EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-34060 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr17:39948760-39951220 
TF binding sites/motifs
Number: 12             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr17:39950148-39950167CGACCAGCGGATGGCACCA+6.09
FOSL2MA0478.1chr17:39949567-39949578CTGAGTCACCC-6.02
JUNBMA0490.1chr17:39949567-39949578CTGAGTCACCC-6.02
NFAT5MA0606.1chr17:39951035-39951045AATGGAAAAT-6.02
NFATC1MA0624.1chr17:39951035-39951045AATGGAAAAT-6.02
NFATC3MA0625.1chr17:39951035-39951045AATGGAAAAT-6.02
TCFL5MA0632.2chr17:39949732-39949742TCACGCGCAC+6.02
ZEB1MA0103.3chr17:39949631-39949642CCCACCTGCCC+6.14
ZNF263MA0528.1chr17:39949364-39949385GGTGGAGGGAGAGGCTGGAGG+6.14
ZNF263MA0528.1chr17:39950879-39950900TGCCCCTTCCCAGCCTCCTCC-6.26
ZNF263MA0528.1chr17:39950882-39950903CCCTTCCCAGCCTCCTCCTCC-6.96
ZfxMA0146.2chr17:39948825-39948839CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 19             
IDCoordinateTissue/cell
SE_23177chr17:39948805-39950762Colon_Crypt_1
SE_23845chr17:39948823-39950568Colon_Crypt_2
SE_24826chr17:39948792-39950552Colon_Crypt_3
SE_26576chr17:39947886-39951114Esophagus
SE_27684chr17:39947694-39953126Fetal_Intestine
SE_28604chr17:39947659-39953352Fetal_Intestine_Large
SE_31640chr17:39948788-39951021Gastric
SE_35990chr17:39948033-39951096HMEC
SE_40900chr17:39947989-39951264Left_Ventricle
SE_42558chr17:39948749-39951297Lung
SE_47748chr17:39948821-39950630Pancreas
SE_48895chr17:39948755-39951241Right_Atrium
SE_49575chr17:39948820-39950509Right_Ventricle
SE_50269chr17:39948758-39951244Sigmoid_Colon
SE_52578chr17:39948765-39951219Small_Intestine
SE_56909chr17:39948805-39950751VACO_400
SE_57643chr17:39948796-39950605VACO_503
SE_58007chr17:39948820-39950619VACO_9m
SE_64699chr17:39948561-39950841NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr173994884139950945
chr173994911639949497
chr173994951739949745
Number: 1             
IDChromosomeStartEnd
GH17I041791chr173994788839953024
Enhancer Sequence
TAGTAGAGAT GGGGTTTCAC CATGTTGGCC AGGCTGGTCT TGAACTCCTG ACCCCAAGTG 60
ATCCACCCGC CTCGGCCTCC CAAAGTGCTG GGATTACAGG TGTGAGTCAC CACAACTGGC 120
CTGGGAGTGT GCTCTGTAAC TTACCTAGAT CTATGGCATG TAGGCCTCAT TTGTGCTCTT 180
GGCCCTGCCC ACTGGCTTTG GGGGTGGGGG CTTACTCAGA AGGCCCCCTT CAGGGCTCGG 240
GGAGGACACA GCTGCAGAAG AGCCTGCAGG CTCCCAAACT CTGCTGGCTG GAGTGGGCCC 300
AAGCATGGCC AGAAGCTGGG AAGGGAGCAG GAGGCTGCAG GGCTCTGGAG GGAGGCTGTG 360
