EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS197-06339 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr13:114882970-114885710 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Znf423MA0116.1chr13:114883736-114883751GAACCCCAGGGGGGC-6.02
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_02428chr13:114883230-114885686Astrocytes
SE_06573chr13:114883575-114885498Brain_Hippocampus_Middle
SE_14520chr13:114884602-114885683CD4_Memory_Primary_7pool
SE_15834chr13:114884396-114885539CD4_Naive_Primary_7pool
SE_17059chr13:114884714-114885480CD4p_CD225int_CD127p_Tmem
SE_17352chr13:114883523-114898593CD4p_CD25-_CD45RAp_Naive
SE_17971chr13:114883611-114885613CD4p_CD25-_CD45ROp_Memory
SE_18337chr13:114883368-114885571CD4p_CD25-_Il17-_PMAstim_Th
SE_19216chr13:114883212-114885604CD4p_CD25-_Il17p_PMAstim_Th17
SE_20430chr13:114883859-114885479CD56
SE_22425chr13:114883341-114885626CD8_primiary
SE_24261chr13:114885036-114885377Colon_Crypt_2
SE_29941chr13:114883266-114885690Fetal_Muscle
SE_31056chr13:114883598-114885251Fetal_Thymus
SE_32435chr13:114883551-114885598Gastric
SE_37803chr13:114882968-114887163HSMMtube
SE_38174chr13:114882988-114888488HUVEC
SE_38982chr13:114883200-114885441IMR90
SE_43224chr13:114883365-114884058Lung
SE_43224chr13:114884064-114885591Lung
SE_44466chr13:114883199-114885342NHDF-Ad
SE_44821chr13:114883330-114885627NHLF
SE_46527chr13:114883282-114885490Osteoblasts
SE_47322chr13:114883133-114885548Panc1
SE_47981chr13:114884131-114884572Pancreas
SE_48488chr13:114884636-114885447Psoas_Muscle
SE_50252chr13:114883126-114885479Sigmoid_Colon
SE_52117chr13:114883228-114885582Skeletal_Muscle_Myoblast
SE_53247chr13:114883402-114885567Small_Intestine
SE_54100chr13:114883411-114885661Spleen
SE_56179chr13:114883397-114885474u87
SE_62671chr13:114874284-114928516Tonsil
SE_63914chr13:114883224-114885458HSMM
SE_67713chr13:114883397-114885474u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr13114883891114885086
chr13114883390114883869
Number: 1             
IDChromosomeStartEnd
GH13I114117chr13114882921114891675
Enhancer Sequence
GGGGTGCACA TCTGTGGGTG AGCATGTGCG TGAGGGGTGC ACATGTGTGA GGGGAGCACG 60
TGTGTGAGGG GTGCATGCAA TGCTTCTGTA TGCACATCTG TGGGTGAGCA CGTGTGTGAG 120
GGGTGCACGT GTCTGAGGGG TGCATGTGTG TGAGGGGTGC ACGTGTGTGA GGGATGCACG 180
TGTGTGAGGG GTGCATGTGT GTGAGGGGTG CACGTGTGTG AGGGATGCAT GTGTGTGAGG 240
AGAGCACGTG TGTGAGGGAT GCACGTGTGT GAGAGCACGT GTGTGAGGAG AGCACGTGTG 300
TGAGGGGTGC ATGTGTGTGA GGGGTGCACG TGTGTGAGGG GTGCATGCAA TGCTCCTGTA 360
TGCACATCTG TGGGTGAGCA CGTGTGTGAG GGGTGCACGT GTGTGAGGGG TGCATGCACA 420
CACACCTGTA AGCATGTGTG TGAGGGGTGC ACGTGTGAGG GGTGCATGCA CACGCACCTG 480
