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

TagContent
EnhancerAtlas ID
HS111-03722 
Organism
Homo sapiens 
Tissue/cell
KB 
Coordinate
chr3:193858140-193860830 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MAXMA0058.3chr3:193860247-193860257AGCACGTGGT-6.02
ZfxMA0146.2chr3:193859479-193859493CAGGCCTAGGCCGC-7.38
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_01349chr3:193858420-193860752Adrenal_Gland
SE_02677chr3:193858037-193859322Astrocytes
SE_02677chr3:193859408-193860621Astrocytes
SE_23549chr3:193858230-193860171Colon_Crypt_1
SE_24246chr3:193858298-193860039Colon_Crypt_2
SE_25250chr3:193858327-193860171Colon_Crypt_3
SE_26775chr3:193858136-193860952Esophagus
SE_27968chr3:193847154-193860776Fetal_Intestine
SE_28994chr3:193847120-193860668Fetal_Intestine_Large
SE_31540chr3:193858222-193860889Gastric
SE_33897chr3:193853845-193859368HCC1954
SE_33897chr3:193859457-193861692HCC1954
SE_35209chr3:193857560-193861167HeLa
SE_36526chr3:193852114-193859361HMEC
SE_36526chr3:193859372-193860857HMEC
SE_38168chr3:193850622-193861237HUVEC
SE_41422chr3:193858180-193860841Left_Ventricle
SE_42942chr3:193858151-193860890Lung
SE_47560chr3:193858231-193859387Pancreas
SE_47560chr3:193859392-193860761Pancreas
SE_48520chr3:193858213-193860813Psoas_Muscle
SE_49415chr3:193858215-193860789Right_Atrium
SE_50956chr3:193858142-193860794Sigmoid_Colon
SE_53101chr3:193858128-193860741Small_Intestine
SE_54294chr3:193856634-193860592Spleen
SE_56835chr3:193856473-193860716VACO_400
SE_57499chr3:193858308-193860686VACO_503
SE_58014chr3:193858255-193860603VACO_9m
SE_60119chr3:193805468-193860641Ly4
SE_63450chr3:193848453-193860739NCI-H69
SE_64646chr3:193852085-193860721NHEK
SE_65385chr3:193856882-193859389Pancreatic_islets
SE_65385chr3:193859421-193860922Pancreatic_islets
SE_67229chr3:193858490-193860707MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr3193859199193859624
Enhancer Sequence
AATATCACCG AAAGTACATA GATATCTTCC TAGGGAGGGG ACTAAATCAA AGGAAAAACA 60
CAAATACGTT TTTTTCTTTT TTTTAATTGG TGATTTGAAA AGAGCACTTT TTTTCCCCCT 120
GAAAGCTAGG TTTAGACTAT TCCACGAGGA TTTTTTCTTT GTTACAGTAA GGGGAGAAGG 180
TGGAGACCCC ACTAGGCTCC AAACCGGAAA GGGCACTTTC CAGTTCCTGC CCAGCTATGC 240
CACCAAATTC ACTGTGTCAC CTTGGATAAG TCATTTCCCT TCTCTGGGTC ATTTCCAAGT 300
CTGGAAAATG AATGGACTTA TTTCTAAGAC GCTGTACCCT CCTGCACTTT GGCTGTTTCT 360
GGAGTAAGTA GCTGAGGGAG AGGCGAAACT TCAAAAACGA CTTCAATGAT GTTGCCTCCC 420
TGGGGGTCCC TCAGGCCTGG CCTAATTATA CGGCCTCGGG CACACCAGCA GCCCCTCTCG 480
CCGGCCCCCA GCAGTGCTGA TCGCTCGGGG AGATAAGGCA CGACTCCAAA CTGCGTCCGG 540
