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

TagContent
EnhancerAtlas ID
HS104-00557 
Organism
Homo sapiens 
Tissue/cell
HUVEC 
Coordinate
chr1:16498650-16500970 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MAFFMA0495.3chr1:16500147-16500162CTGCTGACTCAGCGC-7.07
MAFFMA0495.3chr1:16500147-16500162CTGCTGACTCAGCGC+7
RREB1MA0073.1chr1:16498769-16498789CCCCCTCCCACCCCACCCCA+6.5
Spz1MA0111.1chr1:16499568-16499579AGGGTATCAGC+6.32
ZEB1MA0103.3chr1:16500289-16500300GGGCAGGTGGG-6.14
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_23091chr1:16497584-16499266Colon_Crypt_1
SE_23091chr1:16499347-16501823Colon_Crypt_1
SE_23751chr1:16497995-16499231Colon_Crypt_2
SE_23751chr1:16499364-16501671Colon_Crypt_2
SE_24743chr1:16497841-16502803Colon_Crypt_3
SE_26540chr1:16496436-16504779Esophagus
SE_28102chr1:16497879-16504574Fetal_Intestine
SE_29455chr1:16497964-16506131Fetal_Intestine_Large
SE_31527chr1:16497806-16499321Gastric
SE_31527chr1:16499336-16504399Gastric
SE_34268chr1:16497740-16504248HCT-116
SE_34628chr1:16497415-16506115HeLa
SE_36144chr1:16498765-16501519HMEC
SE_38062chr1:16499064-16503878HUVEC
SE_44998chr1:16499693-16500212NHLF
SE_46140chr1:16499323-16500582Osteoblasts
SE_47150chr1:16497663-16499232Panc1
SE_47150chr1:16499250-16512083Panc1
SE_47539chr1:16499523-16500148Pancreas
SE_47539chr1:16500355-16501118Pancreas
SE_50427chr1:16497958-16504232Sigmoid_Colon
SE_52536chr1:16497970-16501408Small_Intestine
SE_56795chr1:16496450-16499306VACO_400
SE_56795chr1:16499345-16504738VACO_400
SE_57357chr1:16499350-16500174VACO_503
SE_57357chr1:16500236-16501136VACO_503
SE_57939chr1:16499369-16500862VACO_9m
SE_64726chr1:16499137-16501292NHEK
SE_65472chr1:16498579-16501949Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr11649960716500371
chr11649976116499895
Number: 1             
IDChromosomeStartEnd
GH01I016171chr11649794116511884
Enhancer Sequence
TCTCCCCCAC TGTAAACCTG CAAGGGCAGC CACGGCCGGG AGCAGCTGGT CCTGAGACTT 60
GGGCAGAGGC CCTGGACAGT GGGGCAGAAG CGCTTGGCTG GCCAGGAATT GGATCACTGC 120
CCCCTCCCAC CCCACCCCAT TCAGCCCTGT CTCCCACGGA CTCTGACCAC CCCTTGGTTC 180
TCTTATCAAA AACCGCCAAA ACCCGCCATC GAAACTCCCA GCCTCCTGAC CCCCATGCCC 240
CACCCGGCTC CACCCGTCTT CCCAACCTGG CATCCAGTGC CCCAAACCTG CCTATTCCGT 300
TCCTGGGAAG ACCCAGAAGG GAGCAGAGCT GGCACCAGGA GGCCAACAAC CCAGGCCCCC 360
