EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS076-00717 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr1:16498080-16500540 
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: 28             
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_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
TGCCTCGGGG CCCGTCTGCA GAGACCACCC CCCAGTCAGG GCAGCCGGGC CAGACCTCGC 60
CCAAGCCTGA CCCTAGGCTG ATCCCTGGGA GGAGTAGGGA TCTCTGGGCC CTGCCCTGCC 120
CTGCCTTCCT CACCTCCAAG TTGGCCTCAG CAGGCCCAGC AGGTGAAGGG CCCAGGCCCT 180
GGGCAGCCCT GCGAGTCAGT GCTACGTCTG CCCGCCTCTG CCTTCAGATC ACAAACTTCC 240
CGAAGATAAG AGGTGGTGAC TCCTCTAGCA GACTGGAGGG CTCTTCCGGA AATGGAGTAT 300
ATGTCCCCTC CTCAGAGGGC AGAGGCTGTG GCTTCCCCAT GAGAGTGGAG GCTTCAGCAG 360
GACAGAGGCC AGGCCTCTGC TATCAGACTA GGAGCTCCCT GAGGGCAGAG GCTGTGGGAT 420
ATTCCCGGGG CAGAGGTGAC CTTCCCCCAT CAGACTGGGA CCTCAGCTCA GTCCAGCAGC 480
TCTACGGTGA ATGTCTCCGA GGGAGGGGCA TTAGCACAAC AGACACTGCC TCTCAGCCCC 540
GAGTCCCCAG ATCCATGTCA TCTATTGGAG TCTCCCCCAC TGTAAACCTG CAAGGGCAGC 600
CACGGCCGGG AGCAGCTGGT CCTGAGACTT GGGCAGAGGC CCTGGACAGT GGGGCAGAAG 660
CGCTTGGCTG GCCAGGAATT GGATCACTGC CCCCTCCCAC CCCACCCCAT TCAGCCCTGT 720
CTCCCACGGA CTCTGACCAC CCCTTGGTTC TCTTATCAAA AACCGCCAAA ACCCGCCATC 780
GAAACTCCCA GCCTCCTGAC CCCCATGCCC CACCCGGCTC CACCCGTCTT CCCAACCTGG 840
CATCCAGTGC CCCAAACCTG CCTATTCCGT TCCTGGGAAG ACCCAGAAGG GAGCAGAGCT 900
GGCACCAGGA GGCCAACAAC CCAGGCCCCC TCCGTCCCTA GCCCCTCCTG GCCCTGGGCC 960
CTCCACCCTA CTGTTTCTCC TGGGGTGTGC CTTTCTTTGC CTTATGCCTC GGCATCTCTA 1020
AGTGGCAGGG GATGGAGTGG AGTGAGGGCG GCAGGCCAAG GGCATGGCCC ATAATGAAAA 1080
AGGAATCTGG TTGGGCATGG TGGCTCACCC TTGTAATCTC AGCACTTTGG GAGGCCAAGG 1140
CAGGCAGATC ATGAGGTCAG GAGATCGAGA GCAGCCTAGC CAACATGGTG AAACCCCGTC 1200
TCTACTAAAA ACACAAAAAT TAGCTGGACG TGGTGGTGGG CGCCTGTAAT CCCAGCTACT 1260
CGGGAGGCTG AGGCAGGAGA ATTGCTGGAA CCCGGGAGGT GGAGGTTGCA GTGAGCCAGG 1320
ATCACGCCAT TGCACTCCAG CTGGGGCCAA CAACAGCAAG ACTCCATCTC AAAAAAAAAA 1380
AAAAAAAAAA AGAAAAAGGA ATCTGAGCAT GGAGGCACCC TCCACCTTCG GATTGCTAGG 1440
AGATCAATGT CTGGCCCCGA GTGGGTGAGG CCAGCCGAGG TCACTTGAAG GGTATCAGCC 1500
CTGAGGAGGA GTTCACGGGG CCTCTTCCTC TCGGCCAACC CCAGCAGAGC TTGGAAACTG 1560
AGGCCCAGAG CAGGAGTCCA GGCTCATAGA GCCGGCCTGG CAGAGGAGGG GTGGGGGAGT 1620
TGCGTCCCCA CCATTCCCAC TGGGGCATAC AGCGCCTTTC TGAGCGTCAC AGGCCTGTCT 1680
GTGTCCTTCT TTTGCGGAAG AACTAACCAC ACCTCAGGTT CCCCTTATGA AAGACAGAGG 1740
CTGAGGAGAG TGAGTCAGTT TTATTATATG AGATAAGGCG GCTGGACAAA GCAGCGACAC 1800
AGGGACTGGC ACACAGACAG TGCTCAGCGA AGCAGTCGCC TTCCTTCAGG TCTGAAATCC 1860
TCACTCAGCT CCCCAGCTTC TCTGGGGGAT CTCCCTTCCC CTCTCTGGAC CCCTGGGCCT 1920
GACTTCCCCC ACTACTCCCA GCCTTTGTCC CACTCCTGCC CCAGGCACCC CTCCCTCCTT 1980
CATGGGAAAT GGAGCTTCCT CCTCTGGTCC TGCCACCACC TTCCTGGTGA GGGTCGGGCT 2040
CTGCTGGGAG TGCCAGAGCT GCCCAGCCTG CTGACTCAGC GCCTGGGGAT AGGGCTTGCT 2100
TTAGGAACAG CCCAGGCCTC GGGCAAACAG AGCCACGGCA ACCACACCCC TGCCACAGGA 2160
ATGCAGCAAC ATTCCTGGGG GGTGCCGTGG CACCGTGCCT GTGACTGGGG GGCAGGTGGG 2220
GGGCAGGTAG ACACCTGCCT CTGTTACCTT GCCACAGGTA GAAGGGAGCC AGGAGTCAGG 2280
GCCCAGTGTC CTGGGGCAGG GGGATGGAGT GAGGTCATGA GGCTTTGAAA TCTGTACCAG 2340
CCATGTGACT TGAACAAGGC CTCTCTGAGC CTCAGTTTCC TCACCTGTAA GGTGAAGGGA 2400
GAATAGCGGT AGCCTTCTGG TGGGCTTATG GGGAGGACTG AACGAGAGTG CGCCCGTCTG 2460