EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-33476 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr17:21178360-21179870 
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF14MA0740.1chr17:21179211-21179225TGGGGGGCGTGGCT-6.26
KLF16MA0741.1chr17:21179213-21179224GGGGGCGTGGC-6.62
Klf12MA0742.1chr17:21179223-21179238CTGGAGGGCGTGGCC-6.16
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
GCTCTCAAGT CCCCATGCAC AAAAAATAAC CTGCAGACTC AGGACTGTGT AAATCTATCC 60
TCAGGAGGGC AAAGAAAGCC ACTTCTCTAA GCACGCCGGG GGCATACTGG CTGCCCGCCC 120
AACAGATGTC TGGATCAGTC TGAATCCTGG GCACCCGGGA GAGGAAATGA ATTCCCTTCA 180
TCAGCGGCCT CGAGCCCCCA GCAGTCCTCC TCCACCCGGG GACAAATTCT TCTCTCCCCC 240
CAAGAATGTT TGCAATCCTT CGGATGGCAG TTTTCCAAGA CCGACCACTT GAATGTCCTC 300
TCTACCCTCA TAAAAGCAAG ACCTGTTCCT TGCTGGGAAA GCATGGGGTG GGTGATCGTC 360
TTCAACCTTT AAAGGGCTGG ACCCGTAGCT GCTGCACCCG GGGGCACAGC TGACGGGAGA 420
GGAGAAGCGG CCTCTTCTCA GCATGGGGAT GTGGGGAGCC GCTCAGGGAG AGAAAACGAG 480
GCCTTTACAG CACCGGTTTA ACAGCCTCGG CCACGCATCT GCCCGCACAG ATCTAAGGCT 540
TGGCTTCGGG TCCGGCTCCA CGCCTGCCCC ATGTCCCCAC GGTCCGCGGC CCTCGGGAGG 600
CCCGGCCCTG GGGGCTGAGC TCTGCCCTGG GACCGAAGGC CACTCTCCCA GCCAAGGCCG 660
GAGGGCTCTG CCCTGGGCAC ATGCGCCCCA TCCGCCTGCC CTGAGCTGAC CCCGCCGCTC 720
CACACCACCC CACTCGCGGC TGAAAAGCTG AAGGCAGCCG CACACTCGCC CTTGCAGCTT 780
GCCCTGCAGC CCGCGCGGCC ATGTGAGCAA GCGCAGCCAA TCAGAGGCTC GCCCTGGACT 840
CCGTCCCGGG CTGGGGGGCG TGGCTGGAGG GCGTGGCCGG GCGGTACCCG CGGCGTCTCT 900
GCGCTGCCGC CTTTGCTTGC GCGGCTGTGT AGGGGGTTGT GGCGGGCCGG AGAGTCCCCG 960
AGTGACTTAA CATTCTCTAA AAATACCCCA TTTTTGAACT TCGACGACCT GGGTTGGCCT 1020
GCTCACTCTG TGTCCCTGCG CTCCTCTGCT TCTCTGCTCC TTCGGTCTTG TGTGCTGGGG 1080
ACACGTGGGC CTTTCCAGTT CCCTGCAGCC ACCTTTGGTC TGTAGGAAGG CAGTGGCGCA 1140
GGGAGCGGTG GGAGCCCGGG TCTGCAGGGC TCAAGGTGGC GACGGCGAAG CGGTCTGCCC 1200
CACCCGCCAC CCCCACCCGC AGGATGCGCA TCGCCAGTGC AGCCCGGGTC GTGGCCCCCC 1260
AACAGACCCA GTCCCGCCGC GACACGGCAG CAGCACCTCT TCGCCGCGAC ACGGCAGCAG 1320
CACCTCTTCG GCCCTTTGAG CTCTTCCCTC CTTATTTCTC AGTCTCATGC TACACTGCGA 1380
TTCTTTTATT TATTTGCTAT TTTAGGCAGT ATCCGCCGGC TCTCTACCAT GGACACTCAG 1440
TGAGGATTTG GTTCTCTTAG GTATGAACCC TGTGCTTCAC CTCCTGTGAG CTCCAAGACT 1500
CATTTCATCA 1510