EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS002-00109 
Organism
Homo sapiens 
Tissue/cell
A375 
Coordinate
chr1:16501350-16504130 
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: 36             
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_47009chr1:16503623-16504003Ovary
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
CATATGCGTG CCCCCAGCTC TCAGCCCCTC ACTGCCTCCT TTAATCCCCA CAGATCTGCC 60
AGCCTTTGAT ACTCCTGTGG GTGGCCGAGC CGGGGTTCTG AATAGGAAGC TGAGGGCTCA 120
TGGGCTGCGG GGAAGCAGGC AGGGGCTGAG CCTGCCAGGC CTGCCCGAGG GAGGGGGCTG 180
TGGGCCCCTC GCCATTCACT GCTAAGCCTG GATCCGGGCG CCTTTGTGCC AAGAACAAAA 240
CCCGGGGGAT CAGCTGTTCT CAGGCCTGCC TCTCTCAGCT CCGGAAGGGA CGGAAGCCTG 300
GGCCTGAGGG GTGGGCCGCA CTCCCTCCAT GGGCCCTGGG GTGCCGGGGC TGGCCCCATA 360
CCCCAGAAGC TCCCCACTAC CTCCGGGTGT GGAGCTATGG TGGGCGAGCA AACCTGGGTT 420
CAGATCCCAC CTTCTACTCA TCATGAGACT TGGGCAAGTG TTTTAAGCCC TCGGAGCCTC 480
AGTTTCATGA TCTGTAAAGT GGACATTAGA GTCGCTCGGG ATGCGGGATG CTTGAATGAG 540
ATGATGCACT CAGCACGCGG CAGGCCCTGG GGCCCTGTGT GCTCTACAAT TGCAGCTGCT 600
ATTAGACCAG CTTCTTTCTT GCCTGGGTAT GTGGGGCTTA GGCCAGAACA AATCTTGGGA 660
CTGAGTGTAA AATATATGTG AGGGGGTGGG AGGGGGTGGG ATGGGGCTCG GTGCGGGCCT 720
GGCAGGTGTG CTGGGAGGCA AGGCCTATGA CTCCTGTGGG CCTGCTCTTC CTCCCATCCC 780
ACCCTCCACA GTCCCCACCT CAGGGGCCCT GGGCCTGGGG CAGCAGGGGC CGGGATGTGT 840
CTCTCCAGAG CAGGAACGGA GGGGCCTCCG CAACTGGTTG GGGAGGGGGG GTGGATGCCA 900
GCCCCCGCTG ATTAGGTCTC AAATTAAAGC CGAGCTTGCT CCTGTCGCTG CTCAGGCAGG 960
CCCTCCTCCT GGCCACAGTT CCCTGCCTGG CCCTCTGCTT CGGGCCTCAT GGTGGCTGGT 1020
TGCTCCCAGC CTAGAATTGC TAAAAGGCTC CCGTAGTGGG TAGGAGCCTC AGGGGACCTG 1080
GGAGAGGCTT CAGGGGCCCT GCCTGTGCGG GGGTCTCTCC TGTGACCCTC AGACCTGAGC 1140
CAGTGTCTGG GGACAAGTCA CCGTGTCAGA GGCTGCGGAG AGCAAAGCCC AGGCGGTGAT 1200
GACTTGAGTT TCCAGGCCGG GTGCCAGGAG GCCCGCGGTC ACACTCCGCC TGGGGCCTGG 1260
GCTCCGGCCA ACTGTCAGCA GCAGAGATTG TTGGGTTGGT TTTATTTTAA ACAAAAAAGA 1320
ACTTTGAGTG GAAACATGTG TTTCTTTTTT CTCCCCCTTC CCTCTCTCCC TATCTCTCTC 1380
CATCTCATCA TGGAATATTT CTCTTTTTTG TACCTCCCTT TCTCTGTTTT TCTCTCTGTC 1440
TTCCTCTATT TGTCCCTGCC TCTGTCTCTC TCTCTCTCTC TCTCATTCTT TCTTTGTTTT 1500
CCTATCTCTT GATTTCTCTG TCTCTTTCTC TATTTCTTTT TCCGCAGCTT TCAGGAGTCA 1560
GGAGAGGTAC CAGACTTCCT CCCTCGGGGT GTGGCCTGGG CCCCTGCCAT AAAATCCCCA 1620
GGCGTGCCAC GGCCCTATGT CGGGGGTCTG CCGCTCCAGG GGAGGGAGGG GGTGTCTAGC 1680
AGCGGAGGCT CCAGGACCCA AATGCTCCAT CCTCCTCCAT CCTCCTCCTC CAAGCTCCCA 1740
CTGCCCCTGC ATCTGCCCTT CCTGTGTCTG TTTTCTCTAC TAAGCATCTA GAAAATAATT 1800
CTGCAGCTTG AGACAAGTTT TAAAACACTG GTCTGGCCCA AACCACCCAT CTACAGCCAG 1860
AGACTGGCGC CGAGGAGGGG ACCATGGCCT GCTCAACACC GCACGGAGGG TTAGGGGCAA 1920
AGCCAGGCCG ACCCAGGTCC CCCACTCCCA AGTGACATTA CTGACACCCC CAAACCCACA 1980
GTCACCACAC TTCTCAGGTC CCTGCGTCTT TCAGAGGGGT GGTCTGCTTC CTAGGAAGTG 2040
ATGTGCCCTC CCCTAAGGTG GTCACCCAGC ACAAGGGTCC CCCTGGAAAA TGTCCTGCCT 2100
TGGCTGGTCA CCCCTCCCCC AGGACAGACA AGCTTTTGGG CCCCCACCTT TCAGCCCCTT 2160
CTGCCAGGCA GTAGAGAAGA GAGAAGAGAG ACTCGCAGGC ACAGTGGCTC ATGCCTGTAA 2220
TCCTAGCACT TTGGGAGGCC GAGGTGGGCA GATCACAAGG TCAGGAGATA CAGAAGAGAG 2280
ACTGGCCACC CATGCACTGG GCCCAGGTCC TAGCTCGACG TCTGAGTCCT TGTGTGACTG 2340
TGAATATGAC TTTTCCACTG GCTGGCCTCA GTTTCCCCAT CTTTGTAACA GAAGCCTTGC 2400
CTTTGCCGCG GATCCCCTCT CTGCTCTAAT ATGTTATGGT GTTCTCCTCT CCTTCCATGG 2460
AGAGGAATTC TGGAACATCA GACCAGGAGT GCCATCTCCT CTCCCAAAGT GAGAGGGACT 2520
GTCCTCAGTG TGGCCTCAAT AGGTCAACTC CCCTTCACTT CAGGTTCCTT GTCCCCTGTG 2580
TGCAAGGGCC CCAGATGCCA CCACCAAGGG GAGAGGTGCC ACCATGACCT GGTGCACCAT 2640
TGTCAAAGGT GCACTTTCTT GGGTGTCCGG GGTCATGCCA GGATTCATGC AGGGATAGGA 2700
GGGGCTGCCT GCGTGTCAGG GGCCCATTCC ACCCCTGTCT CCCACAGCCC CAGGAGTAAA 2760
GTCAGGGTAA GTGTGCGGGA 2780