EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS094-29373 
Organism
Homo sapiens 
Tissue/cell
hMADS-3 
Coordinate
chr4:10096970-10099330 
Target genes
Number: 6             
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: 2             
ChromosomeStartEnd
chr41009698810099002
chr41009720010098800
Number: 1             
IDChromosomeStartEnd
GH04I010091chr41009329910113947
Enhancer Sequence
AGGCTCAATT AATTCCTGAG AACTTCCACA TCCCAGGCTT TCCGACCACA TCAGAAGAGC 60
CCACATACGG GAGGAAGCCC AGCGATGCTC AGCCCACCAT GTCCTCAAAG CTGACTGTGG 120
CTGGGCCTCA TGTTAGCACT CACACCTCCT CTCACTTCCC CCAGCCTGCA CGCGCTCCCT 180
TTGTCTTGGG GTTGGTCATG GAGAGCACGA CCGCAGCTTT CCTCTGGGGT CCGGAGGGCT 240
TAAGTGCAGA TACACACCAA AGTGTATCTG CAACTCAGAA GGTATTTGGG GGCAGGTGTG 300
GGGTCCCTGA GCACCCTTCC TGTCCTTCCT ATGCGTGGGC AGTTGAGTCC GCACATGTCT 360
CCTGAGCATG TGGATGGTCA CTGCTGCCTC TCACACCCTC CCTGTGGCTG AGGGTGCAGC 420
ACGCAAGGGT CACTGTCACC CTGTTTCCGG GAGGGCCCAG AGGCATGACT CACCCGAGGG 480
GGGCACAGCC ACCTAGCTCT GTGCCAGGCC ACAGCCCTTT CTATTTCTCC CAGGTCCTCA 540
GGCAGGGCCC ATGGTTGTGG GTTCCACAAA AGACTTCAAG ACACATGGTG GTACCCACCC 600
TGGAGCTGGG CTAGCTGGGC AGACATTTGT ACCCAACACT CCTGGGCCAG GGCAGTGGGG 660
TGAAGTCCTT TCTGAAGTTA GAAAGGACAA CTAAAGAGAA AGAATGTTCT GGACAAGTCC 720
CCAAGCAAGC ACACAGGGGC ACAGCAGCCT GGTGAAGAAG ACAGGCTCCA GCCCACCCCT 780
GGAACAAACT GGTGCCCCTG ACCCTGCTGA GCACCCTGTG CTGGGTTTAA TGCACAGCTG 840
CAGAGTGGAA ATGATCCCTC CCAGGGCAGG CCAAGGAGCC CCCACCCACA GCCGGCTTCT 900
AGCTACCACA GAAGTCTCTG AGCTGCTTCC TCCTGCCCTG GGCTGAGATG GGGTGTGCAG 960
CTGACTCAGC ATTACTCACC CTGCTCTGCA GTGCCTCCAC CCTAGCGAAG AAACATGGCC 1020
TGAAGCCACA GCCTTCAATA CAGCTCCCAA AATAGCCAGG TCTCCACTAC CTACCCATTA 1080
GGTGGTAGCC ACAAGAGCAG AGTCTGAGAG CTGCCGCGTG TTCAGCTGCA TACAGGGAGC 1140
CTCCCTATGC TTTCACCTGC CCAGCCAGGC CCAGCTCAGC CTGCGGTTCC GTGACAAAAT 1200
GAAGCCTGTT TCACTACGAA CGGGGCATCC TTGGAAAGCC CCCTCCTGTA CCCTAAGCCA 1260
AGAACAGTCT CTGGAAATTC TGCTCACTTT GTGGGTCCCG TCCTCGCCCT TTCCAGCTGC 1320
ACTGCGCAGG CTATTTATGA TTCATGGCAT GATGTCACTA AAATGGACAG TGCTCCTCAC 1380
TGAGCCACTT TAAGGACATG ATCTCATTAA TCCTCCATGA GGCAGACAGT GAAACCACTG 1440
ACGGTTCCAA GAGGAGTCCC GAGAACTTGG TCCAATCTGC AAACACAACC TCCTCCAAGG 1500
ACATCAACAG TCCCTAAAAT GTGCATTTCC GGGTCCATTG TTCTTGTCCA TCCTCAGCGC 1560
AAGCACAAGC GGGATGGGGA AAGCCAGGGC AGAGCCGTGG GGTTGTGCTG AGACTGGCTG 1620
CTGGGCTCCT CCCCTCACTC CTACAAAGCT GGGGCAGGAA AATGGGCATC ACAGATGCTC 1680
CAGACCTGCC AGGTGGCTCT CCTACTTCAA ATTCATAGTC AAAACCCTCA GATGCTGCTG 1740
GCCCCGGCAC ACCCCCGTCT TGCAGAAGGG AGAAGTGAGG AGGCTTGGCA AGGCCTGGGT 1800
GCCTAAGGCG GGGCGCATGC ACGGCATGGG CCTCTGAGAT GCTGCCAGCT ACACCCAAAG 1860
CCTGCCGCAT TTCTGGCACA TTTCTTCCAC AAAGTATCTT TCAGTCTTCT AACCGTTTGT 1920
CACTTTGCAG GCGCATCACT GCCCTCACTG TCTCTAGGAG AGACCAATCT GGATGTCCCG 1980
CAAGCTCCCT TCCTCTGCCA CTTTGGTGGC TCAGCTAACA GCAGGCCCTG CAGGCTCCCC 2040
TCTCTAATGA GCACCTCCAG CCCCAGATGC TTGCCTGGTT ACACGGTCAG GGACATTCCT 2100
GCCCCAATCC CCGACAGGCA CACATCATCC TAGGGCAGGG CCCTTCCTTG TGGGAACCAT 2160
CCATGCCCAG CTGAGGGCCT GGGGAGGACG AGTGCTGGGT GGGGGAGCCC TCCCTCTCTC 2220
TGCACACCCC TGGGAGCCCA CTTCTGTGTA TCATGGCATA CGTGGCATGT GCTGTGGTCT 2280
CTGCCATCAG CATCTAAACA GGCTCAGCCT CTGCTAGCCT CATGTACAAA CCACAAATTT 2340
CACCCAAAAA GTAAGTTCAC 2360