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

TagContent
EnhancerAtlas ID
HS060-07343 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr12:6291660-6293010 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SP1MA0079.4chr12:6291837-6291852AGAGGGCGTGGCCTG-6.15
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_00985chr12:6290507-6292062Adrenal_Gland
SE_00985chr12:6292206-6292982Adrenal_Gland
SE_01613chr12:6290594-6292119Aorta
SE_01613chr12:6292178-6293897Aorta
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: 1             
ChromosomeStartEnd
chr1262922476292800
Number: 1             
IDChromosomeStartEnd
GH12I006177chr1262869856293820
Enhancer Sequence
TGGGCGGGGG AAGGACTGAG GGCGAAGGCC ATCCCAACTC GCAGCAGAAA AAGCCTCCAG 60
GCGGTCACGG GCTGCCCATC TCGTGAGGCC AGATGTGGGT CCTCCTGCAT ATCTGAAACA 120
GCACAGAGCA TTGGGGCAGC CTCCAAACCT CCCCTATAAG GAGCAGTTAA GGGATCCAGA 180
GGGCGTGGCC TGGAGCAGAG AGAAGGGAAG CAACATGTGT GGGGCATTCA CAAGTGCAGG 240
ATGCCTTCTC CGGGCTCCCA TGATGATCCA GACAGGTAGG CGTTTTCCTT CCCTTTTTGC 300
AGATTGTGAA AACAGCGTTC AAAAAAGACT CATGGGCCGG GCGCGGTGGA TCACGCCTGT 360
AATCCCAGCA CTTTGGGAGG CCAAGGCAGG CAGATCACAA GGCCAGGAGT TGAAGACCAA 420
CCTGGCCAAC ATGATGAAAC CCTGTCTCTA CTAAAAATAC AAAAATTAGC CGGACGTGAT 480
GGTGGGCACC TGTAATCCCA GCTACTCAGG AGGCTGAGGC AGGAGAATCG CTTGAAACCG 540
GAAGGCAGAG GTTGCAGTGA GCCGAGATTG CGCCACTGCA CTCCAGCCTG GTCAATAAGA 600
GTGAAACTCT GTCTCAAAAA CAAACCAACC AACAAACCAA AAACTCTTGT AACCCTGGGG 660
CCACCCAGCC ACAAAGAGGC AGGGCTGGGA CAGGCCCCTG CAAGTCTCCT CTGGAAGGCC 720
AAAGGGCTGC TACTAGGAAG GGGTGGCAGA CTCATCCCAT GTGGCTTCAG AGGGCAGGAC 780
ATGGACAAAG GTTATGGGAA GGGAGGGAAA CTTTCCAATA ACCAGACTGC ACAAGAGTGG 840
AGTGGCCTGC CTCAGGAGGG GTAAGCTCAT GCAAAAGCTG GCTGTTGGGG ACATTGGGAG 900
GGACTCTGAA GGTCACCACC ACTCTGAATC AATGCTGTGT GGGAGGATGC CAGGGTCCAC 960
TGGACCCATG ACGTGCCTTT AGCGTGGGAA GCAGGGAACC TCAACTTTGG AAAGAGTGAG 1020
GGCACAGTGA TGTCCAGCCA CTCCCAGAAG CCGTCTGTTA ATAGAGCAAC CCCTCGGGCG 1080
GTGTGCAATC CTAATGACCA GCCCCAGGAC ATTGGAAACA GGGTCCTGCT GACCACAGTC 1140
TAGGAGACAG GGCTGCACAC AGACGGAACC AAGCACACAA GACGAGAGAG GGTGTGTACC 1200
GCAGAAACCA AGGGCTCATT TATGTGCTGC GTTCTCAGTC TGCAAGGAGT CAGAAGAGAG 1260
GACAGTGAGG CCAGGAGAAC TCAGGGAACA CTCCTTGTTG TAATCATCAC AGTTATGTAA 1320
CTCATATTAC CAGCTGTTCT TTCGTGAGCA 1350