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

TagContent
EnhancerAtlas ID
HS032-00259 
Organism
Homo sapiens 
Tissue/cell
DLD1 
Coordinate
chr12:6290770-6293190 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7342306chr126291093hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SP1MA0079.4chr12:6291837-6291852AGAGGGCGTGGCCTG-6.15
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_00985chr12:6290507-6292062Adrenal_Gland
SE_00985chr12:6292206-6292982Adrenal_Gland
SE_01613chr12:6290594-6292119Aorta
SE_01613chr12:6292178-6293897Aorta
SE_03988chr12:6290792-6291792Brain_Anterior_Caudate
SE_04905chr12:6289324-6293306Brain_Cingulate_Gyrus
SE_05857chr12:6287388-6293430Brain_Hippocampus_Middle
SE_07876chr12:6289745-6293464Brain_Inferior_Temporal_Lobe
SE_23086chr12:6290753-6292057Colon_Crypt_1
SE_23086chr12:6292201-6293938Colon_Crypt_1
SE_23760chr12:6290811-6292000Colon_Crypt_2
SE_23760chr12:6292242-6293084Colon_Crypt_2
SE_24754chr12:6291005-6292084Colon_Crypt_3
SE_24754chr12:6292220-6293863Colon_Crypt_3
SE_25881chr12:6290586-6291938Duodenum_Smooth_Muscle
SE_25881chr12:6292265-6293935Duodenum_Smooth_Muscle
SE_26531chr12:6290619-6292172Esophagus
SE_26531chr12:6292175-6293815Esophagus
SE_27879chr12:6290695-6293924Fetal_Intestine
SE_28805chr12:6290511-6293953Fetal_Intestine_Large
SE_30052chr12:6290681-6292144Fetal_Muscle
SE_31631chr12:6290651-6293026Gastric
SE_34881chr12:6288010-6291925HeLa
SE_37709chr12:6286475-6292578HSMMtube
SE_37940chr12:6286549-6293824HUVEC
SE_41013chr12:6288021-6292951Left_Ventricle
SE_42122chr12:6287877-6292200Lung
SE_42122chr12:6292204-6293894Lung
SE_48662chr12:6287969-6292096Right_Atrium
SE_50072chr12:6290476-6292094Sigmoid_Colon
SE_50072chr12:6292172-6294061Sigmoid_Colon
SE_52457chr12:6287948-6292107Small_Intestine
SE_52457chr12:6292166-6294018Small_Intestine
SE_53862chr12:6287321-6293849Spleen
SE_54512chr12:6288437-6293993Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1262922476292800
chr1262913586291755
Number: 1             
IDChromosomeStartEnd
GH12I006177chr1262869856293820
Enhancer Sequence
TAATGAGTTT GGGTTTTACC CCCAAGAAAC TGGGGGTAAA AGAGGGAATA AAAGCAAAAC 60
ATCCCATGCC CTCAAGGAAC GTCTAGTCCA GGATTAGAAG TGGGGCAGTC CCAGGAAGGA 120
GCCATCTTGA CAGTGAATTC ACGCGGAAGA CGCGTGAACC CAGCTGGCCT GGAGAGACAG 180
AGGTGCTTTG CAGGGCATGG GGAAGCCAGC AGGTCCCAGT CGAGAAACCT GGTTTTCTGT 240
CTGGGTTGGT TGAAGACTCT TTGTCCCAGA AGGAGTCGCT TGTTTGCTTG TTCATCTTAA 300
GTTTAAATTG AGAGAGGTTA ACGGCTTTTG CCTCAGAAGG CAGGCTGGCC TGGCAGGGTG 360
