EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS059-19139 
Organism
Homo sapiens 
Tissue/cell
GM12878 
Coordinate
chr17:21178400-21180110 
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
AGGACTGTGT AAATCTATCC TCAGGAGGGC AAAGAAAGCC ACTTCTCTAA GCACGCCGGG 60
GGCATACTGG CTGCCCGCCC AACAGATGTC TGGATCAGTC TGAATCCTGG GCACCCGGGA 120
GAGGAAATGA ATTCCCTTCA TCAGCGGCCT CGAGCCCCCA GCAGTCCTCC TCCACCCGGG 180
GACAAATTCT TCTCTCCCCC CAAGAATGTT TGCAATCCTT CGGATGGCAG TTTTCCAAGA 240
CCGACCACTT GAATGTCCTC TCTACCCTCA TAAAAGCAAG ACCTGTTCCT TGCTGGGAAA 300
GCATGGGGTG GGTGATCGTC TTCAACCTTT AAAGGGCTGG ACCCGTAGCT GCTGCACCCG 360
GGGGCACAGC TGACGGGAGA GGAGAAGCGG CCTCTTCTCA GCATGGGGAT GTGGGGAGCC 420
GCTCAGGGAG AGAAAACGAG GCCTTTACAG CACCGGTTTA ACAGCCTCGG CCACGCATCT 480
GCCCGCACAG ATCTAAGGCT TGGCTTCGGG TCCGGCTCCA CGCCTGCCCC ATGTCCCCAC 540
GGTCCGCGGC CCTCGGGAGG CCCGGCCCTG GGGGCTGAGC TCTGCCCTGG GACCGAAGGC 600
CACTCTCCCA GCCAAGGCCG GAGGGCTCTG CCCTGGGCAC ATGCGCCCCA TCCGCCTGCC 660
CTGAGCTGAC CCCGCCGCTC CACACCACCC CACTCGCGGC TGAAAAGCTG AAGGCAGCCG 720
CACACTCGCC CTTGCAGCTT GCCCTGCAGC CCGCGCGGCC ATGTGAGCAA GCGCAGCCAA 780
TCAGAGGCTC GCCCTGGACT CCGTCCCGGG CTGGGGGGCG TGGCTGGAGG GCGTGGCCGG 840
GCGGTACCCG CGGCGTCTCT GCGCTGCCGC CTTTGCTTGC GCGGCTGTGT AGGGGGTTGT 900
GGCGGGCCGG AGAGTCCCCG AGTGACTTAA CATTCTCTAA AAATACCCCA TTTTTGAACT 960
TCGACGACCT GGGTTGGCCT GCTCACTCTG TGTCCCTGCG CTCCTCTGCT TCTCTGCTCC 1020
TTCGGTCTTG TGTGCTGGGG ACACGTGGGC CTTTCCAGTT CCCTGCAGCC ACCTTTGGTC 1080
TGTAGGAAGG CAGTGGCGCA GGGAGCGGTG GGAGCCCGGG TCTGCAGGGC TCAAGGTGGC 1140
GACGGCGAAG CGGTCTGCCC CACCCGCCAC CCCCACCCGC AGGATGCGCA TCGCCAGTGC 1200
AGCCCGGGTC GTGGCCCCCC AACAGACCCA GTCCCGCCGC GACACGGCAG CAGCACCTCT 1260
TCGCCGCGAC ACGGCAGCAG CACCTCTTCG GCCCTTTGAG CTCTTCCCTC CTTATTTCTC 1320
AGTCTCATGC TACACTGCGA TTCTTTTATT TATTTGCTAT TTTAGGCAGT ATCCGCCGGC 1380
TCTCTACCAT GGACACTCAG TGAGGATTTG GTTCTCTTAG GTATGAACCC TGTGCTTCAC 1440
CTCCTGTGAG CTCCAAGACT CATTTCATCA GTTTTGGGAT GCATCAGTAT TTGGTGTTTA 1500
CAGTATTATG GTTATGTAAA TATTGTTCCC AGCTGAGCTG TGCAGTACAT TGTGACAACA 1560
TTTTCCATTT TGTGTTGTTT GTTTTCCTGG GAATTCATAA TAGCCTGTTT TCTTCTTGCA 1620
TCAAGCTGGA CACTCAGTGG ATCCTTTCAA ATCTGGAGAC ATGACCTTCG GTTCTGGGAA 1680
GCTGGAAGGC ACAAGTGCTG TTTTTACAAG 1710