GGGAGATGGA CTCCTGCCTT TTTTCCTGCC TTGTGTCCAG GGGAGGGGCC TTGAGGCCAG 420
AGGCTGCCCA CAGCCTGGTC CTGTGGGCGT GTGTCTTTTA ATTACAGATG TAGCTCCAGC 480
GACACTTCAC TGCAAGGCGT GTGGGTGGGG ATGGAATGTC AGAAGGAAAA CAGGAGACAA 540
GAAAACAGAG ATAGGACGGG CCAGAAATAG TACAGGCCAG GGTGAGATAG CAGCGGCCAG 600
TGGTGGTGGA GGGAGAGGCT GGAGGAGGGT CTGTCGAAAC CTCTCCAGAG AATGCCTGTC 660
CCAGGCTGCC CCTCCTTATT CACCCCAAGC CCCGCAAGTT GAAACTCCAG GACCGGTGGC 720
ATCTAGATCG GGCTCCAGAG CTGGTTCACC AACTCCCTAA GCAACACCCT CCTCCTGAGT 780
GGGGAGGGGT AGCCGAGCCT TTGCGACCTG AGTCACCCGC TTCCTGCTCC TGGTCTGGGC 840
GACTCCATGC ACAGGCTGAC ACAGCTGGGG CCCCACCTGC CCTGCCAGCC TGTCCCGCTC 900
CTCCCTCTTT CCACAAGCCA GGAGAGATGC CTGCCCTGAC AAGGCATGCT TCCCACGGAG 960
AGGCCATCCC TCTCACGCGC ACACACGGCT GGAGGCAGCC ATTTCTCCCT GACCTGTGGA 1020
GAGCCTTGGG AAGAGGAAGA AGGCATAGTC TAAGCGGAGC CCCCTTTTCC CTGCATCTAT 1080
GAAGAAACTG CGGCTGGAGC CAGGAGAGGG ACTTCCCCAA GATCACACAA GAAAATTCCT 1140
GGCAGGGCTG GGACTTGAAC CTTGGTCTTC TGCCAGCCAG TTCACCTCCC CCACCAATGT 1200
AGGTCTCTTT CCACCCCAAG GAAGGCAAAG ACGGGCTGCA GTCAGGGAGG AGACGAGAAC 1260
CAATTTTGCC AGCTTGATTT TGTCAGCTCA GAGGTGTGAC CCCAGGAAAA CCTTGGAGTT 1320
AGACAGCCAG GGCTGGGGGA GGGGGTGGCT CTGGGTGGTC CCAGACTCAG GCCTTACTTC 1380
CCCTAAGCCG ACCAGCGGAT GGCACCACCT AGAGCCTCTA GCCATCAATT ATGCAAACAG 1440
ACCCTTCCCC ACCCCCGCCT CTCGCCCTCC GGCCCTCTCT GCTTCCCAGG TCTTTAAGCG 1500
CTGGACTCCA CCTGGCTGAG AACTGGGACA GGACTCAGCG GCCCCTGGCC TTGTACTTTC 1560
ATCCCATCTT TCCCAGTCCC ATCCCACGGC CCCCAGGGAA TTTGAGAGTT GAGATCCTTG 1620
AATATTTCAT CAGCACTTCA GCCTCCAGTG GAAGCAGCAG CCAACTTACA TCTCCTGGAG 1680
CATTTATGGC CCCAACAGAG AACCTGGAAG TAGCCAGGGG GAGGGGTGGG TGCATGGGGG 1740
AGGGTGAAGC TTGGGCCAGG CTGCCAATAA GGGTTGATGG AGAAGAAGGC TGCCGGGTCC 1800
AAAGTGTGTG TGAGCTGGGG GAAAGGGGCT CCAAAGCCGG GAACATTTCC GTGTTTGAGG 1860
ATACAGATGT ATTTTAAAAT AAATAAACAA AATGGAGTTA TCAAAACAAT TATACGCAAG 1920
GTTAAAGTCA TATGACAGGG TTTTCTGACT TCAGTCCTGC CCCTGTCTCG TGACTGGGTT 1980
TATAACCTCA TCCGGAGATA AGGTAAAAAA TTTTAATGGG AGCTTTTTTT TTTTTAGGGC 2040
TGTGAGGCCC TCAAATGACC CCCTACTGCC TGGGGCCAGG GAGGAAAGGC CAAATTCTCC 2100
AGCTACATTG GCTGAAACTT GCCCCTTCCC AGCCTCCTCC TCCAGGAAGG TCAGGAGGAT 2160
TTAGCCCAGT AGTCAAGGAA AAATAAAGTA ATTTGGCTTA GCTACCCCTT ATTTTACCCC 2220
AGAAACACAA TATCACACTT TTCTTCTGAA AAGAAAGGTG AAAAGGGTGA CCTCAAATGG 2280
AAAATGTCAA GTTCTCTTGG CCTCTTCTTT GCACATGACC TCACTTAGTA AGTTCTTCTG 2340
GAGAGCGAAA GGATCAAGGC TGAGCGAGGT GGCTCACGCC TGTAATCCCA GCACTTTGTG 2400
AGGCCGAGGT GGGCAGATCA CCTGAGGTAG AGAGCTCGAG ACTAGCCTGA CCAACATGGA 2460