EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS076-24183 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr17:21178440-21180150 
TF binding sites/motifs
Number: 14             
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
ZEB1MA0103.3chr17:21180134-21180145CCCACCTGCCC+6.14
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
ACTTCTCTAA GCACGCCGGG GGCATACTGG CTGCCCGCCC AACAGATGTC TGGATCAGTC 60
TGAATCCTGG GCACCCGGGA GAGGAAATGA ATTCCCTTCA TCAGCGGCCT CGAGCCCCCA 120
GCAGTCCTCC TCCACCCGGG GACAAATTCT TCTCTCCCCC CAAGAATGTT TGCAATCCTT 180
CGGATGGCAG TTTTCCAAGA CCGACCACTT GAATGTCCTC TCTACCCTCA TAAAAGCAAG 240
ACCTGTTCCT TGCTGGGAAA GCATGGGGTG GGTGATCGTC TTCAACCTTT AAAGGGCTGG 300
ACCCGTAGCT GCTGCACCCG GGGGCACAGC TGACGGGAGA GGAGAAGCGG CCTCTTCTCA 360
GCATGGGGAT GTGGGGAGCC GCTCAGGGAG AGAAAACGAG GCCTTTACAG CACCGGTTTA 420
ACAGCCTCGG CCACGCATCT GCCCGCACAG ATCTAAGGCT TGGCTTCGGG TCCGGCTCCA 480
CGCCTGCCCC ATGTCCCCAC GGTCCGCGGC CCTCGGGAGG CCCGGCCCTG GGGGCTGAGC 540
TCTGCCCTGG GACCGAAGGC CACTCTCCCA GCCAAGGCCG GAGGGCTCTG CCCTGGGCAC 600
ATGCGCCCCA TCCGCCTGCC CTGAGCTGAC CCCGCCGCTC CACACCACCC CACTCGCGGC 660
TGAAAAGCTG AAGGCAGCCG CACACTCGCC CTTGCAGCTT GCCCTGCAGC CCGCGCGGCC 720
ATGTGAGCAA GCGCAGCCAA TCAGAGGCTC GCCCTGGACT CCGTCCCGGG CTGGGGGGCG 780
TGGCTGGAGG GCGTGGCCGG GCGGTACCCG CGGCGTCTCT GCGCTGCCGC CTTTGCTTGC 840
GCGGCTGTGT AGGGGGTTGT GGCGGGCCGG AGAGTCCCCG AGTGACTTAA CATTCTCTAA 900
AAATACCCCA TTTTTGAACT TCGACGACCT GGGTTGGCCT GCTCACTCTG TGTCCCTGCG 960
CTCCTCTGCT TCTCTGCTCC TTCGGTCTTG TGTGCTGGGG ACACGTGGGC CTTTCCAGTT 1020
CCCTGCAGCC ACCTTTGGTC TGTAGGAAGG CAGTGGCGCA GGGAGCGGTG GGAGCCCGGG 1080
TCTGCAGGGC TCAAGGTGGC GACGGCGAAG CGGTCTGCCC CACCCGCCAC CCCCACCCGC 1140
AGGATGCGCA TCGCCAGTGC AGCCCGGGTC GTGGCCCCCC AACAGACCCA GTCCCGCCGC 1200
GACACGGCAG CAGCACCTCT TCGCCGCGAC ACGGCAGCAG CACCTCTTCG GCCCTTTGAG 1260
CTCTTCCCTC CTTATTTCTC AGTCTCATGC TACACTGCGA TTCTTTTATT TATTTGCTAT 1320
TTTAGGCAGT ATCCGCCGGC TCTCTACCAT GGACACTCAG TGAGGATTTG GTTCTCTTAG 1380
GTATGAACCC TGTGCTTCAC CTCCTGTGAG CTCCAAGACT CATTTCATCA GTTTTGGGAT 1440
GCATCAGTAT TTGGTGTTTA CAGTATTATG GTTATGTAAA TATTGTTCCC AGCTGAGCTG 1500
TGCAGTACAT TGTGACAACA TTTTCCATTT TGTGTTGTTT GTTTTCCTGG GAATTCATAA 1560
TAGCCTGTTT TCTTCTTGCA TCAAGCTGGA CACTCAGTGG ATCCTTTCAA ATCTGGAGAC 1620
ATGACCTTCG GTTCTGGGAA GCTGGAAGGC ACAAGTGCTG TTTTTACAAG CTCTGAACTC 1680
ATCTTGTTTC TGTCCCCACC TGCCCCCCCA 1710