EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS133-23783 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr4:10107700-10109750 
Target genes
Number: 4             
NameEnsembl ID
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SNAI2MA0745.2chr4:10109213-10109223AACAGGTGCA+6.02
ZNF263MA0528.1chr4:10108588-10108609CTCCCCCCAGCCTCCTCCCCC-6.28
ZNF263MA0528.1chr4:10108585-10108606CCTCTCCCCCCAGCCTCCTCC-6.76
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_01734chr4:10107077-10115538Aorta
SE_02758chr4:10107837-10109726Astrocytes
SE_04459chr4:10105408-10112471Brain_Anterior_Caudate
SE_05471chr4:10107753-10111919Brain_Cingulate_Gyrus
SE_08364chr4:10105438-10111735Brain_Inferior_Temporal_Lobe
SE_09623chr4:10105351-10111775CD14
SE_12329chr4:10106211-10109483CD3
SE_14886chr4:10105405-10112347CD4_Memory_Primary_7pool
SE_16236chr4:10107851-10108756CD4_Naive_Primary_7pool
SE_17168chr4:10107218-10109553CD4p_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_21402chr4:10105556-10109263CD8_Memory_7pool
SE_22779chr4:10093720-10112946CD8_primiary
SE_23672chr4:10107865-10108914Colon_Crypt_1
SE_26123chr4:10104074-10111938Duodenum_Smooth_Muscle
SE_27018chr4:10105236-10112495Esophagus
SE_30028chr4:10107770-10109367Fetal_Muscle
SE_32010chr4:10107854-10111601Gastric
SE_37776chr4:10105574-10112955HSMMtube
SE_38833chr4:10106987-10111433HUVEC
SE_39084chr4:10107151-10108374IMR90
SE_39084chr4:10108404-10111446IMR90
SE_41136chr4:10105238-10111825Left_Ventricle
SE_42597chr4:10105406-10113504Lung
SE_45147chr4:10107819-10109685NHLF
SE_46972chr4:10107906-10108298Ovary
SE_46972chr4:10108380-10111760Ovary
SE_48189chr4:10100794-10113550Psoas_Muscle
SE_48835chr4:10100802-10111531Right_Atrium
SE_50444chr4:10105296-10113383Sigmoid_Colon
SE_51167chr4:10091069-10111939Skeletal_Muscle
SE_52707chr4:10105393-10112888Small_Intestine
SE_55072chr4:10106115-10109264Stomach_Smooth_Muscle
SE_55289chr4:10107856-10108311Thymus
SE_69074chr4:10107907-10110233H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr41010780010109200
chr41010791710109108
Number: 1             
IDChromosomeStartEnd
GH04I010091chr41009329910113947
Enhancer Sequence
CAGATAAGCA GCTGCTGGGG GTGAGGGTGG AAGGGGTGGC GGGGGCGGGG GGCACCCTCC 60
GGAGTGACAG GAATGTTCTG TCATGACAGG GGTGGTGCTT ATGGGACTAT ATAGGTCATC 120
