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

TagContent
EnhancerAtlas ID
HS167-04524 
Organism
Homo sapiens 
Tissue/cell
Retina 
Coordinate
chr4:10115930-10117730 
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: 36             
IDCoordinateTissue/cell
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_27018chr4:10116322-10121117Esophagus
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_45147chr4:10116298-10118154NHLF
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
Enhancer Sequence
TTCACAAGCT GGGAAATGCT TTCTGCAAAG GGGTGCCTGT CCCTGAATGA CCACTCCATT 60
AGAAGCAGCT CCAGTTACTG GCCTGCCTCA CCTTGCTAAG TCTGACTCCT CTTTAGAGTA 120
ACGGACCCAT GTGGGGTGGA AAGAGATGCT ACAGTTTAAG AAGCTATCAC AGGGCCAGAT 180
GCACAGCAGG TACTTTATGT GAGGCCCCCT CCCTGGAAGT CAATGTGGAC TGCAACGACA 240
GGGAAGGCCT GGTTAGGGGC AAAACGAAAT ATCCTACTGC TCTGTATCCG AGGACGTGTT 300
AGTGGATTTT ATTTGCCAAA CTACTAAATA TCTCTTTAGG GTTGTCTCAA TTTTTATTTT 360
CTCAAAAGCC TCAGGACCTG CCTTCGGAGA CTTCCAGATC ATTACCATTA GATCCCTGGT 420
GATTTTCTCC AGTTCTAAGC AAGGCCCTTC GGCTTTCTAG GAATCTGTGT GACTAGCAAG 480
TTGTTAGCAC CTTCAAAGCA CATTCACACC CGCCCACCCC CTCATTTGAG GGGCCCAGCA 540
ATCCAGGGCA GGTAGAGCTC TGTCTTCCAG CAGAGGAACA GCAGCGACTG CCTGGGTTAA 600
CGAGACAGAT GCGGGCAGAG CCAGCAGCTC TTCGGACCAA GAGGCTTCTC CTTTCACAGA 660
GAAGGAAACT GAGACCCAGA GACCCCTTCA TTCCCTCAGC CAGTTGCTGG CCTCCTGGAG 720
GGCAAGTGTG TCCGATCAAC AGTCCCAACC TACCAAGGGA AATCAGGCTG ACTTTAAGTT 780
GACAACCCTT GTATGCCTAT GGCATCAATC AAAACATACA TCTTTGTGCC AGCCGCCCCC 840
ACTAAGCACA GCACAGGAGA AATCACCCAA TGGCCGGGCC GGCACCTCCA ACTCCCACCC 900
CACCAATTCC ATCACTCAGG CTGAGGAAGG GAAAAGCAAA ATTTAAGCGT GTAACCCAGG 960
AAGGGAGGGA GACTGACAGA CTGGGTCACC CCAACAATTA CAGAGGAATA ACATGAATTT 1020
GCAAGGATTT CCCAAGGAGC TGGCTCTAGA AGCCTTTTCA GCCTGGGTAC CGGAGGCTTG 1080
CAGAGAATGA TTCATGGGAA AACACTGCTT CCTGTTTTTG CTTTGGGGCT TAGATCCATG 1140
GTGGCAGATC TGGCTGGCCC AGAGGCCCGG GTGTTTTTCC GGGCTCTGCC ATACTGGAAG 1200
ACCAGGGTAT TAACAGCGAG TTAGCTGAGT GCCATTCCAT TCAGCAAGGG CTCAAAGTGC 1260
ACCAGGCACC GCTGGGCTTG AGGGACGCCA GCAGCTCATT CATTCCATCT GCCCAGCCAG 1320
CAGGCGAAGC GAGAGTGGTC ATCATCTCAT CATCTGTTTT ACAGACGAGA AAACTGGGGC 1380
TCAGAGATGC CCAAATCGCC AATCTTCTCA AGGTCACGCA GCGGCCGACC GGGTCAGTCT 1440
GATCCCTCAA ATCCGGAGCC CTTGCTTTTA AGGAATGAAC TAATCTAATC TCCCATCCAC 1500
GTACTAACCA GGCCTGACCG TGCTTAGCTT CCAAGATCAG AGGCGATCCG GCGCTTTCAG 1560
GGTGCTATGA CCGTAGACAG AAACGAACTA AGACTCAGTT TCCTCATCAA GAAGGAGCAG 1620
ACAAGGACCT GGGTGAATCT GAGGCCGGCT TCCGGGGCTC CGAGGTGTGG CTCCCGGTAG 1680
AGGGGGCGTG GCGCCCTCAC CCTCCCCGGG CCAATGGGCA GGAGGTGAGA AGTGGAGAGG 1740
AAGGCGAATT ATCCCATCCC AAGGTGGCTC CGGAGCAGAA CCGCGCCCGG GGTAGGGGGT 1800