EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS094-00264 
Organism
Homo sapiens 
Tissue/cell
hMADS-3 
Coordinate
chr1:16507250-16510190 
Target genes
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
TCAGGCTGGA GTACGGTGGC GCAATCACAG CTCACTGCAA CCTCTGCCTT CTGGGCTCAA 60
GCCAGCCTCC TACCTCAGCC TCCTGAGTAG CCAGGACTAC AGGTGTACAC CACCACACCC 120
AGCTAATTTT TTGCGTGCTT TTTGTAGAGA TGGGGTTTCA CCATGTTGCC TAGTCTGGTC 180
TCGAACTCCT GACCTCAAGA GATCCACCCA CCTTGGATCC CAAAATGCTG GGATTACAGG 240
CATGAGCTAC TGCGCCCGGC CTCTAGATTT AAATAGTACC TACCGAACTG GCCAGTGCAG 300
CTCTAAAAGG TCAGCAGCAT GTGAGTGGGA GAGCTGGGCC TGGCTGTGTG TTATTCACGT 360
TCTTGAGTGT TGGCTTTCCA CAGTTTGGGC CTCTGGCAGC AGAATCACCT GGGAAGCCAA 420
AACTTCAGAT CCCTGGGATC CCAGACCCAC TGAATCAGAA TCTCCGAGGC CAGGGCTTGG 480
GCGTCTGCCC GTTCACCACA CACCCCAGCT GATTCTGATG CACATGAGGT CAAGTTTGAA 540
ACCCACCCCA CTGCCCTAGT TGTTCAAGAC TCCCAGCGCT GGCTGGATGC AAAGTCTTAT 600
GCCTGTAATC CCAGCTCTTT TGGGAGGCCA AGGCGGGCAG ATCACTTGAG GTCAGGAGTT 660
CGAGACCAGC CGGGCCTACA GAGTGAAACC CCGTCTCTAC TAAAAATACA AAAATTAGCT 720
AGGTGTGGTG GTGGGCGCCT GTAATCCCAG GAGGTGGAGG TTGCAGTGAG CCGAGATCGC 780
GCCGCTGCAC TGCATCCTGG GCAACAGAGC GGGACTCCGT CTCAAAAAAA AAAAAAGACT 840
CCCGGCCAGG AAGAGAGCTT GAATGAAGTC TGACCTGCAC CAGGCCTTCT GGGCCCAGAC 900
CAGGCCTGCT TAGGGGCATG TGCCCTGCTC AGAACTTCCC CATCCCAGCT AACCCAGAAG 960
ATAGCTGGGA TGAAGATAGC TACTTCCGGC TACCAGCCCA TGATTCTTTG CCAGCCTGCA 1020
CTGTTCCCTG AAGAGCAAAA AGACTTGGAA TTTCCCTGCT CTATCCAGAG GGGCTGGGAT 1080
GAGGGGTCCT GAGTTCCCTT ATCCCATGTC CTACCAACCT CTGGAGCTCT CCAGTCAGCC 1140
AGCTCGAGGC TCTGGCCCTA GCTGGTGGGC AATGGGAGGG AGAGGCTTGG CCCAGCACCC 1200
CACCCCACAG ATCAGCCTGG TCCGGCAAGG GGAGGAAGGA AGCAGAGGCA GCCTGGGCCA 1260
GCGGACACAG GGTTGGGGGT GACACAGGCC TCAGGAATTT GAAAACAAAC ACTTCGCCAG 1320
GGAAGGAAGA GGCTGCTGTT GGCTGCTGAG CCCGGGCGGG CCCAGGTCCC TCCCTTTCAG 1380
GGCAGGGGTG AATCCCAGTG CTGCTGACCA TGGCCCCCGG CTGGACCCAG TGCTCGGGGA 1440
GTTTCCACTC CGCTGGTGGG ATGGGAAGGT CATGGGAGGT GTGGGGGGAT CCAGGCTCTG 1500
TCCAGATACG GGAGCATCCT GGCTGGGGTG AGGACAGGAA GGGACAAAGA GCTGGGAAAG 1560
CCACGAGACC CCAGGAGAAG GCTCAGCAGC AACAGGATGC CGCCTCAAGC ATTTATTGAG 1620
CACCCATGGT ATTCCAAAAA CTGAGAATAT AAGCACTGCC TAGCTGGGGA GATCAGGGGA 1680
AGCCTAGAGC CCTGTGGCCT TCCTGGAGGA GGTGGCATTG AACTGAGCCC TGAAAGGTAA 1740
ACTAGGACCG GGGAGGACAG AATCTTACAA GTCTCCCCCC TTCACACTCC CAGAGCCGGC 1800
GCTCAGTGAG TGCATGAGTG AGTAAGCGGC TGACCAGCGA CTATGCAGCA TGAATGAATG 1860
ACAGACTGAA TGACATGAAG CCTGGAGTCT CAAGGCCGAG ACTGCAAAAG AAGAGTCCAT 1920
CCTCCTATCC CCTCTGCTCT GAACTCTCTT CATGATCCTG AAGGTGCTTG GTACCTGGAG 1980
ACTACGGAGC CAGCCTGCCG GGGTTCTAGT CTGAACTCAG TCACTTCCCA GCTGTGTAAC 2040
TTTGGACAAG TTACTTAACC TCTCTGTGCC TCTGGTCCCT TCTCTGTAAA GTGTAGTCAT 2100
CGGCCGGGCG TGGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCCA AGGCAGACGA 2160
ATCACTTGAG GTCAGGAGTT CAAGACCAGC CTGCCCAACA TGGTGAAACC CTGTCTCTAC 2220
TAAAAACACA AAAATCAGCC GGGTGTCGGG GGCAGGCACC TGTAATCCCA GCTACTCGGG 2280
AGGCTAAGGC ACGAGAATTG CTTGAACCCG GGAGGCGGAG GTTGCAGTGA GCTGACATCT 2340
CGCCACTGCA CTCCAGCCTG GGCAACAGAG TGAGACTCAA AAAAAAAAAA AAAAAATACA 2400
GAGGTAATCA TAGTGCCTCC TTCACAGGGT TTTTGAGAGG ACTGAATGAG TTTTACAAGT 2460
GAAGTGCTTA GAACGACGTT GCACATGTAG TGAGAACTAC ATGAGTGTTG GCCAATGCTA 2520
TTACTGAGGT TCCAGCTTAC GCGTTCATTG AGTCACTCAC TCACTCACTG TTCATTCACT 2580
GATTCGCTCC TACATGCCAT CCGCCACTTA CACACCCCTC CCTCTTCACC GTCATCTGTT 2640
AAGCAATCCC CGTGTGCCCG GCTCTCTCCT CTCGGTCCTC CCAGCCCCCC TTTGCCAGTC 2700
TTGGATGGTG CCCGCCGTGC TGCCAATTAC CCTAACAATT TCATTAATTC CTCTCAAGCC 2760
CAAAACAAAC AAGAAGGACC TATCTGGAGC AGGGGTCACG TGCTAAGACC AGAAGCAGGT 2820
GTGGGACAAA CCCTCTAGGA CGAGTTCTTT GACCAGAGTT CATCACCGGA GCTGCTCCAG 2880
AGATGGCCAG GCCTCCCCAC CTGCAGGTGC CCGGCCAGTG CCCCCCACCC CGGGCAGCCT 2940