TGTCAAGATC CAAGCCACAC ACTGAATACA GACAAATTCT ACTGTATCTA AAGTACACCT 180
CAATAAAACT AAGATGCTGG CTATTTATTA AATGTCTGCC CAATCCAACC CTCTCCCACT 240
CCAATTAGTC CTTCATATTC TGACACTGAC ACATCCCTAC CCAAAGCACC TGGCAAGAAA 300
ATGATCCACT TAACAGGCAG CCCCTCCAAG ACCCTGTTCG GTGTACACTC ACAGCTGACT 360
GGGGATGGGG GAGGTCTCAC GCTCACATAC AGGGGCACCT GCCCATCCCG CCAGACAGAT 420
GGCCTCGTGG GCTCTCCCAG CCTGGACGAC CTCCTCCCCA GGCCGTGCTG CCGTAGAAAG 480
GGTGGGGCTC CCATGGGCCT TCCGCTGGGG AGGGCATCCA GAGATGGAAG ATGCCTGGGC 540
AGGGGCATGA GAGGAAGTTC TGCCCCTAAA AATTCCTTCC CCTAAATGGT CAGGGCTGTG 600
TGTAAAAACC CCAAAGGGCA ACAGAATCCT GCCAGCTGAT GAATCACTCA CTCTCGTTTG 660
TATTCTAAAT ACAACTGGGT CAGCGGTGGG GGCTGAGATA CTCCAAACTG CAGATAATGA 720
CTTACATCTG AGTCAGAGCA GCCTCCTCCC CAGCTCCTCA GCTCGCAGAG GGAGGCTGCT 780
TACTACACCC AGAAAGATAC CTCACACCCC CACGTGTCAC TCGGCCTGTG AGGCTCTGTC 840
CCCATCAGCT GGGTCGAGAT GGCACCTTGA CACCCTCAGT GTGCCCCTCT CCCCCCAGCC 900
TCCTCCCCCT CCTTCCATCT TGGGGAAGAA GAATGAGATT GGGGGTTGAG AAGCTTATTT 960
GGGGAAAAAC TCTGGAATGG GGAAAACGAG ACAGGGAGGG CAGGAAGCCA ATTCCAGGAG 1020
CCCCAGTGCT ACTGTAGGCA AAAGTTCTGT CTCCCCATCT CCCTGGGGGC CTGGGGGAGA 1080
CCACCATGAG CAGCCTTGGA GTTGCCCACT CAGGGACACC CCTCCTCCCA GGCTTTCTTC 1140
TCATGCTGCT GCAGGCTGGG CCAGCTCTGG CAGTGGGAGG CTGCCGTTCA GTCCTCACCA 1200
CAGGCCTGCC CAGTTTTCCT TGCCAACTCC CAACCCATCT TCTCTTTTAC CTCCACCATT 1260
TTCAATGCAG TCCTCCTGTT CTTCCTGGGA AGAGCGATAA CTGCTTTGGA ATGCATCTCC 1320
ACCCTCCACC AAGCCGGTAG TCTTCAAATC CCGACCCTGA TTACCTCACG GTCCGGCTTG 1380
CAACCCACCC TTCCTGAGCT CCCTCCAGGC TTCAGCCCAC TCGTCGCTAC CCTGCTGCCG 1440
CCCTGACGTT GCCAGCCACT CCTTGGGCTG ACTACCCCAA CCCATGGCCC CTCACCCCAA 1500
CCCTTGAGGA TAGAACAGGT GCAGCCCCTC TACCTTGCTG GCCCCAGACC CCTTCCCCAG 1560
TGGCCTCCAC ACCTGGGGGC TAGGGCCTGT GAGGGCCAGA GCTGGGGCTG GGATAAGACC 1620
TCGAGACAAG CCCCAGAATT CTGCCACCAC CCCTGGAGGA GTCCGGGGGC CTCTGAGGAC 1680
ATGAAGGACA CCAGCCAGCA ATCAAGGAGT CACACACGCG AGCAGACCCA GGACCCACGG 1740
ACTTCGGCAA GTGACAGCAT GTAACAGCAC CCAGCCCTGC CAACACAGGG CCTGGTTCAA 1800
GGCCCAGTGG TGCCCATTTG AAGCAGAAGC TTTGGACTTG ACCCGGGAGG CCATTCTACT 1860
CTGTCACACT ATGCTCAGGT CCCACCAGCC CCCACCTCCC ACCTGTGCAC TGAGGCATCC 1920
TGCCCAGGAA TAGCTGGTCT TTTTCTGAGA ATCCTGTTGA ATGGCAAACC TAAACATACT 1980
CCCCCCCGGC ACCTGTACAA TGTCTGTGCC GCCTTTGAGA CTCGCTATAA TACACAGGTC 2040
ATGCAAACAA 2050