EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS026-00348 
Organism
Homo sapiens 
Tissue/cell
CNCC 
Coordinate
chr1:16501340-16503750 
TF binding sites/motifs
Number: 7             
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
TFAP4MA0691.1chr1:16501598-16501608ATCAGCTGTT-6.02
ZNF263MA0528.1chr1:16503057-16503078CATCCTCCTCCATCCTCCTCC-6.3
ZNF263MA0528.1chr1:16503060-16503081CCTCCTCCATCCTCCTCCTCC-8.07
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_23091chr1:16499347-16501823Colon_Crypt_1
SE_23091chr1:16501962-16502745Colon_Crypt_1
SE_23091chr1:16502844-16503560Colon_Crypt_1
SE_23751chr1:16499364-16501671Colon_Crypt_2
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_47539chr1:16501350-16501756Pancreas
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
AGGGGAGTCA CATATGCGTG CCCCCAGCTC TCAGCCCCTC ACTGCCTCCT TTAATCCCCA 60
CAGATCTGCC AGCCTTTGAT ACTCCTGTGG GTGGCCGAGC CGGGGTTCTG AATAGGAAGC 120
TGAGGGCTCA TGGGCTGCGG GGAAGCAGGC AGGGGCTGAG CCTGCCAGGC CTGCCCGAGG 180
GAGGGGGCTG TGGGCCCCTC GCCATTCACT GCTAAGCCTG GATCCGGGCG CCTTTGTGCC 240
AAGAACAAAA CCCGGGGGAT CAGCTGTTCT CAGGCCTGCC TCTCTCAGCT CCGGAAGGGA 300
CGGAAGCCTG GGCCTGAGGG GTGGGCCGCA CTCCCTCCAT GGGCCCTGGG GTGCCGGGGC 360
TGGCCCCATA CCCCAGAAGC TCCCCACTAC CTCCGGGTGT GGAGCTATGG TGGGCGAGCA 420
AACCTGGGTT CAGATCCCAC CTTCTACTCA TCATGAGACT TGGGCAAGTG TTTTAAGCCC 480
TCGGAGCCTC AGTTTCATGA TCTGTAAAGT GGACATTAGA GTCGCTCGGG ATGCGGGATG 540
CTTGAATGAG ATGATGCACT CAGCACGCGG CAGGCCCTGG GGCCCTGTGT GCTCTACAAT 600
TGCAGCTGCT ATTAGACCAG CTTCTTTCTT GCCTGGGTAT GTGGGGCTTA GGCCAGAACA 660
AATCTTGGGA CTGAGTGTAA AATATATGTG AGGGGGTGGG AGGGGGTGGG ATGGGGCTCG 720
GTGCGGGCCT GGCAGGTGTG CTGGGAGGCA AGGCCTATGA CTCCTGTGGG CCTGCTCTTC 780
CTCCCATCCC ACCCTCCACA GTCCCCACCT CAGGGGCCCT GGGCCTGGGG CAGCAGGGGC 840
CGGGATGTGT CTCTCCAGAG CAGGAACGGA GGGGCCTCCG CAACTGGTTG GGGAGGGGGG 900
GTGGATGCCA GCCCCCGCTG ATTAGGTCTC AAATTAAAGC CGAGCTTGCT CCTGTCGCTG 960
CTCAGGCAGG CCCTCCTCCT GGCCACAGTT CCCTGCCTGG CCCTCTGCTT CGGGCCTCAT 1020
GGTGGCTGGT TGCTCCCAGC CTAGAATTGC TAAAAGGCTC CCGTAGTGGG TAGGAGCCTC 1080
AGGGGACCTG GGAGAGGCTT CAGGGGCCCT GCCTGTGCGG GGGTCTCTCC TGTGACCCTC 1140
AGACCTGAGC CAGTGTCTGG GGACAAGTCA CCGTGTCAGA GGCTGCGGAG AGCAAAGCCC 1200
AGGCGGTGAT GACTTGAGTT TCCAGGCCGG GTGCCAGGAG GCCCGCGGTC ACACTCCGCC 1260
TGGGGCCTGG GCTCCGGCCA ACTGTCAGCA GCAGAGATTG TTGGGTTGGT TTTATTTTAA 1320
ACAAAAAAGA ACTTTGAGTG GAAACATGTG TTTCTTTTTT CTCCCCCTTC CCTCTCTCCC 1380
TATCTCTCTC CATCTCATCA TGGAATATTT CTCTTTTTTG TACCTCCCTT TCTCTGTTTT 1440
TCTCTCTGTC TTCCTCTATT TGTCCCTGCC TCTGTCTCTC TCTCTCTCTC TCTCATTCTT 1500
TCTTTGTTTT CCTATCTCTT GATTTCTCTG TCTCTTTCTC TATTTCTTTT TCCGCAGCTT 1560
TCAGGAGTCA GGAGAGGTAC CAGACTTCCT CCCTCGGGGT GTGGCCTGGG CCCCTGCCAT 1620
AAAATCCCCA GGCGTGCCAC GGCCCTATGT CGGGGGTCTG CCGCTCCAGG GGAGGGAGGG 1680
GGTGTCTAGC AGCGGAGGCT CCAGGACCCA AATGCTCCAT CCTCCTCCAT CCTCCTCCTC 1740
CAAGCTCCCA CTGCCCCTGC ATCTGCCCTT CCTGTGTCTG TTTTCTCTAC TAAGCATCTA 1800
GAAAATAATT CTGCAGCTTG AGACAAGTTT TAAAACACTG GTCTGGCCCA AACCACCCAT 1860
CTACAGCCAG AGACTGGCGC CGAGGAGGGG ACCATGGCCT GCTCAACACC GCACGGAGGG 1920
TTAGGGGCAA AGCCAGGCCG ACCCAGGTCC CCCACTCCCA AGTGACATTA CTGACACCCC 1980
CAAACCCACA GTCACCACAC TTCTCAGGTC CCTGCGTCTT TCAGAGGGGT GGTCTGCTTC 2040
CTAGGAAGTG ATGTGCCCTC CCCTAAGGTG GTCACCCAGC ACAAGGGTCC CCCTGGAAAA 2100
TGTCCTGCCT TGGCTGGTCA CCCCTCCCCC AGGACAGACA AGCTTTTGGG CCCCCACCTT 2160
TCAGCCCCTT CTGCCAGGCA GTAGAGAAGA GAGAAGAGAG ACTCGCAGGC ACAGTGGCTC 2220
ATGCCTGTAA TCCTAGCACT TTGGGAGGCC GAGGTGGGCA GATCACAAGG TCAGGAGATA 2280
CAGAAGAGAG ACTGGCCACC CATGCACTGG GCCCAGGTCC TAGCTCGACG TCTGAGTCCT 2340
TGTGTGACTG TGAATATGAC TTTTCCACTG GCTGGCCTCA GTTTCCCCAT CTTTGTAACA 2400
GAAGCCTTGC 2410