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

TagContent
EnhancerAtlas ID
HS095-06583 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr12:6290900-6292900 
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
CAGTGAATTC ACGCGGAAGA CGCGTGAACC CAGCTGGCCT GGAGAGACAG AGGTGCTTTG 60
CAGGGCATGG GGAAGCCAGC AGGTCCCAGT CGAGAAACCT GGTTTTCTGT CTGGGTTGGT 120
TGAAGACTCT TTGTCCCAGA AGGAGTCGCT TGTTTGCTTG TTCATCTTAA GTTTAAATTG 180
AGAGAGGTTA ACGGCTTTTG CCTCAGAAGG CAGGCTGGCC TGGCAGGGTG TGTGTTGTGA 240
GGTGCAGAAA CACATCTTCC CCAGCTGGCC TCACAGGCCA AGAAGCAGAT AATGTCTTCC 300
TTCTGCCAGC TTCCCCGCAG CTTGGTTTTC CTGGGACAGT TCCTCCGCTG GAGGAAGGGA 360
CAGGGGATGG GGACAGGGGA TGGAGGAGGA GTTGGGGAGA CCCTTCAGAG AGTGTGGCAG 420
AAACACGTGT GTACAGGCTG GCACACGAGT CACAGAGGCA ACAGGGTGGC TGCGGGGAGA 480
AATGTGAGCA GAGCTCATGC AATTGTCGTG AGTGAGTGCG CTCTCGCGGC TCTAAGGATT 540
TGGGAAAACA ACTTGCAGAT CCAGGCATGT TTACGTAGGG AGGGGTGCCG TGTGCTGGAC 600
CAGGTCCAGA ACTAAAAATA ACACAGTATT TCTGTGCCCA GCAAGAGCGC TAGCATCTGT 660
GGGGTTTGCG TGGTGGGAAG AGTGTGGTTT CAGCTGAACC AGGCGCAGTG TGACCAGAAC 720
AGTAGGAGGG AAGGCCAGGC CTGGGTGGGA GGCCCCAGGA TGGGCGGGGG AAGGACTGAG 780
GGCGAAGGCC ATCCCAACTC GCAGCAGAAA AAGCCTCCAG GCGGTCACGG GCTGCCCATC 840
TCGTGAGGCC AGATGTGGGT CCTCCTGCAT ATCTGAAACA GCACAGAGCA TTGGGGCAGC 900
CTCCAAACCT CCCCTATAAG GAGCAGTTAA GGGATCCAGA GGGCGTGGCC TGGAGCAGAG 960
AGAAGGGAAG CAACATGTGT GGGGCATTCA CAAGTGCAGG ATGCCTTCTC CGGGCTCCCA 1020
TGATGATCCA GACAGGTAGG CGTTTTCCTT CCCTTTTTGC AGATTGTGAA AACAGCGTTC 1080
AAAAAAGACT CATGGGCCGG GCGCGGTGGA TCACGCCTGT AATCCCAGCA CTTTGGGAGG 1140
CCAAGGCAGG CAGATCACAA GGCCAGGAGT TGAAGACCAA CCTGGCCAAC ATGATGAAAC 1200
CCTGTCTCTA CTAAAAATAC AAAAATTAGC CGGACGTGAT GGTGGGCACC TGTAATCCCA 1260
GCTACTCAGG AGGCTGAGGC AGGAGAATCG CTTGAAACCG GAAGGCAGAG GTTGCAGTGA 1320
GCCGAGATTG CGCCACTGCA CTCCAGCCTG GTCAATAAGA GTGAAACTCT GTCTCAAAAA 1380
CAAACCAACC AACAAACCAA AAACTCTTGT AACCCTGGGG CCACCCAGCC ACAAAGAGGC 1440
AGGGCTGGGA CAGGCCCCTG CAAGTCTCCT CTGGAAGGCC AAAGGGCTGC TACTAGGAAG 1500
GGGTGGCAGA CTCATCCCAT GTGGCTTCAG AGGGCAGGAC ATGGACAAAG GTTATGGGAA 1560
GGGAGGGAAA CTTTCCAATA ACCAGACTGC ACAAGAGTGG AGTGGCCTGC CTCAGGAGGG 1620
GTAAGCTCAT GCAAAAGCTG GCTGTTGGGG ACATTGGGAG GGACTCTGAA GGTCACCACC 1680
ACTCTGAATC AATGCTGTGT GGGAGGATGC CAGGGTCCAC TGGACCCATG ACGTGCCTTT 1740
AGCGTGGGAA GCAGGGAACC TCAACTTTGG AAAGAGTGAG GGCACAGTGA TGTCCAGCCA 1800
CTCCCAGAAG CCGTCTGTTA ATAGAGCAAC CCCTCGGGCG GTGTGCAATC CTAATGACCA 1860
GCCCCAGGAC ATTGGAAACA GGGTCCTGCT GACCACAGTC TAGGAGACAG GGCTGCACAC 1920
AGACGGAACC AAGCACACAA GACGAGAGAG GGTGTGTACC GCAGAAACCA AGGGCTCATT 1980
TATGTGCTGC GTTCTCAGTC 2000