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

TagContent
EnhancerAtlas ID
HS116-07789 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr12:6331080-6332430 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EBF1MA0154.3chr12:6332360-6332374ATTCCCAGGGGACT-6.59
EBF1MA0154.3chr12:6332360-6332374ATTCCCAGGGGACT+6.74
EWSR1-FLI1MA0149.1chr12:6332399-6332417GGAAGGAGGGAAGGTATC+6.45
EWSR1-FLI1MA0149.1chr12:6332395-6332413GGGTGGAAGGAGGGAAGG+6.56
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_01613chr12:6331068-6332334Aorta
SE_03308chr12:6331173-6332411Brain_Angular_Gyrus
SE_03988chr12:6328807-6336415Brain_Anterior_Caudate
SE_04905chr12:6328630-6346354Brain_Cingulate_Gyrus
SE_05857chr12:6328573-6346408Brain_Hippocampus_Middle
SE_06790chr12:6328750-6346091Brain_Hippocampus_Middle_150
SE_07876chr12:6328735-6347463Brain_Inferior_Temporal_Lobe
SE_08879chr12:6331617-6331845Brain_Mid_Frontal_Lobe
SE_08879chr12:6331934-6332225Brain_Mid_Frontal_Lobe
SE_23086chr12:6330958-6332424Colon_Crypt_1
SE_23760chr12:6331109-6332358Colon_Crypt_2
SE_24754chr12:6331065-6332427Colon_Crypt_3
SE_25881chr12:6331138-6332492Duodenum_Smooth_Muscle
SE_26531chr12:6328841-6332525Esophagus
SE_27879chr12:6330794-6343416Fetal_Intestine
SE_28805chr12:6330455-6345849Fetal_Intestine_Large
SE_31631chr12:6330908-6332515Gastric
SE_33937chr12:6330804-6332438HCC1954
SE_35850chr12:6331075-6332437HMEC
SE_37940chr12:6328841-6332447HUVEC
SE_41591chr12:6331083-6332422LNCaP
SE_42122chr12:6328842-6332515Lung
SE_48662chr12:6331176-6332445Right_Atrium
SE_50072chr12:6330980-6332462Sigmoid_Colon
SE_52457chr12:6330890-6332501Small_Intestine
SE_54512chr12:6320070-6346293Stomach_Smooth_Muscle
SE_57134chr12:6331268-6332449VACO_400
SE_57526chr12:6331004-6332437VACO_503
SE_57940chr12:6331422-6332473VACO_9m
SE_64246chr12:6331037-6332392NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1263320556332244
Number: 1             
IDChromosomeStartEnd
GH12I006213chr1263222806345639
Enhancer Sequence
AGCCCAGGAG TCCAAGGCTA CAGTGAGCTA TGATTGCACC ACTGCACTCC AGCCTGGGTG 60
ACGAGAGCAA GACCCTGTCT CAAAAAATAA AGCAGCTGGG GTGAAAGCCG GATGGGGACA 120
GGGGAGCCCC TCTATGCCAC ACCAGAAAGT GAGTTCTCCT AGAAAATACT TCAGAGCGCC 180
TTAGATAGCG CTGCCTGACA ACCATGAAAG GCATTATTGG GTGGCACTGG TTATACAAGT 240
TTTGTGACCC TGTGACCCCA AGCCATTGTG ACTCAGCCAA CTGGAGCAAT GTCTCCAACA 300
GCGTTACAGA AAATGGGGCA GCTGATGGTT CACATAGCAT CCCCCCCGGC CGGTGAACTC 360
AGTCATTCTG TCAGAAAAGG CAGCAGGGTT CACTCCTGAT TTTTGTCCAA GTGTTCCCAG 420
TCATGCCCCT GGCCCTCCCT TTTCTCTGGG TTACTTGAAC CTTTCTCCTC TCTTATTGTG 480
AGTTGTTAAG CCTGTGAGAC CGAGACCTAT GGCAGCTTTT CCCATTTCTC CAGAGCCAGC 540
TGCTTTTCCT TCCTGGTTGT AGTGAAATGT TGTAGCTTTG ACAACCAAGC CGCATGATGT 600
AAGGTTTAAG GTGGGGTCCG AATGCGGGGG ACTCCCGACT CCGGGCTTGG CCTGGCCCTT 660
GGCCAAGATA AGAGACCTGA GATGCTTCCT TTTCCCTCGT GGTTCCAGTT CTCCAGCCCA 720
GCATCCTTCT TACCACCTGT GCACAGAGAC CGGATCAATG ACTGGACTTA ACATATTGGC 780
TCAGGGTCCT CGACATTGGG GCTCTCTATA AGATGGAAGG GGCCTTACCC CTGGAGGTTC 840
CACTGGGGTA CCCTGTCATT ATCTGAGCGT GGAACATTCC CAGAGAGACG CAGCTCCTGC 900
TCGTGAGAGG CTGCTGTGCA GAGCGTAGCT TTACCTCATC TTACAGCTTA GTTCCTTGGC 960
AGACCTGGGA TTGTTTTCGT TCTTTTCTGC GACTCAGTTT TCCCAGCAGA TAAGGGGTGG 1020
GGTCATAACT TCACTCATCA GGGGAAGTAA GATGACTTGG GAGATAATTG CTTGATAAGC 1080
ACAAGCCTAG AGCAAAAAGG ACAGTAATGA GCACTGTCTC GCTATCTCCC TATGCGCGCA 1140
AGAGCATCAC AAGACCAGGG CGAGAGGGAG GACCAGGGTG AGAAACAGGT TGTGGCTAAA 1200
CGTGGACCAA AATTGAGCAC CGGCCTACAG TTTTCAGGTT AACGCTTTTA TGTCCAGGAG 1260
GCCAGCAGCT TCAGTCTTCC ATTCCCAGGG GACTGACTGG GCCTCCCTGG GGTTGGGGTG 1320
GAAGGAGGGA AGGTATCACC TTTGTACTTT 1350