EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS193-00312 
Organism
Homo sapiens 
Tissue/cell
U87 
Coordinate
chr1:16507530-16510190 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7538216chr116509671hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ArntlMA0603.1chr1:16510043-16510053GGTCACGTGC+6.02
ELF3MA0640.1chr1:16508229-16508242CTACTTCCGGCTA-6.25
EWSR1-FLI1MA0149.1chr1:16508479-16508497GGGAGGAAGGAAGCAGAG+6.42
Nr2f6(var.2)MA0728.1chr1:16509417-16509432GAGGTCAGGAGTTCA+6.22
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_23091chr1:16507977-16509332Colon_Crypt_1
SE_24743chr1:16508183-16508861Colon_Crypt_3
SE_26540chr1:16504790-16512175Esophagus
SE_28102chr1:16507825-16509373Fetal_Intestine
SE_29455chr1:16507734-16509371Fetal_Intestine_Large
SE_31527chr1:16507486-16509710Gastric
SE_31527chr1:16509851-16511737Gastric
SE_34268chr1:16506936-16512113HCT-116
SE_34628chr1:16506549-16512234HeLa
SE_36144chr1:16507720-16509431HMEC
SE_38062chr1:16507125-16509874HUVEC
SE_40833chr1:16507342-16509479Left_Ventricle
SE_44998chr1:16507356-16509449NHLF
SE_46140chr1:16507347-16510631Osteoblasts
SE_47009chr1:16507488-16507895Ovary
SE_47009chr1:16508039-16509386Ovary
SE_47150chr1:16499250-16512083Panc1
SE_47539chr1:16507579-16507933Pancreas
SE_47539chr1:16507961-16508560Pancreas
SE_47539chr1:16508587-16509159Pancreas
SE_48744chr1:16507441-16509527Right_Atrium
SE_50427chr1:16507395-16509522Sigmoid_Colon
SE_52536chr1:16507445-16509419Small_Intestine
SE_56795chr1:16507333-16512008VACO_400
SE_57357chr1:16508000-16508578VACO_503
SE_57357chr1:16508592-16509318VACO_503
SE_57939chr1:16507977-16509011VACO_9m
SE_64726chr1:16507942-16511421NHEK
SE_65472chr1:16507356-16509554Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr11650808616509162
chr11650995016510149
chr11650840216508642
Number: 1             
IDChromosomeStartEnd
GH01I016171chr11649794116511884
Enhancer Sequence
TACCGAACTG GCCAGTGCAG CTCTAAAAGG TCAGCAGCAT GTGAGTGGGA GAGCTGGGCC 60
TGGCTGTGTG TTATTCACGT TCTTGAGTGT TGGCTTTCCA CAGTTTGGGC CTCTGGCAGC 120
AGAATCACCT GGGAAGCCAA AACTTCAGAT CCCTGGGATC CCAGACCCAC TGAATCAGAA 180
TCTCCGAGGC CAGGGCTTGG GCGTCTGCCC GTTCACCACA CACCCCAGCT GATTCTGATG 240
CACATGAGGT CAAGTTTGAA ACCCACCCCA CTGCCCTAGT TGTTCAAGAC TCCCAGCGCT 300
GGCTGGATGC AAAGTCTTAT GCCTGTAATC CCAGCTCTTT TGGGAGGCCA AGGCGGGCAG 360
ATCACTTGAG GTCAGGAGTT CGAGACCAGC CGGGCCTACA GAGTGAAACC CCGTCTCTAC 420
TAAAAATACA AAAATTAGCT AGGTGTGGTG GTGGGCGCCT GTAATCCCAG GAGGTGGAGG 480
TTGCAGTGAG CCGAGATCGC GCCGCTGCAC TGCATCCTGG GCAACAGAGC GGGACTCCGT 540
