EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS049-03238 
Organism
Homo sapiens 
Tissue/cell
Fetal_spinal_cord 
Coordinate
chr17:21177870-21179830 
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
TGCCCATGTT TGGGCCATGT GGCCTCCAAG GAGGGTGCCA ATTCAGTGCC CTCCATTCCC 60
AGACAGGACT ACTCAGGATC CCCAGTCCAA GGCTGCTCCT TCTCTGCCCT GCACCGACTG 120
CCGCAGGGGT TCTCACAGCC TTTCCTCCTG CCTCAAGCCA TTCACATCAC TTGGGCAAGG 180
TGGACTCTGC AACCTCCGCC TCTCGGATTC AAGCGTTTCT CCTGCCTCAG CCTCCCGAGT 240
AGCTGGGAGT ACAGACACAC GCCACCACGC CCGGCTAATT TTTTTGTATT TTTAGTAGAG 300
ACTAAAAAAA CCATGGGTTT TGCCATGTTG GCCAGGCTGG TCTCAAACTT CTGACCTCAG 360
GTGATCCGCC TGCCTCAGCC TCCCAAAGTC CTGGGATTAC AGGTGTGAGC CACCATGCCC 420
CGCCGACTTG CTCTGTTGTA GAGGGGCAGC CTTGAAGACG GTGCATCCTT CTTGCTGCAG 480
ACTATTCTTG GCTCTCAAGT CCCCATGCAC AAAAAATAAC CTGCAGACTC AGGACTGTGT 540
AAATCTATCC TCAGGAGGGC AAAGAAAGCC ACTTCTCTAA GCACGCCGGG GGCATACTGG 600
CTGCCCGCCC AACAGATGTC TGGATCAGTC TGAATCCTGG GCACCCGGGA GAGGAAATGA 660
ATTCCCTTCA TCAGCGGCCT CGAGCCCCCA GCAGTCCTCC TCCACCCGGG GACAAATTCT 720
TCTCTCCCCC CAAGAATGTT TGCAATCCTT CGGATGGCAG TTTTCCAAGA CCGACCACTT 780
GAATGTCCTC TCTACCCTCA TAAAAGCAAG ACCTGTTCCT TGCTGGGAAA GCATGGGGTG 840
GGTGATCGTC TTCAACCTTT AAAGGGCTGG ACCCGTAGCT GCTGCACCCG GGGGCACAGC 900
TGACGGGAGA GGAGAAGCGG CCTCTTCTCA GCATGGGGAT GTGGGGAGCC GCTCAGGGAG 960
AGAAAACGAG GCCTTTACAG CACCGGTTTA ACAGCCTCGG CCACGCATCT GCCCGCACAG 1020
ATCTAAGGCT TGGCTTCGGG TCCGGCTCCA CGCCTGCCCC ATGTCCCCAC GGTCCGCGGC 1080
CCTCGGGAGG CCCGGCCCTG GGGGCTGAGC TCTGCCCTGG GACCGAAGGC CACTCTCCCA 1140
GCCAAGGCCG GAGGGCTCTG CCCTGGGCAC ATGCGCCCCA TCCGCCTGCC CTGAGCTGAC 1200
CCCGCCGCTC CACACCACCC CACTCGCGGC TGAAAAGCTG AAGGCAGCCG CACACTCGCC 1260
CTTGCAGCTT GCCCTGCAGC CCGCGCGGCC ATGTGAGCAA GCGCAGCCAA TCAGAGGCTC 1320
GCCCTGGACT CCGTCCCGGG CTGGGGGGCG TGGCTGGAGG GCGTGGCCGG GCGGTACCCG 1380
CGGCGTCTCT GCGCTGCCGC CTTTGCTTGC GCGGCTGTGT AGGGGGTTGT GGCGGGCCGG 1440
AGAGTCCCCG AGTGACTTAA CATTCTCTAA AAATACCCCA TTTTTGAACT TCGACGACCT 1500
GGGTTGGCCT GCTCACTCTG TGTCCCTGCG CTCCTCTGCT TCTCTGCTCC TTCGGTCTTG 1560
TGTGCTGGGG ACACGTGGGC CTTTCCAGTT CCCTGCAGCC ACCTTTGGTC TGTAGGAAGG 1620
CAGTGGCGCA GGGAGCGGTG GGAGCCCGGG TCTGCAGGGC TCAAGGTGGC GACGGCGAAG 1680
CGGTCTGCCC CACCCGCCAC CCCCACCCGC AGGATGCGCA TCGCCAGTGC AGCCCGGGTC 1740
GTGGCCCCCC AACAGACCCA GTCCCGCCGC GACACGGCAG CAGCACCTCT TCGCCGCGAC 1800
ACGGCAGCAG CACCTCTTCG GCCCTTTGAG CTCTTCCCTC CTTATTTCTC AGTCTCATGC 1860
TACACTGCGA TTCTTTTATT TATTTGCTAT TTTAGGCAGT ATCCGCCGGC TCTCTACCAT 1920
GGACACTCAG TGAGGATTTG GTTCTCTTAG GTATGAACCC 1960