EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS007-00148 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr1:16501660-16503430 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6BMA0731.1chr1:16503374-16503391TGCTTCCTAGGAAGTGA+6.08
RREB1MA0073.1chr1:16502026-16502046TGTGAGGGGGTGGGAGGGGG-6.61
RREB1MA0073.1chr1:16502036-16502056TGGGAGGGGGTGGGATGGGG-7.16
SOX10MA0442.2chr1:16502839-16502850TTCTTTGTTTT-6.62
ZNF263MA0528.1chr1:16503057-16503078CATCCTCCTCCATCCTCCTCC-6.3
ZNF263MA0528.1chr1:16503060-16503081CCTCCTCCATCCTCCTCCTCC-8.07
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_23091chr1:16501962-16502745Colon_Crypt_1
SE_23091chr1:16502844-16503560Colon_Crypt_1
SE_23751chr1:16502050-16502674Colon_Crypt_2
SE_23751chr1:16502855-16503434Colon_Crypt_2
SE_24743chr1:16497841-16502803Colon_Crypt_3
SE_24743chr1:16502816-16503501Colon_Crypt_3
SE_26540chr1:16496436-16504779Esophagus
SE_28102chr1:16497879-16504574Fetal_Intestine
SE_29455chr1:16497964-16506131Fetal_Intestine_Large
SE_31527chr1:16499336-16504399Gastric
SE_34268chr1:16497740-16504248HCT-116
SE_34628chr1:16497415-16506115HeLa
SE_36144chr1:16502024-16503485HMEC
SE_38062chr1:16499064-16503878HUVEC
SE_40833chr1:16501759-16503971Left_Ventricle
SE_44998chr1:16502053-16503662NHLF
SE_46140chr1:16501795-16503844Osteoblasts
SE_47009chr1:16502010-16502676Ovary
SE_47009chr1:16502860-16503560Ovary
SE_47150chr1:16499250-16512083Panc1
SE_47539chr1:16501964-16502662Pancreas
SE_47539chr1:16502819-16503601Pancreas
SE_48744chr1:16501448-16503785Right_Atrium
SE_50427chr1:16497958-16504232Sigmoid_Colon
SE_52536chr1:16501918-16504326Small_Intestine
SE_56795chr1:16499345-16504738VACO_400
SE_57357chr1:16501943-16502709VACO_503
SE_57939chr1:16501961-16502682VACO_9m
SE_57939chr1:16502843-16503425VACO_9m
SE_64726chr1:16502266-16503212NHEK
SE_65472chr1:16498579-16501949Pancreatic_islets
SE_65472chr1:16501980-16503977Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11650207416503312
Number: 1             
IDChromosomeStartEnd
GH01I016171chr11649794116511884
Enhancer Sequence
GTGGGCCGCA CTCCCTCCAT GGGCCCTGGG GTGCCGGGGC TGGCCCCATA CCCCAGAAGC 60
TCCCCACTAC CTCCGGGTGT GGAGCTATGG TGGGCGAGCA AACCTGGGTT CAGATCCCAC 120
CTTCTACTCA TCATGAGACT TGGGCAAGTG TTTTAAGCCC TCGGAGCCTC AGTTTCATGA 180
TCTGTAAAGT GGACATTAGA GTCGCTCGGG ATGCGGGATG CTTGAATGAG ATGATGCACT 240
CAGCACGCGG CAGGCCCTGG GGCCCTGTGT GCTCTACAAT TGCAGCTGCT ATTAGACCAG 300
CTTCTTTCTT GCCTGGGTAT GTGGGGCTTA GGCCAGAACA AATCTTGGGA CTGAGTGTAA 360
AATATATGTG AGGGGGTGGG AGGGGGTGGG ATGGGGCTCG GTGCGGGCCT GGCAGGTGTG 420
CTGGGAGGCA AGGCCTATGA CTCCTGTGGG CCTGCTCTTC CTCCCATCCC ACCCTCCACA 480
GTCCCCACCT CAGGGGCCCT GGGCCTGGGG CAGCAGGGGC CGGGATGTGT CTCTCCAGAG 540
CAGGAACGGA GGGGCCTCCG CAACTGGTTG GGGAGGGGGG GTGGATGCCA GCCCCCGCTG 600
ATTAGGTCTC AAATTAAAGC CGAGCTTGCT CCTGTCGCTG CTCAGGCAGG CCCTCCTCCT 660
GGCCACAGTT CCCTGCCTGG CCCTCTGCTT CGGGCCTCAT GGTGGCTGGT TGCTCCCAGC 720
CTAGAATTGC TAAAAGGCTC CCGTAGTGGG TAGGAGCCTC AGGGGACCTG GGAGAGGCTT 780
CAGGGGCCCT GCCTGTGCGG GGGTCTCTCC TGTGACCCTC AGACCTGAGC CAGTGTCTGG 840
GGACAAGTCA CCGTGTCAGA GGCTGCGGAG AGCAAAGCCC AGGCGGTGAT GACTTGAGTT 900
TCCAGGCCGG GTGCCAGGAG GCCCGCGGTC ACACTCCGCC TGGGGCCTGG GCTCCGGCCA 960
ACTGTCAGCA GCAGAGATTG TTGGGTTGGT TTTATTTTAA ACAAAAAAGA ACTTTGAGTG 1020
GAAACATGTG TTTCTTTTTT CTCCCCCTTC CCTCTCTCCC TATCTCTCTC CATCTCATCA 1080
TGGAATATTT CTCTTTTTTG TACCTCCCTT TCTCTGTTTT TCTCTCTGTC TTCCTCTATT 1140
TGTCCCTGCC TCTGTCTCTC TCTCTCTCTC TCTCATTCTT TCTTTGTTTT CCTATCTCTT 1200
GATTTCTCTG TCTCTTTCTC TATTTCTTTT TCCGCAGCTT TCAGGAGTCA GGAGAGGTAC 1260
CAGACTTCCT CCCTCGGGGT GTGGCCTGGG CCCCTGCCAT AAAATCCCCA GGCGTGCCAC 1320
GGCCCTATGT CGGGGGTCTG CCGCTCCAGG GGAGGGAGGG GGTGTCTAGC AGCGGAGGCT 1380
CCAGGACCCA AATGCTCCAT CCTCCTCCAT CCTCCTCCTC CAAGCTCCCA CTGCCCCTGC 1440
ATCTGCCCTT CCTGTGTCTG TTTTCTCTAC TAAGCATCTA GAAAATAATT CTGCAGCTTG 1500
AGACAAGTTT TAAAACACTG GTCTGGCCCA AACCACCCAT CTACAGCCAG AGACTGGCGC 1560
CGAGGAGGGG ACCATGGCCT GCTCAACACC GCACGGAGGG TTAGGGGCAA AGCCAGGCCG 1620
ACCCAGGTCC CCCACTCCCA AGTGACATTA CTGACACCCC CAAACCCACA GTCACCACAC 1680
TTCTCAGGTC CCTGCGTCTT TCAGAGGGGT GGTCTGCTTC CTAGGAAGTG ATGTGCCCTC 1740
CCCTAAGGTG GTCACCCAGC ACAAGGGTCC 1770