CTCAAAAAAA AAAAAAGACT CCCGGCCAGG AAGAGAGCTT GAATGAAGTC TGACCTGCAC 600
CAGGCCTTCT GGGCCCAGAC CAGGCCTGCT TAGGGGCATG TGCCCTGCTC AGAACTTCCC 660
CATCCCAGCT AACCCAGAAG ATAGCTGGGA TGAAGATAGC TACTTCCGGC TACCAGCCCA 720
TGATTCTTTG CCAGCCTGCA CTGTTCCCTG AAGAGCAAAA AGACTTGGAA TTTCCCTGCT 780
CTATCCAGAG GGGCTGGGAT GAGGGGTCCT GAGTTCCCTT ATCCCATGTC CTACCAACCT 840
CTGGAGCTCT CCAGTCAGCC AGCTCGAGGC TCTGGCCCTA GCTGGTGGGC AATGGGAGGG 900
AGAGGCTTGG CCCAGCACCC CACCCCACAG ATCAGCCTGG TCCGGCAAGG GGAGGAAGGA 960
AGCAGAGGCA GCCTGGGCCA GCGGACACAG GGTTGGGGGT GACACAGGCC TCAGGAATTT 1020
GAAAACAAAC ACTTCGCCAG GGAAGGAAGA GGCTGCTGTT GGCTGCTGAG CCCGGGCGGG 1080
CCCAGGTCCC TCCCTTTCAG GGCAGGGGTG AATCCCAGTG CTGCTGACCA TGGCCCCCGG 1140
CTGGACCCAG TGCTCGGGGA GTTTCCACTC CGCTGGTGGG ATGGGAAGGT CATGGGAGGT 1200
GTGGGGGGAT CCAGGCTCTG TCCAGATACG GGAGCATCCT GGCTGGGGTG AGGACAGGAA 1260
GGGACAAAGA GCTGGGAAAG CCACGAGACC CCAGGAGAAG GCTCAGCAGC AACAGGATGC 1320
CGCCTCAAGC ATTTATTGAG CACCCATGGT ATTCCAAAAA CTGAGAATAT AAGCACTGCC 1380
TAGCTGGGGA GATCAGGGGA AGCCTAGAGC CCTGTGGCCT TCCTGGAGGA GGTGGCATTG 1440
AACTGAGCCC TGAAAGGTAA ACTAGGACCG GGGAGGACAG AATCTTACAA GTCTCCCCCC 1500
TTCACACTCC CAGAGCCGGC GCTCAGTGAG TGCATGAGTG AGTAAGCGGC TGACCAGCGA 1560
CTATGCAGCA TGAATGAATG ACAGACTGAA TGACATGAAG CCTGGAGTCT CAAGGCCGAG 1620
ACTGCAAAAG AAGAGTCCAT CCTCCTATCC CCTCTGCTCT GAACTCTCTT CATGATCCTG 1680
AAGGTGCTTG GTACCTGGAG ACTACGGAGC CAGCCTGCCG GGGTTCTAGT CTGAACTCAG 1740
TCACTTCCCA GCTGTGTAAC TTTGGACAAG TTACTTAACC TCTCTGTGCC TCTGGTCCCT 1800
TCTCTGTAAA GTGTAGTCAT CGGCCGGGCG TGGTGGCTCA CGCCTGTAAT CCCAGCACTT 1860
TGGGAGGCCA AGGCAGACGA ATCACTTGAG GTCAGGAGTT CAAGACCAGC CTGCCCAACA 1920
TGGTGAAACC CTGTCTCTAC TAAAAACACA AAAATCAGCC GGGTGTCGGG GGCAGGCACC 1980
TGTAATCCCA GCTACTCGGG AGGCTAAGGC ACGAGAATTG CTTGAACCCG GGAGGCGGAG 2040
GTTGCAGTGA GCTGACATCT CGCCACTGCA CTCCAGCCTG GGCAACAGAG TGAGACTCAA 2100
AAAAAAAAAA AAAAAATACA GAGGTAATCA TAGTGCCTCC TTCACAGGGT TTTTGAGAGG 2160
ACTGAATGAG TTTTACAAGT GAAGTGCTTA GAACGACGTT GCACATGTAG TGAGAACTAC 2220
ATGAGTGTTG GCCAATGCTA TTACTGAGGT TCCAGCTTAC GCGTTCATTG AGTCACTCAC 2280
TCACTCACTG TTCATTCACT GATTCGCTCC TACATGCCAT CCGCCACTTA CACACCCCTC 2340
CCTCTTCACC GTCATCTGTT AAGCAATCCC CGTGTGCCCG GCTCTCTCCT CTCGGTCCTC 2400
CCAGCCCCCC TTTGCCAGTC TTGGATGGTG CCCGCCGTGC TGCCAATTAC CCTAACAATT 2460
TCATTAATTC CTCTCAAGCC CAAAACAAAC AAGAAGGACC TATCTGGAGC AGGGGTCACG 2520
TGCTAAGACC AGAAGCAGGT GTGGGACAAA CCCTCTAGGA CGAGTTCTTT GACCAGAGTT 2580
CATCACCGGA GCTGCTCCAG AGATGGCCAG GCCTCCCCAC CTGCAGGTGC CCGGCCAGTG 2640
CCCCCCACCC CGGGCAGCCT 2660