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

TagContent
EnhancerAtlas ID
HS141-00312 
Organism
Homo sapiens 
Tissue/cell
NB4 
Coordinate
chr1:26613420-26614720 
Target genes
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr1:26614546-26614557CCACACCCTGC+6.62
Myod1MA0499.1chr1:26613689-26613702AGGGACAGCTGCT-7.52
MyogMA0500.1chr1:26613692-26613703GACAGCTGCTG+6.14
Tcf12MA0521.1chr1:26613692-26613703GACAGCTGCTG+6.02
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_09234chr1:26600437-26620418CD14
SE_10276chr1:26609716-26620076CD19_Primary
SE_11598chr1:26601677-26620618CD20
SE_12127chr1:26609517-26619068CD3
SE_13098chr1:26613251-26615233CD34_Primary_RO01480
SE_14176chr1:26610126-26617625CD34_Primary_RO01549
SE_15660chr1:26609807-26618647CD4_Memory_Primary_8pool
SE_16821chr1:26610331-26617967CD4_Naive_Primary_8pool
SE_17222chr1:26613332-26618016CD4p_CD225int_CD127p_Tmem
SE_17706chr1:26601754-26619073CD4p_CD25-_CD45RAp_Naive
SE_18032chr1:26601635-26619607CD4p_CD25-_CD45ROp_Memory
SE_18600chr1:26600628-26620343CD4p_CD25-_Il17-_PMAstim_Th
SE_19301chr1:26601729-26619077CD4p_CD25-_Il17p_PMAstim_Th17
SE_20500chr1:26609324-26619072CD56
SE_21239chr1:26609862-26619058CD8_Memory_7pool
SE_22719chr1:26601924-26619047CD8_primiary
SE_24040chr1:26613586-26613984Colon_Crypt_2
SE_26906chr1:26613419-26617713Esophagus
SE_31060chr1:26610152-26618849Fetal_Thymus
SE_31862chr1:26613453-26614342Gastric
SE_31862chr1:26614480-26617883Gastric
SE_40404chr1:26609226-26616392K562
SE_41449chr1:26613365-26617866Left_Ventricle
SE_42616chr1:26613355-26618804Lung
SE_50183chr1:26601943-26618863Sigmoid_Colon
SE_52659chr1:26613372-26618804Small_Intestine
SE_53610chr1:26609706-26619005Spleen
SE_55161chr1:26613407-26618780Thymus
SE_62762chr1:26609498-26620090Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12661388726614371
chr12661347026614562
Enhancer Sequence
CTCAGGTGAT CCGCCCGCCT TGGCATCCCA AAGTGCTGGG ATTACAGGTG TGAGCCACCA 60
CGCCAGGCTG AGGCAGGGGT TATTTAGTTC CATTTTACAC ATGAGGAAAC AGGCCCACAG 120
AGATGAAAAA TGACTCGTCC CAAGCCACTT GGTGAGAGGA GGAACTGGGA AGGGAGCCGG 180
GGCTGACTCT CAAGTCTGTT TCCCCCACCC ATCTGCACCA TCAGGAGAGG GAGGTCAGAA 240
GAGGGACAGA TGGCTCTCAG GGAGGATGTA GGGACAGCTG CTGGCCAGAA CAGATATGGG 300
ACAGACCTTA GGTTGTGCAA CTATTTCTGG GTCACAGACC CCTTTGAGAA GCTGACAAAG 360
CTCTGGCCTC CTCTTCTGAA ACACGTGTGG CGCATACAGC TGTGTTCTGG CTTCAGGGGA 420
GAATACGGAG CGGTGGGGAC AGCCGTGACA GACAACAGAG CAGAAAGGTG GAGGGCAGGT 480
AGATGCTGGC TGGGTACAGA CCAGGGGCCT GTTCTGTCAT CTTTGATGGG ACCTGGCCCC 540
CAAGTAAGTC ATCTGTTTGG GTGTGCCCTA CAACACACCA ATAACTTTTG GGGCCTCAGA 600
GAGGCTGTTT TTCAACAGGA CAAGCAGGCT GCGGCAGGAT GTGGGTCAGG GCTCTGGGGA 660
CCTAATTCCT TTCCTCTCAG TGGTGCAGTG GCTGTACCAG GGAGGTGCAG ATGTGTTTCC 720
TGTTGCTTTT GCAGCAGGTG AAATGGTAGG CCCCAGCTGG CCTTCTCCTC TCCCCTATAT 780
TTCCTACCAT TGAAGGGGCT ATACCTGCCC CCAGCCCCTC CGGGGGCTCC CCACATAGTC 840
CCTGAGATTC CCAGGAAAAA CTCGCCTAAC AGAATGATAC CAAGACACTT TTCTTTTAAC 900
AACTACCTTA AGGACAAATA GGCAAACCTA AAAACAATAG CAGAATAGAT CATCTCATAC 960
AATGCCTGCC TCAACCCTTT TTTTTTTTTT TCCGAGAAAG GGTCTCCCTC TGTCACCCAA 1020
GCTGGAGTAT AGCGGCACAG TCATGATACT GCAACCGTGA CCTCCCGGGT TCAACTTATC 1080
CTCCCACCTC AGCCTCCCAA GTAGCTTGGA CCACAGGCAG GCATCACCAC ACCCTGCTAA 1140
TTAATTTAAA AAAAAATTGT AGAGATGGGG TCTCGCTGTG TTACCAGGGC TCTGTCTTCT 1200
TTATAGATGG GGAAAGTGAG GCCCAGAAAG GTCAGATGAC ATGGCCTGAT CAGACCAGAC 1260
AGAGCCAGGA AGAGCACCAA ATACACCAAC TCCTAATTCA 1300