TGTGCACATG TGGATGTTGC CGTGTGCACG TGTGCACACC AAGTGTCCGT GAGTGCACGG 540
GAACAGCCGT TTAGAAGTGC CTTAATCTTC CCGAGCACAA TAGTAGCTCA CCTCTGCAAG 600
GAGGCTGAAA ATTCTCATTA TGAGTCTCAT AAATACGTGG CCACGTTCAT GGGTTTGTCT 660
TATTTATCCC TTACTCTATA ATAACTTGGA AGGCACAGCC AATATTTCCC TTATATCCTG 720
GGACAGCCCC AGTTCATGGC TCCCGACGAC TGCAGCTGCC TCCTGGGAAC CCCAGGGGGG 780
CAAACTCAGG CCCACCCCCG CCTGTGTGAC TCAAACCCCC CAGCCAAGTG CCTGTGGGAG 840
GACATTTTAG TGGGTGGGGA AGCTTCTGAA AAATCACTTT ACTCTAACTA ATATTTGTAA 900
TTAACACATC AAGTAAAACT AAAAGCTTTT GCCTTGCCGT TGTTGCCTTT TGGTGGGTGA 960
CCTCAAAAAG TCATCCATCT CACACTGACT CTATCACATC CCAACTCTAG CCCCAAATCC 1020
TAATAAACAC ACCAGTTAAG AATGCATGGC ACATTTTTAC AAGCCTCACA ACTTTCTGAT 1080
TAGATGCATA GAAATGTCCC AAATATTTCT GAAATATTTT ATTTGAAAAC CGATGTCACC 1140
GCCACTTTTA AGCCACAGGC ATTACACTAA AATCTGGACT AGCGTCTAAG CAAGTGGCAG 1200
CTTTTGAGCT CCGCACACTC CGTGTGACCA TCCACAAATC TATGATGAAT TATTAACCAG 1260
ACCAGGCTAG CCCACTGCCT GGCCTTCTCT GCTGAAAGTC AGCAGCTGTA TCCTGCCTGA 1320
AAAACACCAG CATTCTTGTG TTCATAAAAC CCGCTGGTTC CAGTGCAGCT ACCCAGAGGG 1380
AAGCCTTGGG TGTGGGCAGC GACAGGGGTG TGGGTGCCAC CGTGGGGTCC CCCAGAAGGA 1440
AACCAGGGGA GCACAGAACT AAATGGTCAC CCATGACAAT GAATCGTGAT CTGGTGGGAA 1500
GAAATCAAAG TGCTTTTATT TGGAGATGAA ATTGGCTGCC TGCCCCTCCC TCTCCACCCC 1560
CCGCTTTCCT CCTGACCCAC CCACCCCAGC TCTTTTCCCC GGCCTGGGAA GGGCACATGG 1620
AGGGCAGAAA GGGCTTCCCT AAAGAAAACA CAGAAATACA CTTTATAAAG CAAAATAAAC 1680
TTAAAAAAAG GCACTTAGCA AAAATGTAGT GAGAAGTGTT TTTTCCTTTC CAGTCTTTCA 1740
TTTTCACTCA GCATTTCCAT AAACACATTC TTGGGTCCAA ATGCTGAGAA ACTCTTTCTC 1800
TAAATACTGG AGGAGCGCTA AATGGAGCAG GAAATGATGG AGAGAGAAAG GAATGCCACT 1860
GATTCCAGAC GGATGGGACC AGCTGGGGAA TTCAGGAAGC GGTACGGAGG TCCCGGAGAC 1920
AACTGCTCAC GCCTCTGAGG GGCCGATCGC TCAGGATCCC CCAGCAGCAG CGAGAGAACC 1980
AGCAGGGCCC CCCTCCCCTC TCCAGCCAGG CGTCGATCAG TGCCCCCCTC CCCTCTCCAG 2040
CCAGGCGTCG ATCAGGGCCC CTCCCTCTCT CCAGCCAGGT GTCGATCAAG TCCTCACCTT 2100
CTCTCCAGCC AGGCGTCGAT CAGGGCCCCT CCCTCTCTCC AGCCAGGCGT CGATCAAGTC 2160
CCCCCCTTCT CTCCAGCCAG GCGTCGATCA GGGCCCCCCC TCCCTCTCTC CAGCCAGGCG 2220
TCGATCAGGG CCCCCCCTCC CTCTCTCCAG CCAGGCGTCG ATCAGCGCCC CCCTCCCCTC 2280
TCCAGCCAGG CGTCGATCAG GGCCCCTCCC TCTCTCCAGC CAGGCGTCGA TCAAGTCCCC 2340
CCCTTCTCTC CAGCCAGGCG TCGATCAGGG CCCCTCCCTC TCTCCAGCCA GGCGTCGATC 2400
AGGGCCCCCC TCCCCTCTCC AGCCAGGCGT CGATCAGGGC CCTCCCTCCT CTCTCCAGCC 2460
AGGCGTCCAT CAGGGCCCCT CCCTCTCTCC AGCCAGGCGT CGATCAGGGC CCCCCCTCCT 2520
CTCTCCAGCC AGACGTCGGT CAGGGCCCCT CCCTCTCTCC AGCCAGGCGT CGATCAGGGC 2580
CCCTCCCTCT CTCCAGCCAG GCGTCGATCA GGGCCCCCCT CCCCTCTCCA GCCAGGCGTC 2640
GATCAGGGCC CCCCTCCCCT CTCCAGCCAG GCGTCGATCA GGGCCCTCCC TCCTCTCTCC 2700
AGCCAGGCGT CGATCAGGGC CCCTCCCTCT CTCCAGCCAG 2740