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

TagContent
EnhancerAtlas ID
HS180-10568 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr12:6330920-6332610 
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: 2             
ChromosomeStartEnd
chr1263309766331800
chr1263320556332244
Number: 1             
IDChromosomeStartEnd
GH12I006213chr1263222806345639
Enhancer Sequence
TGCTTGAGGC CAGGAATTTA AGACCAGCCT GAGCAACATA GCGAGACCCC TGGCTCTACA 60
AAAAAAAAAA AAAAAAAAAG GGTTTAAAAT ATTAGCCAGG ATTAGCGGCA TGCACCTGTA 120
ATCCCAGCTA CTCAGGAGGC TGAGGTGGAA GAATGGCTTG AGCCCAGGAG TCCAAGGCTA 180
CAGTGAGCTA TGATTGCACC ACTGCACTCC AGCCTGGGTG ACGAGAGCAA GACCCTGTCT 240
CAAAAAATAA AGCAGCTGGG GTGAAAGCCG GATGGGGACA GGGGAGCCCC TCTATGCCAC 300
ACCAGAAAGT GAGTTCTCCT AGAAAATACT TCAGAGCGCC TTAGATAGCG CTGCCTGACA 360
ACCATGAAAG GCATTATTGG GTGGCACTGG TTATACAAGT TTTGTGACCC TGTGACCCCA 420
AGCCATTGTG ACTCAGCCAA CTGGAGCAAT GTCTCCAACA GCGTTACAGA AAATGGGGCA 480
GCTGATGGTT CACATAGCAT CCCCCCCGGC CGGTGAACTC AGTCATTCTG TCAGAAAAGG 540
CAGCAGGGTT CACTCCTGAT TTTTGTCCAA GTGTTCCCAG TCATGCCCCT GGCCCTCCCT 600
TTTCTCTGGG TTACTTGAAC CTTTCTCCTC TCTTATTGTG AGTTGTTAAG CCTGTGAGAC 660
CGAGACCTAT GGCAGCTTTT CCCATTTCTC CAGAGCCAGC TGCTTTTCCT TCCTGGTTGT 720
AGTGAAATGT TGTAGCTTTG ACAACCAAGC CGCATGATGT AAGGTTTAAG GTGGGGTCCG 780
AATGCGGGGG ACTCCCGACT CCGGGCTTGG CCTGGCCCTT GGCCAAGATA AGAGACCTGA 840
GATGCTTCCT TTTCCCTCGT GGTTCCAGTT CTCCAGCCCA GCATCCTTCT TACCACCTGT 900
GCACAGAGAC CGGATCAATG ACTGGACTTA ACATATTGGC TCAGGGTCCT CGACATTGGG 960
GCTCTCTATA AGATGGAAGG GGCCTTACCC CTGGAGGTTC CACTGGGGTA CCCTGTCATT 1020
ATCTGAGCGT GGAACATTCC CAGAGAGACG CAGCTCCTGC TCGTGAGAGG CTGCTGTGCA 1080
GAGCGTAGCT TTACCTCATC TTACAGCTTA GTTCCTTGGC AGACCTGGGA TTGTTTTCGT 1140
TCTTTTCTGC GACTCAGTTT TCCCAGCAGA TAAGGGGTGG GGTCATAACT TCACTCATCA 1200
GGGGAAGTAA GATGACTTGG GAGATAATTG CTTGATAAGC ACAAGCCTAG AGCAAAAAGG 1260
ACAGTAATGA GCACTGTCTC GCTATCTCCC TATGCGCGCA AGAGCATCAC AAGACCAGGG 1320
CGAGAGGGAG GACCAGGGTG AGAAACAGGT TGTGGCTAAA CGTGGACCAA AATTGAGCAC 1380
CGGCCTACAG TTTTCAGGTT AACGCTTTTA TGTCCAGGAG GCCAGCAGCT TCAGTCTTCC 1440
ATTCCCAGGG GACTGACTGG GCCTCCCTGG GGTTGGGGTG GAAGGAGGGA AGGTATCACC 1500
TTTGTACTTT TTTTTTTTTT TTTTTGAGAG GGAGTCTCGC TCTGTCGCCC AGGCTGGAGT 1560
GCAGTGGCGC AATCTCCGCT CACTGCAAGC TCCGCCTCCC GGGCTCACGC CATTCTCCTG 1620
CCTCAGCCTC TGGAGTAGCT GGGACTACAG GCGCCCGCCA CCACGCCTGG AGAATTTTTT 1680
GTATTTTTAG 1690