EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-23564 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr17:21177840-21179760 
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: 1             
ChromosomeStartEnd
chr172117910021179414
Number: 1             
IDChromosomeStartEnd
GH17I021274chr172117825321180112
Enhancer Sequence
AGAAGGGAGA GATCCCATCA CCAGCAGAAA TGCCCATGTT TGGGCCATGT GGCCTCCAAG 60
GAGGGTGCCA ATTCAGTGCC CTCCATTCCC AGACAGGACT ACTCAGGATC CCCAGTCCAA 120
GGCTGCTCCT TCTCTGCCCT GCACCGACTG CCGCAGGGGT TCTCACAGCC TTTCCTCCTG 180
CCTCAAGCCA TTCACATCAC TTGGGCAAGG TGGACTCTGC AACCTCCGCC TCTCGGATTC 240
AAGCGTTTCT CCTGCCTCAG CCTCCCGAGT AGCTGGGAGT ACAGACACAC GCCACCACGC 300
CCGGCTAATT TTTTTGTATT TTTAGTAGAG ACTAAAAAAA CCATGGGTTT TGCCATGTTG 360
GCCAGGCTGG TCTCAAACTT CTGACCTCAG GTGATCCGCC TGCCTCAGCC TCCCAAAGTC 420
CTGGGATTAC AGGTGTGAGC CACCATGCCC CGCCGACTTG CTCTGTTGTA GAGGGGCAGC 480
CTTGAAGACG GTGCATCCTT CTTGCTGCAG ACTATTCTTG GCTCTCAAGT CCCCATGCAC 540
AAAAAATAAC CTGCAGACTC AGGACTGTGT AAATCTATCC TCAGGAGGGC AAAGAAAGCC 600
ACTTCTCTAA GCACGCCGGG GGCATACTGG CTGCCCGCCC AACAGATGTC TGGATCAGTC 660
TGAATCCTGG GCACCCGGGA GAGGAAATGA ATTCCCTTCA TCAGCGGCCT CGAGCCCCCA 720
GCAGTCCTCC TCCACCCGGG GACAAATTCT TCTCTCCCCC CAAGAATGTT TGCAATCCTT 780
CGGATGGCAG TTTTCCAAGA CCGACCACTT GAATGTCCTC TCTACCCTCA TAAAAGCAAG 840
ACCTGTTCCT TGCTGGGAAA GCATGGGGTG GGTGATCGTC TTCAACCTTT AAAGGGCTGG 900
ACCCGTAGCT GCTGCACCCG GGGGCACAGC TGACGGGAGA GGAGAAGCGG CCTCTTCTCA 960
GCATGGGGAT GTGGGGAGCC GCTCAGGGAG AGAAAACGAG GCCTTTACAG CACCGGTTTA 1020
ACAGCCTCGG CCACGCATCT GCCCGCACAG ATCTAAGGCT TGGCTTCGGG TCCGGCTCCA 1080
CGCCTGCCCC ATGTCCCCAC GGTCCGCGGC CCTCGGGAGG CCCGGCCCTG GGGGCTGAGC 1140
TCTGCCCTGG GACCGAAGGC CACTCTCCCA GCCAAGGCCG GAGGGCTCTG CCCTGGGCAC 1200
ATGCGCCCCA TCCGCCTGCC CTGAGCTGAC CCCGCCGCTC CACACCACCC CACTCGCGGC 1260
TGAAAAGCTG AAGGCAGCCG CACACTCGCC CTTGCAGCTT GCCCTGCAGC CCGCGCGGCC 1320
ATGTGAGCAA GCGCAGCCAA TCAGAGGCTC GCCCTGGACT CCGTCCCGGG CTGGGGGGCG 1380
TGGCTGGAGG GCGTGGCCGG GCGGTACCCG CGGCGTCTCT GCGCTGCCGC CTTTGCTTGC 1440
GCGGCTGTGT AGGGGGTTGT GGCGGGCCGG AGAGTCCCCG AGTGACTTAA CATTCTCTAA 1500
AAATACCCCA TTTTTGAACT TCGACGACCT GGGTTGGCCT GCTCACTCTG TGTCCCTGCG 1560
CTCCTCTGCT TCTCTGCTCC TTCGGTCTTG TGTGCTGGGG ACACGTGGGC CTTTCCAGTT 1620
CCCTGCAGCC ACCTTTGGTC TGTAGGAAGG CAGTGGCGCA GGGAGCGGTG GGAGCCCGGG 1680
TCTGCAGGGC TCAAGGTGGC GACGGCGAAG CGGTCTGCCC CACCCGCCAC CCCCACCCGC 1740
AGGATGCGCA TCGCCAGTGC AGCCCGGGTC GTGGCCCCCC AACAGACCCA GTCCCGCCGC 1800
GACACGGCAG CAGCACCTCT TCGCCGCGAC ACGGCAGCAG CACCTCTTCG GCCCTTTGAG 1860
CTCTTCCCTC CTTATTTCTC AGTCTCATGC TACACTGCGA TTCTTTTATT TATTTGCTAT 1920