TCCGTCCCTA GCCCCTCCTG GCCCTGGGCC CTCCACCCTA CTGTTTCTCC TGGGGTGTGC 420
CTTTCTTTGC CTTATGCCTC GGCATCTCTA AGTGGCAGGG GATGGAGTGG AGTGAGGGCG 480
GCAGGCCAAG GGCATGGCCC ATAATGAAAA AGGAATCTGG TTGGGCATGG TGGCTCACCC 540
TTGTAATCTC AGCACTTTGG GAGGCCAAGG CAGGCAGATC ATGAGGTCAG GAGATCGAGA 600
GCAGCCTAGC CAACATGGTG AAACCCCGTC TCTACTAAAA ACACAAAAAT TAGCTGGACG 660
TGGTGGTGGG CGCCTGTAAT CCCAGCTACT CGGGAGGCTG AGGCAGGAGA ATTGCTGGAA 720
CCCGGGAGGT GGAGGTTGCA GTGAGCCAGG ATCACGCCAT TGCACTCCAG CTGGGGCCAA 780
CAACAGCAAG ACTCCATCTC AAAAAAAAAA AAAAAAAAAA AGAAAAAGGA ATCTGAGCAT 840
GGAGGCACCC TCCACCTTCG GATTGCTAGG AGATCAATGT CTGGCCCCGA GTGGGTGAGG 900
CCAGCCGAGG TCACTTGAAG GGTATCAGCC CTGAGGAGGA GTTCACGGGG CCTCTTCCTC 960
TCGGCCAACC CCAGCAGAGC TTGGAAACTG AGGCCCAGAG CAGGAGTCCA GGCTCATAGA 1020
GCCGGCCTGG CAGAGGAGGG GTGGGGGAGT TGCGTCCCCA CCATTCCCAC TGGGGCATAC 1080
AGCGCCTTTC TGAGCGTCAC AGGCCTGTCT GTGTCCTTCT TTTGCGGAAG AACTAACCAC 1140
ACCTCAGGTT CCCCTTATGA AAGACAGAGG CTGAGGAGAG TGAGTCAGTT TTATTATATG 1200
AGATAAGGCG GCTGGACAAA GCAGCGACAC AGGGACTGGC ACACAGACAG TGCTCAGCGA 1260
AGCAGTCGCC TTCCTTCAGG TCTGAAATCC TCACTCAGCT CCCCAGCTTC TCTGGGGGAT 1320
CTCCCTTCCC CTCTCTGGAC CCCTGGGCCT GACTTCCCCC ACTACTCCCA GCCTTTGTCC 1380
CACTCCTGCC CCAGGCACCC CTCCCTCCTT CATGGGAAAT GGAGCTTCCT CCTCTGGTCC 1440
TGCCACCACC TTCCTGGTGA GGGTCGGGCT CTGCTGGGAG TGCCAGAGCT GCCCAGCCTG 1500
CTGACTCAGC GCCTGGGGAT AGGGCTTGCT TTAGGAACAG CCCAGGCCTC GGGCAAACAG 1560
AGCCACGGCA ACCACACCCC TGCCACAGGA ATGCAGCAAC ATTCCTGGGG GGTGCCGTGG 1620
CACCGTGCCT GTGACTGGGG GGCAGGTGGG GGGCAGGTAG ACACCTGCCT CTGTTACCTT 1680
GCCACAGGTA GAAGGGAGCC AGGAGTCAGG GCCCAGTGTC CTGGGGCAGG GGGATGGAGT 1740
GAGGTCATGA GGCTTTGAAA TCTGTACCAG CCATGTGACT TGAACAAGGC CTCTCTGAGC 1800
CTCAGTTTCC TCACCTGTAA GGTGAAGGGA GAATAGCGGT AGCCTTCTGG TGGGCTTATG 1860
GGGAGGACTG AACGAGAGTG CGCCCGTCTG GGGCTCAGCA TCAGCCTGCC TCACCGTGAG 1920
GATTCCGTGA AGCAGACCCT CACCCCTGTA ATAGAATCAG GGGGTCTTCT GGCTCTGGGC 1980
CCTAGAATGG GGCTGAAGCC CAGAGAGGCA GTTGCACCTC CCCTAGGCCA CACAGCAGGT 2040
ATAGGCCCCA GGGGCTGAGT GCCCATCATG CCTGCCCTCC TCTCCATCCA CCCAGAGCCT 2100
CACTAGCCAG ACCCGCACTC TCCCATCCCC TGGGCAAGTC TGCACCCCAG GTCGGTGAGG 2160
ACTCCCAGAT TCTACTCCCA CCAGCCAGGG CCAGACCTGG TGCAGGAGGC TCCACAGTTC 2220
TCCTGCTCGG GGCTCCGTCT CCCCACTTCC TGGAGCTCCA TCCAAGTGGG GAACCCTGCC 2280
CGTCCTCTGC CCCTCAAGCC AACCAGGCAT TTACGGGGGA 2320