EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS133-23781 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr4:10097000-10099330 
Target genes
Number: 3             
NameEnsembl ID
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MAFFMA0495.3chr4:10097927-10097942CAGCTGACTCAGCAT+6.5
MAFFMA0495.3chr4:10097927-10097942CAGCTGACTCAGCAT-6.64
MAFGMA0659.1chr4:10097924-10097945GTGCAGCTGACTCAGCATTAC+6.15
MAFGMA0659.1chr4:10097924-10097945GTGCAGCTGACTCAGCATTAC-6.24
MAFKMA0496.2chr4:10097925-10097944TGCAGCTGACTCAGCATTA+6.51
MAFKMA0496.2chr4:10097925-10097944TGCAGCTGACTCAGCATTA-6.87
NFE2L1MA0089.2chr4:10097928-10097943AGCTGACTCAGCATT+6.17
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_01734chr4:10091052-10105841Aorta
SE_02758chr4:10093747-10100786Astrocytes
SE_04459chr4:10093617-10105385Brain_Anterior_Caudate
SE_05471chr4:10094965-10100815Brain_Cingulate_Gyrus
SE_08364chr4:10093665-10100812Brain_Inferior_Temporal_Lobe
SE_09623chr4:10091018-10105026CD14
SE_12329chr4:10096638-10099991CD3
SE_14886chr4:10093993-10103243CD4_Memory_Primary_7pool
SE_16236chr4:10097586-10098348CD4_Naive_Primary_7pool
SE_17168chr4:10096964-10099257CD4p_CD225int_CD127p_Tmem
SE_17601chr4:10090784-10114776CD4p_CD25-_CD45RAp_Naive
SE_18041chr4:10091010-10113966CD4p_CD25-_CD45ROp_Memory
SE_18604chr4:10090926-10121361CD4p_CD25-_Il17-_PMAstim_Th
SE_19188chr4:10093472-10113740CD4p_CD25-_Il17p_PMAstim_Th17
SE_21402chr4:10096715-10099370CD8_Memory_7pool
SE_22779chr4:10093720-10112946CD8_primiary
SE_23672chr4:10097154-10098343Colon_Crypt_1
SE_24384chr4:10097197-10097521Colon_Crypt_2
SE_24384chr4:10097753-10098307Colon_Crypt_2
SE_26123chr4:10094261-10099717Duodenum_Smooth_Muscle
SE_27018chr4:10097036-10099939Esophagus
SE_30028chr4:10092826-10099607Fetal_Muscle
SE_32010chr4:10097224-10099371Gastric
SE_37776chr4:10093270-10101196HSMMtube
SE_38833chr4:10093677-10100765HUVEC
SE_39084chr4:10093529-10099686IMR90
SE_41136chr4:10092955-10100158Left_Ventricle
SE_42597chr4:10093130-10099624Lung
SE_45147chr4:10096950-10100917NHLF
SE_48189chr4:10091204-10100769Psoas_Muscle
SE_48835chr4:10091704-10099911Right_Atrium
SE_50444chr4:10094263-10099771Sigmoid_Colon
SE_51167chr4:10091069-10111939Skeletal_Muscle
SE_52707chr4:10094275-10099639Small_Intestine
SE_55072chr4:10096926-10099375Stomach_Smooth_Muscle
SE_55289chr4:10096976-10098234Thymus
SE_66345chr4:10096545-10099342Jurkat
SE_69074chr4:10097155-10098424H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr41009720010098800
Number: 1             
IDChromosomeStartEnd
GH04I010091chr41009329910113947
Enhancer Sequence
TCCCAGGCTT TCCGACCACA TCAGAAGAGC CCACATACGG GAGGAAGCCC AGCGATGCTC 60