TGTGTTGTGA GGTGCAGAAA CACATCTTCC CCAGCTGGCC TCACAGGCCA AGAAGCAGAT 420
AATGTCTTCC TTCTGCCAGC TTCCCCGCAG CTTGGTTTTC CTGGGACAGT TCCTCCGCTG 480
GAGGAAGGGA CAGGGGATGG GGACAGGGGA TGGAGGAGGA GTTGGGGAGA CCCTTCAGAG 540
AGTGTGGCAG AAACACGTGT GTACAGGCTG GCACACGAGT CACAGAGGCA ACAGGGTGGC 600
TGCGGGGAGA AATGTGAGCA GAGCTCATGC AATTGTCGTG AGTGAGTGCG CTCTCGCGGC 660
TCTAAGGATT TGGGAAAACA ACTTGCAGAT CCAGGCATGT TTACGTAGGG AGGGGTGCCG 720
TGTGCTGGAC CAGGTCCAGA ACTAAAAATA ACACAGTATT TCTGTGCCCA GCAAGAGCGC 780
TAGCATCTGT GGGGTTTGCG TGGTGGGAAG AGTGTGGTTT CAGCTGAACC AGGCGCAGTG 840
TGACCAGAAC AGTAGGAGGG AAGGCCAGGC CTGGGTGGGA GGCCCCAGGA TGGGCGGGGG 900
AAGGACTGAG GGCGAAGGCC ATCCCAACTC GCAGCAGAAA AAGCCTCCAG GCGGTCACGG 960
GCTGCCCATC TCGTGAGGCC AGATGTGGGT CCTCCTGCAT ATCTGAAACA GCACAGAGCA 1020
TTGGGGCAGC CTCCAAACCT CCCCTATAAG GAGCAGTTAA GGGATCCAGA GGGCGTGGCC 1080
TGGAGCAGAG AGAAGGGAAG CAACATGTGT GGGGCATTCA CAAGTGCAGG ATGCCTTCTC 1140
CGGGCTCCCA TGATGATCCA GACAGGTAGG CGTTTTCCTT CCCTTTTTGC AGATTGTGAA 1200
AACAGCGTTC AAAAAAGACT CATGGGCCGG GCGCGGTGGA TCACGCCTGT AATCCCAGCA 1260
CTTTGGGAGG CCAAGGCAGG CAGATCACAA GGCCAGGAGT TGAAGACCAA CCTGGCCAAC 1320
ATGATGAAAC CCTGTCTCTA CTAAAAATAC AAAAATTAGC CGGACGTGAT GGTGGGCACC 1380
TGTAATCCCA GCTACTCAGG AGGCTGAGGC AGGAGAATCG CTTGAAACCG GAAGGCAGAG 1440
GTTGCAGTGA GCCGAGATTG CGCCACTGCA CTCCAGCCTG GTCAATAAGA GTGAAACTCT 1500
GTCTCAAAAA CAAACCAACC AACAAACCAA AAACTCTTGT AACCCTGGGG CCACCCAGCC 1560
ACAAAGAGGC AGGGCTGGGA CAGGCCCCTG CAAGTCTCCT CTGGAAGGCC AAAGGGCTGC 1620
TACTAGGAAG GGGTGGCAGA CTCATCCCAT GTGGCTTCAG AGGGCAGGAC ATGGACAAAG 1680
GTTATGGGAA GGGAGGGAAA CTTTCCAATA ACCAGACTGC ACAAGAGTGG AGTGGCCTGC 1740
CTCAGGAGGG GTAAGCTCAT GCAAAAGCTG GCTGTTGGGG ACATTGGGAG GGACTCTGAA 1800
GGTCACCACC ACTCTGAATC AATGCTGTGT GGGAGGATGC CAGGGTCCAC TGGACCCATG 1860
ACGTGCCTTT AGCGTGGGAA GCAGGGAACC TCAACTTTGG AAAGAGTGAG GGCACAGTGA 1920
TGTCCAGCCA CTCCCAGAAG CCGTCTGTTA ATAGAGCAAC CCCTCGGGCG GTGTGCAATC 1980
CTAATGACCA GCCCCAGGAC ATTGGAAACA GGGTCCTGCT GACCACAGTC TAGGAGACAG 2040
GGCTGCACAC AGACGGAACC AAGCACACAA GACGAGAGAG GGTGTGTACC GCAGAAACCA 2100
AGGGCTCATT TATGTGCTGC GTTCTCAGTC TGCAAGGAGT CAGAAGAGAG GACAGTGAGG 2160
CCAGGAGAAC TCAGGGAACA CTCCTTGTTG TAATCATCAC AGTTATGTAA CTCATATTAC 2220
CAGCTGTTCT TTCGTGAGCA TTCTCTATGT GCCAGGCTAA GTGTTTTGTA TGCACTGTAT 2280
GATTTAATCC TAGAACAACA CTATGAAGCA GGAGCTCTTA GTATTCCCCT TTTACAGATG 2340
AGGAGGCAGG CTCAGAGAGG TGATGTAACT TGCCCAGAAT TATATAACTA GTGTGTGGCA 2400
GAGCCTGGAC TCAAGCCCAG 2420