ATGCGGGCCG CGGGCCCCGG CTGCCGCGCG CATTAGCCTC TCAATGGAGC CCTTCCGGGG 600
CCCCGGCCCC CCGCCGTCTC CAGCAGCATC CGGAGCGGGA AAGGCGCCGA ACTGGAAGGG 660
GGTGGGGGTG CTCTTCGGTC AACACGAGAG CCCTCTCCAA GCGCAGAAGC GCGACTCCGG 720
AGGCTCGCCC CTCCTCGCGC CCCGTCCCAC CCCACGCGTT TCTGGAATGG GGACCCTGGG 780
GTTTCGTTGG ACCCCCTCGT CGTCACCACC GTCCCGGGAA ACCTGTCATT AAAGTCAATT 840
AACTTTTCCC ACACCCGTTG GCCGGTAACA ACCCGCTCCT AGCTTCCTCC CCGGCTCCTA 900
AGTGCAACCA GATGGGCGGA CGGGCTGCCC CCGCCGCGCG CCCGCCGGGG CGGCCCGGGG 960
GTTCCAGGGA GGCCGCCCGG GGCCCTCCGC CCGGGCGGGA GCCGGCCAGG GCGGCCACGC 1020
CGGGCCAGCC CTGGCGGCCC TGCGGCCAAG GTGGTTCGCT TAGCAGGCCC GGCTGCTTTC 1080
TGGCAGGAAA TGAATAGCTC CCAGATGAGC TCAGGCAACC TGAGAGGTCG TGAGAACGGC 1140
GCGAACCCCC GCCTGTGCAG CCGGCAGCCT GCCAGGCCGC GGGGGGAGCG GGCGGCGGCG 1200
GCGGCGGCGG CGGGAGGCCG GGAGGCCCGG CGGGCGGGCG GGCGGGCGGC GCTGACACAC 1260
GAGCCCGCGC CCGCTCCCGC TGACAGGCAG GCCGCCGCCC CCGCTTCCCC CGCCCCGGGC 1320
CCCAGCGCCT CCCAAGCAGC AGGCCTAGGC CGCAGGAAGG CGGCCGCGCG GCCCCGCCGG 1380
GCCTGGGGGT GGGGCCGCCT GCCAGTGTTT TTCCAGTTCC CCCGGTAGCT CCGGGCCGCA 1440
TTTAGTAGCT GGGGAAACTG GGCCGAGGCC AGGGCCGGGG CACTAGAGGC CCTCGCGGCC 1500
CGCAGAGCCC TGCCAGGCGG CAGGCCACGC CGGGGCAGGA GTGGGCAGAG CGGCGGGGTG 1560
AGGCCATCCC AGCCCACAGA GCCGTCCCAA AAAAGACCTT GCCACCAGAC AGCAACCCTG 1620
GACGCCTAAA AAAAAAATCC TCATTTCTGA AAACCCTGAG CGCCTACTGA GTGCTCAGCA 1680
GGCCCAATTC CCACCAGCCT CCGCCGCACC GAGCTCCCTG TGTAGCCGGG GAGATCCACA 1740
AACACCCTCG TGACTCATCC CAGGTTTGAT GTGCTAAGTG CCAAAACTGA AGTTTAAACA 1800
AAGGGCACCT AGAACAGAGA GATTAATTCT GATGAGAGGA AACCAGGCCG GGGAGGTTTT 1860
TCAGAGTTGG CACTTGAAGC CGAGAGGTGA AAGATGAGTT CAACAGGAAG GGTTAGAAGC 1920
AGAAGGGTGA GGGAAAACGC GGAGATGAAC ATATATACGT CCAGTCTGGG GAGATGTCAG 1980
TATGTTTACC ATGGTGTGGT ATCTAAGTTT TCAAATATAC AAATTGGCTT AGAGGTCAAA 2040
AAAAGAAAAA GAGGGATAAG CCCTGCCGCA GTGGTTGGCT TAAATGCAAT ACAGCCCAGG 2100
GGTTAGAAGC ACGTGGTCTG GCTCCTGGCG GCTTGGCTTA GGTTTTGAGC CCGAGGGAAA 2160
TTACTGAACT CCCTGCCTCA ATTTTGTAAC TCTGTATCTC ATTTGTAACT TAGGGCTCGT 2220
CAGGGTAGTG CTTCACAGGG TTGAGAAGAT GAAATGAGTA CATGCACTTA AAGCATTTAG 2280
AATAGTGCTG TCAGCTCTTC GGATTCTTAA CCACAGTGAG GGACGTTCAC CAGACAAGAA 2340
AGCCAGTCCC GGCCTTTGCC CAGCGATGGC AGGATCTGCT TGTAATTGCA CCAGGCCCTA 2400
GGTGAAAGGA CCACTGCTTC TTCCTTAGTT TCTGAATTTC ATGCATTCAT TTGATAATTA 2460
TTGAACCAGG CACTATGGGA ATAAAGGGAG AAGAAAGGCA TGGTCTCTGT AACTATAAAG 2520
CTATCTGGTA GACAAGACAG CTTCCACACA AGAACAGCAC TGCTGGGCGC GGTGGCTCAC 2580
GCCTGTAATC CCAGCACTTT GGGAGGCCAA GGCGGGTGGA TCACAAGGTC AGGAGATCGA 2640
GACCATCTTG GCTAACATGG TGAAACCCCG TTTCTACTAA AAATACAAAA 2690