EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-11468 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr17:21178450-21180030 
TF binding sites/motifs
Number: 13             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXC1MA0032.2chr17:21179912-21179923TATGTAAATAT+6.62
KLF14MA0740.1chr17:21179211-21179225TGGGGGGCGTGGCT-6.26
KLF16MA0741.1chr17:21179213-21179224GGGGGCGTGGC-6.62
Klf12MA0742.1chr17:21179223-21179238CTGGAGGGCGTGGCC-6.16
NFAT5MA0606.1chr17:21179959-21179969ATTTTCCATT+6.02
NFATC1MA0624.1chr17:21179959-21179969ATTTTCCATT+6.02
NFATC3MA0625.1chr17:21179959-21179969ATTTTCCATT+6.02
NFYAMA0060.3chr17:21179174-21179185AGCCAATCAGA+6.32
NKX2-3MA0672.1chr17:21178643-21178653ACCACTTGAA+6.02
RREB1MA0073.1chr17:21179559-21179579CCACCCGCCACCCCCACCCG+6.13
SP1MA0079.4chr17:21179212-21179227GGGGGGCGTGGCTGG-6.27
SP3MA0746.2chr17:21179212-21179225GGGGGGCGTGGCT-6.74
SP8MA0747.1chr17:21179212-21179224GGGGGGCGTGGC-6.44
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_10839chr17:21178719-21180066CD19_Primary
SE_12406chr17:21178953-21180042CD3
SE_18098chr17:21178375-21180651CD4p_CD25-_CD45ROp_Memory
SE_19017chr17:21178448-21180171CD4p_CD25-_Il17-_PMAstim_Th
SE_19511chr17:21178481-21180011CD4p_CD25-_Il17p_PMAstim_Th17
SE_20528chr17:21178474-21180192CD56
SE_22813chr17:21178431-21179952CD8_primiary
SE_23898chr17:21178691-21179218Colon_Crypt_2
SE_23898chr17:21179250-21179741Colon_Crypt_2
SE_25244chr17:21178581-21179903Colon_Crypt_3
SE_27120chr17:21178642-21179696Esophagus
SE_31667chr17:21178677-21179722Gastric
SE_41043chr17:21178140-21179815Left_Ventricle
SE_41861chr17:21178592-21179801LNCaP
SE_42495chr17:21178575-21179836Lung
SE_47630chr17:21178994-21179563Pancreas
SE_48170chr17:21177698-21180005Psoas_Muscle
SE_49589chr17:21178701-21179228Right_Ventricle
SE_50520chr17:21178624-21179779Sigmoid_Colon
SE_51538chr17:21177951-21180065Skeletal_Muscle
SE_52785chr17:21178711-21179735Small_Intestine
SE_53759chr17:21178517-21179883Spleen
SE_58432chr17:21170318-21277177Ly1
SE_61419chr17:21170524-21296554Toledo
SE_65398chr17:21178443-21180096Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr172117910021179414
chr172117918321179800
Number: 1             
IDChromosomeStartEnd
GH17I021274chr172117825321180112
Enhancer Sequence
GCACGCCGGG GGCATACTGG CTGCCCGCCC AACAGATGTC TGGATCAGTC TGAATCCTGG 60
GCACCCGGGA GAGGAAATGA ATTCCCTTCA TCAGCGGCCT CGAGCCCCCA GCAGTCCTCC 120
TCCACCCGGG GACAAATTCT TCTCTCCCCC CAAGAATGTT TGCAATCCTT CGGATGGCAG 180
TTTTCCAAGA CCGACCACTT GAATGTCCTC TCTACCCTCA TAAAAGCAAG ACCTGTTCCT 240
TGCTGGGAAA GCATGGGGTG GGTGATCGTC TTCAACCTTT AAAGGGCTGG ACCCGTAGCT 300
GCTGCACCCG GGGGCACAGC TGACGGGAGA GGAGAAGCGG CCTCTTCTCA GCATGGGGAT 360
GTGGGGAGCC GCTCAGGGAG AGAAAACGAG GCCTTTACAG CACCGGTTTA ACAGCCTCGG 420
CCACGCATCT GCCCGCACAG ATCTAAGGCT TGGCTTCGGG TCCGGCTCCA CGCCTGCCCC 480
ATGTCCCCAC GGTCCGCGGC CCTCGGGAGG CCCGGCCCTG GGGGCTGAGC TCTGCCCTGG 540
GACCGAAGGC CACTCTCCCA GCCAAGGCCG GAGGGCTCTG CCCTGGGCAC ATGCGCCCCA 600
TCCGCCTGCC CTGAGCTGAC CCCGCCGCTC CACACCACCC CACTCGCGGC TGAAAAGCTG 660
AAGGCAGCCG CACACTCGCC CTTGCAGCTT GCCCTGCAGC CCGCGCGGCC ATGTGAGCAA 720
GCGCAGCCAA TCAGAGGCTC GCCCTGGACT CCGTCCCGGG CTGGGGGGCG TGGCTGGAGG 780
GCGTGGCCGG GCGGTACCCG CGGCGTCTCT GCGCTGCCGC CTTTGCTTGC GCGGCTGTGT 840
AGGGGGTTGT GGCGGGCCGG AGAGTCCCCG AGTGACTTAA CATTCTCTAA AAATACCCCA 900
TTTTTGAACT TCGACGACCT GGGTTGGCCT GCTCACTCTG TGTCCCTGCG CTCCTCTGCT 960
TCTCTGCTCC TTCGGTCTTG TGTGCTGGGG ACACGTGGGC CTTTCCAGTT CCCTGCAGCC 1020
ACCTTTGGTC TGTAGGAAGG CAGTGGCGCA GGGAGCGGTG GGAGCCCGGG TCTGCAGGGC 1080
TCAAGGTGGC GACGGCGAAG CGGTCTGCCC CACCCGCCAC CCCCACCCGC AGGATGCGCA 1140
TCGCCAGTGC AGCCCGGGTC GTGGCCCCCC AACAGACCCA GTCCCGCCGC GACACGGCAG 1200
CAGCACCTCT TCGCCGCGAC ACGGCAGCAG CACCTCTTCG GCCCTTTGAG CTCTTCCCTC 1260
CTTATTTCTC AGTCTCATGC TACACTGCGA TTCTTTTATT TATTTGCTAT TTTAGGCAGT 1320
ATCCGCCGGC TCTCTACCAT GGACACTCAG TGAGGATTTG GTTCTCTTAG GTATGAACCC 1380
TGTGCTTCAC CTCCTGTGAG CTCCAAGACT CATTTCATCA GTTTTGGGAT GCATCAGTAT 1440
TTGGTGTTTA CAGTATTATG GTTATGTAAA TATTGTTCCC AGCTGAGCTG TGCAGTACAT 1500
TGTGACAACA TTTTCCATTT TGTGTTGTTT GTTTTCCTGG GAATTCATAA TAGCCTGTTT 1560
TCTTCTTGCA TCAAGCTGGA 1580