EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS034-04462 
Organism
Homo sapiens 
Tissue/cell
ECC-1 
Coordinate
chr10:126381730-126383030 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxo1MA0480.1chr10:126382824-126382835TGTAAACAGGA-6.62
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_00867chr10:126382460-126383468Adrenal_Gland
SE_03059chr10:126382298-126383494Bladder
SE_03136chr10:126382036-126384047Brain_Angular_Gyrus
SE_03854chr10:126381278-126400264Brain_Anterior_Caudate
SE_04762chr10:126349641-126400539Brain_Cingulate_Gyrus
SE_05766chr10:126349634-126432936Brain_Hippocampus_Middle
SE_06675chr10:126352052-126400411Brain_Hippocampus_Middle_150
SE_08784chr10:126382044-126382200Brain_Mid_Frontal_Lobe
SE_08784chr10:126382452-126382673Brain_Mid_Frontal_Lobe
SE_10231chr10:126381919-126383539CD19_Primary
SE_11826chr10:126382208-126388040CD3
SE_14406chr10:126380885-126399243CD4_Memory_Primary_7pool
SE_15467chr10:126382226-126387936CD4_Memory_Primary_8pool
SE_16286chr10:126382026-126386368CD4_Naive_Primary_8pool
SE_16956chr10:126382595-126388103CD4p_CD225int_CD127p_Tmem
SE_17772chr10:126381322-126400326CD4p_CD25-_CD45ROp_Memory
SE_18306chr10:126381215-126398866CD4p_CD25-_Il17-_PMAstim_Th
SE_19113chr10:126382326-126383531CD4p_CD25-_Il17p_PMAstim_Th17
SE_19980chr10:126381909-126398610CD56
SE_20757chr10:126381300-126387847CD8_Memory_7pool
SE_22300chr10:126379671-126399931CD8_primiary
SE_26558chr10:126381993-126383146Esophagus
SE_27648chr10:126382212-126383978Fetal_Intestine
SE_28609chr10:126381970-126384134Fetal_Intestine_Large
SE_29582chr10:126381904-126383328Fetal_Muscle
SE_30910chr10:126381933-126384317Fetal_Thymus
SE_31435chr10:126381892-126383753Gastric
SE_40602chr10:126381203-126384381Left_Ventricle
SE_42109chr10:126381867-126383965Lung
SE_48059chr10:126380077-126384160Psoas_Muscle
SE_48558chr10:126381201-126381880Right_Atrium
SE_48558chr10:126381927-126383988Right_Atrium
SE_50103chr10:126381991-126384073Sigmoid_Colon
SE_51170chr10:126380959-126384345Skeletal_Muscle
SE_52350chr10:126381896-126384334Small_Intestine
SE_53300chr10:126382058-126384299Spleen
SE_55093chr10:126382110-126382658Thymus
SE_55093chr10:126382723-126383425Thymus
SE_58522chr10:126367014-126434794Ly1
SE_62212chr10:126285528-126438541Tonsil
SE_65502chr10:126381338-126383699Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10126382372126382711
Number: 1             
IDChromosomeStartEnd
GH10I124691chr10126380158126399793
Enhancer Sequence
TCTCTTCCCC ACTGTTGAAA AGCAGGCACG CCGGGCGCGG TGGCTCACGC CTGTAATCCC 60
AGCACTTTGT GAGGCTGAGG CAGGCGGATC ACGAGGTCAG GAAATCAAGA CCATCCTGGC 120
CAACATGGTG AAACCCCGTC TCTACTAAAA ATACAAAAAT TAGCTGGGCG TGGTGGCACA 180
CGCTTGTAAT CCCAGCTACT TAGGAGGCTG AGGCAGGAGA ACTGCTTGAA CCTGGGAGGC 240
GGACGTTGCC GTGGGCCAAG ATCACACCAC TGCCCTCCAG CCTGGCGACA GTGAGACTCT 300
GTCTCAAAAA AAAAAAAAAA AGAAAAGCAG GCACACCTCA GATGAAATCT CGCTGCCTGG 360
GTGGAGTGCA CTCCCAGTTC ATGGAGCACA CGGAGGACTG GAGAGGTAAC CTGAGCTTCC 420
ACTAGACAGA GTGCACGGGG TAAGGCTCCT GACTGCTGAC ACCCGCTCCG CTCCAGCAAG 480
CGCAGGAAAG GGATAGAGGT GGGAGGGAGG ATGTGTGCTA GTGTGTGGCC GTCTCCTTAA 540
ATCCTCACAA CTTGCAAACT GAGGAAACCT AGCCGGGAAG ATGGGGTGGT ATCCCCATAG 600
CTCAAGGGCC TCCACATCTC ACGGGAGTTG GCCTAAGCAG TGCAGAATTC ACTGTTCGTT 660
GATCTTTCTC CTCCACCAGA CAGAAAGCTC CCTGAGAGAA GGGGCAGGGT CTGATTCACT 720
CTATCCCTCA CCAGGTGCCT GACACACAGC AGGTGCTCAA GTCATATCTA TGACAGCAAG 780
CCACTGAAAA TGAAAACAAA CTGCAGTCAG TGAAACACGT CAGTGATGCA CAGCCATGCA 840
GGTCAGGGTT TTCCTGAATT AGGGAGGGGC CGACCAACAG AAAGATGAGA CCCATGGAGA 900
GAGAGCAGCA GAGGAGAACA AGGGGACTCC ACAGACCTCC CACCAGTACA ACGGCTCCCC 960
GCTTCTCCCT CTGCTGCCTG GCAGTGCCCT GGCACTGTCC CACAGAGCAG AAGGAAGACA 1020
GGACCCTGCT GAAGAGGAGA AGAGCCTGGG ACGGAGGCAT TGGGACCCAG CCAGCACTTC 1080
CTAAAGAGCC ACTCTGTAAA CAGGAGTCTG CAGACACAGC GTAGTCCCTC CTGGAAACCA 1140
TGGCCTCCCC GGTAGAAAGC AGGTTGCTGG GCTCTGCAGC CTCCGATAGA CTCTCCTGGG 1200
CCATCTGGAC TTTTTCCCAC ACACCTCCCT TCTCCGGGGC CTCTGCCTTG GTCTCTGGGC 1260
CTCAAGACCT GGCCCTACAA GGGCGACTCT CTCTGTCATC 1300