EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS180-00518 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:16497960-16501220 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:16498199-16498217CCTGCCTTCCTCACCTCC-6.24
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: 3             
ChromosomeStartEnd
chr11649960716500371
chr11649801416498132
chr11649976116499895
Number: 1             
IDChromosomeStartEnd
GH01I016171chr11649794116511884
Enhancer Sequence
TGAAGGGGGG GGGGCTGCCT GCAGCTCCAA CCCTGTAATA GACCCTCCCT GTCTCGCCAG 60
CGACGGGCGG TAATAACTGT TTTGCCCAGC AGAACTGCCT CATGCCATAG CTTGAGAATG 120
TGCCTCGGGG CCCGTCTGCA GAGACCACCC CCCAGTCAGG GCAGCCGGGC CAGACCTCGC 180
CCAAGCCTGA CCCTAGGCTG ATCCCTGGGA GGAGTAGGGA TCTCTGGGCC CTGCCCTGCC 240
CTGCCTTCCT CACCTCCAAG TTGGCCTCAG CAGGCCCAGC AGGTGAAGGG CCCAGGCCCT 300
GGGCAGCCCT GCGAGTCAGT GCTACGTCTG CCCGCCTCTG CCTTCAGATC ACAAACTTCC 360
CGAAGATAAG AGGTGGTGAC TCCTCTAGCA GACTGGAGGG CTCTTCCGGA AATGGAGTAT 420
ATGTCCCCTC CTCAGAGGGC AGAGGCTGTG GCTTCCCCAT GAGAGTGGAG GCTTCAGCAG 480
GACAGAGGCC AGGCCTCTGC TATCAGACTA GGAGCTCCCT GAGGGCAGAG GCTGTGGGAT 540
ATTCCCGGGG CAGAGGTGAC CTTCCCCCAT CAGACTGGGA CCTCAGCTCA GTCCAGCAGC 600
TCTACGGTGA ATGTCTCCGA GGGAGGGGCA TTAGCACAAC AGACACTGCC TCTCAGCCCC 660
GAGTCCCCAG ATCCATGTCA TCTATTGGAG TCTCCCCCAC TGTAAACCTG CAAGGGCAGC 720
CACGGCCGGG AGCAGCTGGT CCTGAGACTT GGGCAGAGGC CCTGGACAGT GGGGCAGAAG 780
CGCTTGGCTG GCCAGGAATT GGATCACTGC CCCCTCCCAC CCCACCCCAT TCAGCCCTGT 840
CTCCCACGGA CTCTGACCAC CCCTTGGTTC TCTTATCAAA AACCGCCAAA ACCCGCCATC 900
GAAACTCCCA GCCTCCTGAC CCCCATGCCC CACCCGGCTC CACCCGTCTT CCCAACCTGG 960
CATCCAGTGC CCCAAACCTG CCTATTCCGT TCCTGGGAAG ACCCAGAAGG GAGCAGAGCT 1020
GGCACCAGGA GGCCAACAAC CCAGGCCCCC TCCGTCCCTA GCCCCTCCTG GCCCTGGGCC 1080
CTCCACCCTA CTGTTTCTCC TGGGGTGTGC CTTTCTTTGC CTTATGCCTC GGCATCTCTA 1140
AGTGGCAGGG GATGGAGTGG AGTGAGGGCG GCAGGCCAAG GGCATGGCCC ATAATGAAAA 1200
AGGAATCTGG TTGGGCATGG TGGCTCACCC TTGTAATCTC AGCACTTTGG GAGGCCAAGG 1260
CAGGCAGATC ATGAGGTCAG GAGATCGAGA GCAGCCTAGC CAACATGGTG AAACCCCGTC 1320
TCTACTAAAA ACACAAAAAT TAGCTGGACG TGGTGGTGGG CGCCTGTAAT CCCAGCTACT 1380
CGGGAGGCTG AGGCAGGAGA ATTGCTGGAA CCCGGGAGGT GGAGGTTGCA GTGAGCCAGG 1440