AGCCCACCAT GTCCTCAAAG CTGACTGTGG CTGGGCCTCA TGTTAGCACT CACACCTCCT 120
CTCACTTCCC CCAGCCTGCA CGCGCTCCCT TTGTCTTGGG GTTGGTCATG GAGAGCACGA 180
CCGCAGCTTT CCTCTGGGGT CCGGAGGGCT TAAGTGCAGA TACACACCAA AGTGTATCTG 240
CAACTCAGAA GGTATTTGGG GGCAGGTGTG GGGTCCCTGA GCACCCTTCC TGTCCTTCCT 300
ATGCGTGGGC AGTTGAGTCC GCACATGTCT CCTGAGCATG TGGATGGTCA CTGCTGCCTC 360
TCACACCCTC CCTGTGGCTG AGGGTGCAGC ACGCAAGGGT CACTGTCACC CTGTTTCCGG 420
GAGGGCCCAG AGGCATGACT CACCCGAGGG GGGCACAGCC ACCTAGCTCT GTGCCAGGCC 480
ACAGCCCTTT CTATTTCTCC CAGGTCCTCA GGCAGGGCCC ATGGTTGTGG GTTCCACAAA 540
AGACTTCAAG ACACATGGTG GTACCCACCC TGGAGCTGGG CTAGCTGGGC AGACATTTGT 600
ACCCAACACT CCTGGGCCAG GGCAGTGGGG TGAAGTCCTT TCTGAAGTTA GAAAGGACAA 660
CTAAAGAGAA AGAATGTTCT GGACAAGTCC CCAAGCAAGC ACACAGGGGC ACAGCAGCCT 720
GGTGAAGAAG ACAGGCTCCA GCCCACCCCT GGAACAAACT GGTGCCCCTG ACCCTGCTGA 780
GCACCCTGTG CTGGGTTTAA TGCACAGCTG CAGAGTGGAA ATGATCCCTC CCAGGGCAGG 840
CCAAGGAGCC CCCACCCACA GCCGGCTTCT AGCTACCACA GAAGTCTCTG AGCTGCTTCC 900
TCCTGCCCTG GGCTGAGATG GGGTGTGCAG CTGACTCAGC ATTACTCACC CTGCTCTGCA 960
GTGCCTCCAC CCTAGCGAAG AAACATGGCC TGAAGCCACA GCCTTCAATA CAGCTCCCAA 1020
AATAGCCAGG TCTCCACTAC CTACCCATTA GGTGGTAGCC ACAAGAGCAG AGTCTGAGAG 1080
CTGCCGCGTG TTCAGCTGCA TACAGGGAGC CTCCCTATGC TTTCACCTGC CCAGCCAGGC 1140
CCAGCTCAGC CTGCGGTTCC GTGACAAAAT GAAGCCTGTT TCACTACGAA CGGGGCATCC 1200
TTGGAAAGCC CCCTCCTGTA CCCTAAGCCA AGAACAGTCT CTGGAAATTC TGCTCACTTT 1260
GTGGGTCCCG TCCTCGCCCT TTCCAGCTGC ACTGCGCAGG CTATTTATGA TTCATGGCAT 1320
GATGTCACTA AAATGGACAG TGCTCCTCAC TGAGCCACTT TAAGGACATG ATCTCATTAA 1380
TCCTCCATGA GGCAGACAGT GAAACCACTG ACGGTTCCAA GAGGAGTCCC GAGAACTTGG 1440
TCCAATCTGC AAACACAACC TCCTCCAAGG ACATCAACAG TCCCTAAAAT GTGCATTTCC 1500
GGGTCCATTG TTCTTGTCCA TCCTCAGCGC AAGCACAAGC GGGATGGGGA AAGCCAGGGC 1560
AGAGCCGTGG GGTTGTGCTG AGACTGGCTG CTGGGCTCCT CCCCTCACTC CTACAAAGCT 1620
GGGGCAGGAA AATGGGCATC ACAGATGCTC CAGACCTGCC AGGTGGCTCT CCTACTTCAA 1680
ATTCATAGTC AAAACCCTCA GATGCTGCTG GCCCCGGCAC ACCCCCGTCT TGCAGAAGGG 1740
AGAAGTGAGG AGGCTTGGCA AGGCCTGGGT GCCTAAGGCG GGGCGCATGC ACGGCATGGG 1800
CCTCTGAGAT GCTGCCAGCT ACACCCAAAG CCTGCCGCAT TTCTGGCACA TTTCTTCCAC 1860
AAAGTATCTT TCAGTCTTCT AACCGTTTGT CACTTTGCAG GCGCATCACT GCCCTCACTG 1920
TCTCTAGGAG AGACCAATCT GGATGTCCCG CAAGCTCCCT TCCTCTGCCA CTTTGGTGGC 1980
TCAGCTAACA GCAGGCCCTG CAGGCTCCCC TCTCTAATGA GCACCTCCAG CCCCAGATGC 2040
TTGCCTGGTT ACACGGTCAG GGACATTCCT GCCCCAATCC CCGACAGGCA CACATCATCC 2100
TAGGGCAGGG CCCTTCCTTG TGGGAACCAT CCATGCCCAG CTGAGGGCCT GGGGAGGACG 2160
AGTGCTGGGT GGGGGAGCCC TCCCTCTCTC TGCACACCCC TGGGAGCCCA CTTCTGTGTA 2220
TCATGGCATA CGTGGCATGT GCTGTGGTCT CTGCCATCAG CATCTAAACA GGCTCAGCCT 2280
CTGCTAGCCT CATGTACAAA CCACAAATTT CACCCAAAAA GTAAGTTCAC 2330