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

TagContent
EnhancerAtlas ID
HS113-26923 
Organism
Homo sapiens 
Tissue/cell
Keratinocyte 
Coordinate
chr4:10115200-10117730 
Target genes
Number: 4             
NameEnsembl ID
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6MA0463.2chr4:10116379-10116395CGGCTTTCTAGGAATC+6.87
KLF14MA0740.1chr4:10117609-10117623GAGGGGGCGTGGCG-6.28
KLF16MA0741.1chr4:10117611-10117622GGGGGCGTGGC-6.62
PBX1MA0070.1chr4:10116731-10116743GCATCAATCAAA+6.32
SP3MA0746.2chr4:10117610-10117623AGGGGGCGTGGCG-6.82
SP8MA0747.1chr4:10117610-10117622AGGGGGCGTGGC-6.92
SPICMA0687.1chr4:10117035-10117049TGCTTCCTGTTTTT-6
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_01734chr4:10107077-10115538Aorta
SE_01734chr4:10115764-10118561Aorta
SE_02758chr4:10116522-10118498Astrocytes
SE_04459chr4:10115514-10118183Brain_Anterior_Caudate
SE_05471chr4:10116532-10119955Brain_Cingulate_Gyrus
SE_08364chr4:10116063-10118051Brain_Inferior_Temporal_Lobe
SE_09623chr4:10114621-10120741CD14
SE_12329chr4:10117297-10118067CD3
SE_14886chr4:10116769-10120864CD4_Memory_Primary_7pool
SE_16236chr4:10116827-10120999CD4_Naive_Primary_7pool
SE_17168chr4:10116550-10120562CD4p_CD225int_CD127p_Tmem
SE_17601chr4:10114889-10126849CD4p_CD25-_CD45RAp_Naive
SE_18041chr4:10114662-10121218CD4p_CD25-_CD45ROp_Memory
SE_18604chr4:10090926-10121361CD4p_CD25-_Il17-_PMAstim_Th
SE_19188chr4:10115095-10120578CD4p_CD25-_Il17p_PMAstim_Th17
SE_21402chr4:10116230-10120367CD8_Memory_7pool
SE_22779chr4:10115919-10118581CD8_primiary
SE_23672chr4:10116381-10120266Colon_Crypt_1
SE_24384chr4:10116641-10120117Colon_Crypt_2
SE_26123chr4:10116045-10120882Duodenum_Smooth_Muscle
SE_27018chr4:10115010-10115663Esophagus
SE_27018chr4:10116322-10121117Esophagus
SE_30028chr4:10116946-10118234Fetal_Muscle
SE_32010chr4:10116541-10120433Gastric
SE_37776chr4:10116140-10119896HSMMtube
SE_38833chr4:10115045-10120109HUVEC
SE_39084chr4:10116274-10118476IMR90
SE_41136chr4:10116270-10120034Left_Ventricle
SE_42597chr4:10116137-10118617Lung
SE_45147chr4:10114992-10115526NHLF
SE_45147chr4:10116298-10118154NHLF
SE_48189chr4:10116071-10119846Psoas_Muscle
SE_48835chr4:10116297-10118603Right_Atrium
SE_50444chr4:10116206-10121732Sigmoid_Colon
SE_51167chr4:10114584-10120461Skeletal_Muscle
SE_52707chr4:10116274-10118625Small_Intestine
SE_55072chr4:10116777-10121661Stomach_Smooth_Muscle
SE_66345chr4:10117182-10117874Jurkat
SE_69074chr4:10116185-10118650H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr41011680110117310
Number: 1             
IDChromosomeStartEnd
GH04I010113chr41011499310115663
Enhancer Sequence
ACTCCAGCGA GTGTTGTGAA CAGACCCCCA GGGCAACAAG GGTGAAAGCA AGGAGACCTG 60
TTTGGTTTTC GGGAGTCTGG GGGCAATAAG TCAGGTGGGG GAAGATAGCT TAGTCGTGGG 120
TGGAGGCAGA GGAAGCCAGG GAAATCTGTT AGATTCTGAA GATACTTTGA ATGTGGAGTC 180
