGCGT TTGCTGGTTT 120
ATTGTCTGTT GTGATGTGTA TTGTCTTGCA GTAATTCTCA ATGGGGGCAA TTTTGACTCC 180
CAGCAGACAT TTGACAACAG TGTCTGGACA CTATTTTATT TTATTTTTTT TTAAGACGGA 240
GTCTTGCTCT GTCACCCAGG CTGGAGTGCA GTGACGCGAT TTTGGCTCAC TGCCACCTCT 300
GTCTCCCAGG TTCAAGCGAT TCTCGTGCCT TAGACTCCGG AGTAGCTGGG ATTACAGGCG 360
CTTGCCACCA CACCCAGCTA ATTTTTGTAC TTTTTTGTAG AGGTGGGGTT TCGCCTGGCT 420
GGTCTCTAAC TCCTAATCTC AGGTGATCTG CCCGCCTTGG CCTCCAACGT GCTGGGAGCT 480
GGGATTACAG GCATGAGCCA CCGTCCCTAG CTTTTTTTTT TTTTTGGATG GAGTCTTGCT 540
TTGTTCCCCA GACTGGAGTG CAGTAGTGCA CTCTCTGCTC ACTGCAACCT CTGCCTCCCG 600
GGTTCAGGTA ATTCTCTTAC CTCAGCCTCC TGAGTAGTTG GGACTACAGG CTTGTGCCAC 660
CACACCTGGC TAATCTTTGT ATTTCTATTT GTTTACCTAC TTATTTTGAG ACGGAGTCTC 720
ACTCTGTCAC TCAGGCTGGA GTGCAGTGGT GCGATCTCGG CTCACTGGCA ACCTCCACCT 780
CCCAGGGTGA AGTGATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGGATTA CAGGCGTGAA 840
CCACCACTCC TGGCTAATTT TTTTTTTTTG TATTTTTAGT AGAGATGGGT TTTTGTCATG 900
TTGGTCAGGC TGGTCTTGAA CTCCTGACCT CAGGCTATCC GCTCACCTTG GCCTCCCAAA 960
GTGCTGGGAT TACAGCCATG AACCACCGTG CCTGGCCTAG TTTTTGTACT TTTTAGTGGA 1020
GGCAGGGTTT CACCATGTTG GTCAGGCTGG TCTCGAACTC CTGACCTCAG GTGATTCGCC 1080
TGCCTCAACC TCCCAAAGTG CTGGGATTAC AGGTGTGATC CACTGCGCCT GGCATGGACA 1140
CATTTTTGAT TGTCAAGGCA AGAGGGGAGT GTTACTGGCA CCCGGTGGGT GGAGACCAGG 1200
GATGCTGCTG AACATCCCAC GATGCGCAGG GCAGCCTCCC ACAACAAAGA ATGACCTGGT 1260
CCCAGGTGTC AGTAGTGCCG AGGTTGAGAA ACCCTGTGTT AGAGGATAAA CCCATCCCTG 1320
AAAATGATGG TGGCTGACAG CAGCAGAATT ATGGAGAAAT ACAATGCAGT GACAGAGGAT 1380
GCAGCAGTTA ACAAACAGAT GGATGGTCTG AGGAGCTCTG GTTGCCCCCA TTTTTTTTTT 1440
TTTTTTTTTT TTGAGATAGT GTCTCGCTCT 1470