EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS190-09730 
Organism
Homo sapiens 
Tissue/cell
Treg_cell 
Coordinate
chr4:10110530-10113470 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Myod1MA0499.1chr4:10112246-10112259AGCAGCTGTCCCC+7.04
MyogMA0500.1chr4:10112245-10112256CAGCAGCTGTC-6.14
TCF3MA0522.2chr4:10110751-10110761AACACCTGCT+6.02
Tcf12MA0521.1chr4:10112245-10112256CAGCAGCTGTC-6.02
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_01734chr4:10107077-10115538Aorta
SE_02758chr4:10109930-10111905Astrocytes
SE_04459chr4:10105408-10112471Brain_Anterior_Caudate
SE_05471chr4:10107753-10111919Brain_Cingulate_Gyrus
SE_08364chr4:10105438-10111735Brain_Inferior_Temporal_Lobe
SE_09623chr4:10105351-10111775CD14
SE_09623chr4:10111963-10114483CD14
SE_12329chr4:10110261-10111095CD3
SE_14886chr4:10105405-10112347CD4_Memory_Primary_7pool
SE_16236chr4:10110302-10111743CD4_Naive_Primary_7pool
SE_17168chr4:10110377-10111044CD4p_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_21402chr4:10109674-10111951CD8_Memory_7pool
SE_22779chr4:10093720-10112946CD8_primiary
SE_23672chr4:10109741-10112337Colon_Crypt_1
SE_23672chr4:10112538-10113532Colon_Crypt_1
SE_26123chr4:10104074-10111938Duodenum_Smooth_Muscle
SE_27018chr4:10105236-10112495Esophagus
SE_32010chr4:10107854-10111601Gastric
SE_37776chr4:10105574-10112955HSMMtube
SE_38833chr4:10106987-10111433HUVEC
SE_39084chr4:10108404-10111446IMR90
SE_41136chr4:10105238-10111825Left_Ventricle
SE_42597chr4:10105406-10113504Lung
SE_45147chr4:10110549-10111045NHLF
SE_46972chr4:10108380-10111760Ovary
SE_46972chr4:10111763-10112409Ovary
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_55072chr4:10109582-10111358Stomach_Smooth_Muscle
SE_69074chr4:10110445-10111967H9
SE_69074chr4:10111976-10114140H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr41011212310112391
chr41011296010113278
Number: 1             
IDChromosomeStartEnd
GH04I010091chr41009329910113947
Enhancer Sequence
ACATCATTTG TGCCCCACCT GCCTTCTGTA CTACGTGGAC ACCAGAGTGG GGAAGGTTCA 60
CACTTGATTC ACCATAGCAG CTGCCAAATA CCGACAAAGA CCAGAACTTG GCTGGAGCCT 120
GGTAGCTGTT TATCAAGAAA CAAATCCCCA CCGGCCACTT ACTATTCACT CTCAGACAGG 180
CCCTGGGTGG GCCCCTCAGT GGATTCTCTT TGAAACCTCA CAACACCTGC TGTAAGGAAG 240
GTAACCTCAT AATCCCACAT GACAAAGAAA CCAAGGCAGA CACTGGGCGA TACGCCCCAG 300
GCCACCCAGC TGTTAAGTGG CAGCGCCAGA CCTGAACTCA GGGCCAGTTG CTGACTCACC 360
TGGGTTATGA GCATATAACT AACAGCACGG TGAGTCAAGG GAGGTAACAA ATGCTCAACA 420
CCTTCACACA ATCCCAGGTC ACGTCACTGC AAATCAGGGA CCATATGTGG CGGCCTTTAC 480
TCCTCCCTGT GGTTTTGTTG TCTTCCTTAC GGTTGGTCTC AATGTTAGTG TGATTCTTTA 540
ATACAGAGAA TAAAGTCTGC ACTGGCCAAC CAGCTGTGTG CTTCCAAACA GTGTACAGGC 600
AGCTCCTTGA GCTGGCTGAG GACGGGGTGG TCACTCACAG GCCGCCATGC CCTGAACGAC 660