AGAAGGATTT ACTAAAATTA AAATGTGGCG CAGTAGCGAA GCAGAGAGTG AAACAGGAGT 240
CCAAGGTTTG GGGCCTGAAC AGCTGGAGGA ACGGTGTTCC CTTTTAGGGG AAGAGCACGT 300
GGGAAACACA AATTTGGCTT GGAGTATGTA TGTTGAGTCT GAGATGTCAA TGAGACATGT 360
TAGATCTTCC ATGATCTGGT CCTCCATTTC TTCCCTCTTC CCTCCCTGAG CCTGCATTCC 420
AAACAGACCA TCATCCTTCC TGAACGGTCA TGCCAATTCA TGTCACTTTT TTTTCCAAGA 480
GTACTTTGCC CTAAAAAAAA TCGTACCCAC CTTTACTTGA GTACCCAGTC CACCCATCCA 540
ACTAACAAGA GACTCAGTGC CTGATCTACA TCCAGCCCAG GGAGGGCTAT ATTAGTAGCA 600
TCTCGTGCTG ACCTGGCATT GCAGAAACTT AAAAATAATT GAGAAGGGAA ACAGGGTAAC 660
CCCTGAGAAG AAAATGGCAA ACCACGGGGA AGGGGTAAGA ATACAGAGCT CAGAAACAGG 720
CAGAATGGGT TTCACAAGCT GGGAAATGCT TTCTGCAAAG GGGTGCCTGT CCCTGAATGA 780
CCACTCCATT AGAAGCAGCT CCAGTTACTG GCCTGCCTCA CCTTGCTAAG TCTGACTCCT 840
CTTTAGAGTA ACGGACCCAT GTGGGGTGGA AAGAGATGCT ACAGTTTAAG AAGCTATCAC 900
AGGGCCAGAT GCACAGCAGG TACTTTATGT GAGGCCCCCT CCCTGGAAGT CAATGTGGAC 960
TGCAACGACA GGGAAGGCCT GGTTAGGGGC AAAACGAAAT ATCCTACTGC TCTGTATCCG 1020
AGGACGTGTT AGTGGATTTT ATTTGCCAAA CTACTAAATA TCTCTTTAGG GTTGTCTCAA 1080
TTTTTATTTT CTCAAAAGCC TCAGGACCTG CCTTCGGAGA CTTCCAGATC ATTACCATTA 1140
GATCCCTGGT GATTTTCTCC AGTTCTAAGC AAGGCCCTTC GGCTTTCTAG GAATCTGTGT 1200
GACTAGCAAG TTGTTAGCAC CTTCAAAGCA CATTCACACC CGCCCACCCC CTCATTTGAG 1260
GGGCCCAGCA ATCCAGGGCA GGTAGAGCTC TGTCTTCCAG CAGAGGAACA GCAGCGACTG 1320
CCTGGGTTAA CGAGACAGAT GCGGGCAGAG CCAGCAGCTC TTCGGACCAA GAGGCTTCTC 1380
CTTTCACAGA GAAGGAAACT GAGACCCAGA GACCCCTTCA TTCCCTCAGC CAGTTGCTGG 1440
CCTCCTGGAG GGCAAGTGTG TCCGATCAAC AGTCCCAACC TACCAAGGGA AATCAGGCTG 1500
ACTTTAAGTT GACAACCCTT GTATGCCTAT GGCATCAATC AAAACATACA TCTTTGTGCC 1560
AGCCGCCCCC ACTAAGCACA GCACAGGAGA AATCACCCAA TGGCCGGGCC GGCACCTCCA 1620
ACTCCCACCC CACCAATTCC ATCACTCAGG CTGAGGAAGG GAAAAGCAAA ATTTAAGCGT 1680
GTAACCCAGG AAGGGAGGGA GACTGACAGA CTGGGTCACC CCAACAATTA CAGAGGAATA 1740
ACATGAATTT GCAAGGATTT CCCAAGGAGC TGGCTCTAGA AGCCTTTTCA GCCTGGGTAC 1800
CGGAGGCTTG CAGAGAATGA TTCATGGGAA AACACTGCTT CCTGTTTTTG CTTTGGGGCT 1860
TAGATCCATG GTGGCAGATC TGGCTGGCCC AGAGGCCCGG GTGTTTTTCC GGGCTCTGCC 1920
ATACTGGAAG ACCAGGGTAT TAACAGCGAG TTAGCTGAGT GCCATTCCAT TCAGCAAGGG 1980
CTCAAAGTGC ACCAGGCACC GCTGGGCTTG AGGGACGCCA GCAGCTCATT CATTCCATCT 2040
GCCCAGCCAG CAGGCGAAGC GAGAGTGGTC ATCATCTCAT CATCTGTTTT ACAGACGAGA 2100
AAACTGGGGC TCAGAGATGC CCAAATCGCC AATCTTCTCA AGGTCACGCA GCGGCCGACC 2160
GGGTCAGTCT GATCCCTCAA ATCCGGAGCC CTTGCTTTTA AGGAATGAAC TAATCTAATC 2220
TCCCATCCAC GTACTAACCA GGCCTGACCG TGCTTAGCTT CCAAGATCAG AGGCGATCCG 2280
GCGCTTTCAG GGTGCTATGA CCGTAGACAG AAACGAACTA AGACTCAGTT TCCTCATCAA 2340
GAAGGAGCAG ACAAGGACCT GGGTGAATCT GAGGCCGGCT TCCGGGGCTC CGAGGTGTGG 2400
CTCCCGGTAG AGGGGGCGTG GCGCCCTCAC CCTCCCCGGG CCAATGGGCA GGAGGTGAGA 2460
AGTGGAGAGG AAGGCGAATT ATCCCATCCC AAGGTGGCTC CGGAGCAGAA CCGCGCCCGG 2520
GGTAGGGGGT 2530