ATCACGCCAT TGCACTCCAG CTGGGGCCAA CAACAGCAAG ACTCCATCTC AAAAAAAAAA 1500
AAAAAAAAAA AGAAAAAGGA ATCTGAGCAT GGAGGCACCC TCCACCTTCG GATTGCTAGG 1560
AGATCAATGT CTGGCCCCGA GTGGGTGAGG CCAGCCGAGG TCACTTGAAG GGTATCAGCC 1620
CTGAGGAGGA GTTCACGGGG CCTCTTCCTC TCGGCCAACC CCAGCAGAGC TTGGAAACTG 1680
AGGCCCAGAG CAGGAGTCCA GGCTCATAGA GCCGGCCTGG CAGAGGAGGG GTGGGGGAGT 1740
TGCGTCCCCA CCATTCCCAC TGGGGCATAC AGCGCCTTTC TGAGCGTCAC AGGCCTGTCT 1800
GTGTCCTTCT TTTGCGGAAG AACTAACCAC ACCTCAGGTT CCCCTTATGA AAGACAGAGG 1860
CTGAGGAGAG TGAGTCAGTT TTATTATATG AGATAAGGCG GCTGGACAAA GCAGCGACAC 1920
AGGGACTGGC ACACAGACAG TGCTCAGCGA AGCAGTCGCC TTCCTTCAGG TCTGAAATCC 1980
TCACTCAGCT CCCCAGCTTC TCTGGGGGAT CTCCCTTCCC CTCTCTGGAC CCCTGGGCCT 2040
GACTTCCCCC ACTACTCCCA GCCTTTGTCC CACTCCTGCC CCAGGCACCC CTCCCTCCTT 2100
CATGGGAAAT GGAGCTTCCT CCTCTGGTCC TGCCACCACC TTCCTGGTGA GGGTCGGGCT 2160
CTGCTGGGAG TGCCAGAGCT GCCCAGCCTG CTGACTCAGC GCCTGGGGAT AGGGCTTGCT 2220
TTAGGAACAG CCCAGGCCTC GGGCAAACAG AGCCACGGCA ACCACACCCC TGCCACAGGA 2280
ATGCAGCAAC ATTCCTGGGG GGTGCCGTGG CACCGTGCCT GTGACTGGGG GGCAGGTGGG 2340
GGGCAGGTAG ACACCTGCCT CTGTTACCTT GCCACAGGTA GAAGGGAGCC AGGAGTCAGG 2400
GCCCAGTGTC CTGGGGCAGG GGGATGGAGT GAGGTCATGA GGCTTTGAAA TCTGTACCAG 2460
CCATGTGACT TGAACAAGGC CTCTCTGAGC CTCAGTTTCC TCACCTGTAA GGTGAAGGGA 2520
GAATAGCGGT AGCCTTCTGG TGGGCTTATG GGGAGGACTG AACGAGAGTG CGCCCGTCTG 2580
GGGCTCAGCA TCAGCCTGCC TCACCGTGAG GATTCCGTGA AGCAGACCCT CACCCCTGTA 2640
ATAGAATCAG GGGGTCTTCT GGCTCTGGGC CCTAGAATGG GGCTGAAGCC CAGAGAGGCA 2700
GTTGCACCTC CCCTAGGCCA CACAGCAGGT ATAGGCCCCA GGGGCTGAGT GCCCATCATG 2760
CCTGCCCTCC TCTCCATCCA CCCAGAGCCT CACTAGCCAG ACCCGCACTC TCCCATCCCC 2820
TGGGCAAGTC TGCACCCCAG GTCGGTGAGG ACTCCCAGAT TCTACTCCCA CCAGCCAGGG 2880
CCAGACCTGG TGCAGGAGGC TCCACAGTTC TCCTGCTCGG GGCTCCGTCT CCCCACTTCC 2940
TGGAGCTCCA TCCAAGTGGG GAACCCTGCC CGTCCTCTGC CCCTCAAGCC AACCAGGCAT 3000
TTACGGGGGA TGGGGCAGGG AGGGAGGCCA GGACCTGCAT CCTTCCAGCC CTGGCCCTCA 3060
GCAACCCCAT CAGGCAGTCA GGGGAGGAGC CTCCCCCAGG GAATCCTCCC TCCCTCTGTG 3120
TTGGCCTGGC CAGGTTCTCC TCTCTCTGTC TGCCTTTGTC TTTTTCTCTC TGTCTCTTCA 3180
TCCCAGGAAG AGGCCACAGG ACAGGGGTGT CCCAAGCACA GAAGAAACTT GTCTGATGAA 3240
AACAGGCCTT GGCTGGGAGC 3260