TTTCCCCTCC TGCCTCCCAG CTCAGCCTCA GATGCCTTGA AACAGGCCTG GGGGTACTCA 720
CCGTGTGGCC CTGCACAGCA GCACCCCTCA TTGGACTACG TGTGAGCGGG ACACCACCAC 780
CTCCGTTTTC AGTCTTCCCC TCTCCTACTC CCCACCCAGG GCCCACCAGG GCCTTAACTG 840
ATGAGTTGCA AAGGTAGACC TGGGGGTGGC TCCCAGGGTT CAAATTCCAG CACCTTCCAG 900
AGGTTCAGCA TCCTCACCTC TCAAAAGAGA GATGAGGGTA TCCACCCAAC AGGGCAGTCA 960
TGAAGACAAG AGCAGAGGTC CCTGCCAGGG CCCAGACAAC CTTCTGAAGA TGCTTTACGA 1020
ATTAGCTCCG TTAAATCTTA CACTGATCCC ATGATAACAT TCCTCCCACT CTCGCAGGCA 1080
TGGAAACAGA AGAGGCAAGC ACACCAAGTT TCAGCCACAG ACCAGCACAA AATACACTCA 1140
ACAAAGAACA GAGAGGTGCT CAGGGGTATA CACTGGATTG GACAGTGGGG CGGGGGTAGG 1200
GGTGGGATGC TGGCCTTTCC CTGGAGAGCA GGCAGGACCC ATACGTAGAA GTGACAAGCA 1260
AGGTGACCAA AGCTAAGGAC CCACAGGTCT AAGGAGCAGG CACATCGCCA GGGCAGGGAG 1320
TGCCTGCCCA TCACTGAGAC GGCGAAGAGA CGCACACAGG GCCCTTTCCT GTGTCCACAG 1380
CTGTCCCTAA CAAGGGCCTT GCAGAAGGTG GAGGTCACTC TCCAAAGAAG CATCTCCAAC 1440
TACTCTTGGG CAAGGCCATC TCTCCAGTAG TCTTACGCAT GAGGCTAAAC CTCTTCTCTT 1500
ACCTCAAAGA TGGCTTCAGT ATCCCTCCCG TTACCTCCAA CAGGGCAAGA AATGTACCAA 1560
AAGCAACACA CAGGAGGCCA CAGTGGGGCT GAGAGGACCC AGGTACACAT GCTGTTTCCT 1620
GCCTGGTTTC TCCCCACCTC TGCCGTGTGT CTCAACGCTC CTCCTGGAGA ACTCTTATTC 1680
ATCCTTCAAG ACCCAACTCA AATGTGGCAC TTCTCCAGCA GCTGTCCCCG CTCTGTGGCA 1740
CAGCTGGCTC CTCCCTCACA TTCCCAGAGC ACCCAGGGCA TTGTTCTTTT GAAGCACTTA 1800
ACCTGGTGCC TTCGAAGGTT CTTTACCAGA GTTTTCAACC TTGGTACCCC TGGCATTTGG 1860
GGCTGGACAG TTCTTTGTGG AAGGACGGCC ATGTACCTTG TCGGATGTTT GGCCACAACC 1920
CTGACTTCAG ATACCAGTGG CACAAAAATG TCTGCAAACG TTGCCAGATA TCCCTCAGGG 1980
GAATGAGGTG GGGGAAATTA CCCCTCCCTG AAAATCACTG ATTTTAATCC TGGTCCTCTG 2040
TGGCTTAGGG TATGGCTTGC CAAGACAGGG GCTTAGTGAA CATGTGTGGG AAACGTGAGA 2100
GCCAGAGATG GCTGCACCAC GCAACGGAAC CTGCGCTGAC GCCGCCTTCA TCTTTGAGCA 2160
GCTTCCTAAT TGGCTTCCCT GCCTCAGATC TCAGATACAG AACTTCTCCT TACCGTAGGC 2220
TGGATCTGAT TACTTGTCTG TGAGACCTCT GAATGGCTCC AGTGGCCTTC AGAGCAGGGC 2280
TGCGCTATGG TAGGGCTGTG TGAGCCACCT GCCACCACTG CACACCAGCA CTTCTCAGCC 2340
TGGGTCCTGT CCACTCCCCT CACGCTCAGT GCCACAGTAA CAGCCCATAA GCACCCGGCC 2400
CTTCGGTCCT CCCAGATGTG GTCCCATCTG CAGAAGCCCA GCGTCCTGAC TGGCACCTGC 2460
AGCCACTCAG ATTCTCCTGA GATGAAGGCC CCCCACCACC CTCTGCTTCC CCTGCCATCA 2520
GGTGGTCAGA CTGAAGGCCT AGAGGTTCCT GGCTCTGCAC CTGGCAGGCG CTGCTGCCAG 2580
CTCGTTTGCA CCCAGGTGAT AATCCAACGC ACCACTTCCT TCTGCCACCT AGAGTTTATT 2640
TCACTCCCAC CCAGGACAGT GAGCTCCATG TGGGCAGGGC CTCCATCCTG CACCCCCACA 2700
GGCCAATGGC CATCTGGATA CACGCAGGTA GTCAGCAGGC GTCCAATTCC GGAGAAGCAG 2760
CTAGGTCAGT CCTCAAGCCC TCTGTCATGC CACCATTACC CCCAACCCGC AGGAAACACA 2820
GGTGAGTCCT CTGCATGTGA ATGGTGGCAG CTCACACCAA GGGAAACCAA GAGTGAGCCC 2880
AATACCCTCC CCAACCCCCC ACTTGGTCTG CCCCCTGTTC AAGGAGAAAA GTCCACTGAT 2940