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

TagContent
EnhancerAtlas ID
HS039-01667 
Organism
Homo sapiens 
Tissue/cell
ESC_NPC 
Coordinate
chr12:6331010-6332430 
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
ATTAGCCAGG ATTAGCGGCA TGCACCTGTA ATCCCAGCTA CTCAGGAGGC TGAGGTGGAA 60
GAATGGCTTG AGCCCAGGAG TCCAAGGCTA CAGTGAGCTA TGATTGCACC ACTGCACTCC 120
AGCCTGGGTG ACGAGAGCAA GACCCTGTCT CAAAAAATAA AGCAGCTGGG GTGAAAGCCG 180
GATGGGGACA GGGGAGCCCC TCTATGCCAC ACCAGAAAGT GAGTTCTCCT AGAAAATACT 240
TCAGAGCGCC TTAGATAGCG CTGCCTGACA ACCATGAAAG GCATTATTGG GTGGCACTGG 300
TTATACAAGT TTTGTGACCC TGTGACCCCA AGCCATTGTG ACTCAGCCAA CTGGAGCAAT 360
GTCTCCAACA GCGTTACAGA AAATGGGGCA GCTGATGGTT CACATAGCAT CCCCCCCGGC 420
CGGTGAACTC AGTCATTCTG TCAGAAAAGG CAGCAGGGTT CACTCCTGAT TTTTGTCCAA 480
GTGTTCCCAG TCATGCCCCT GGCCCTCCCT TTTCTCTGGG TTACTTGAAC CTTTCTCCTC 540
TCTTATTGTG AGTTGTTAAG CCTGTGAGAC CGAGACCTAT GGCAGCTTTT CCCATTTCTC 600
CAGAGCCAGC TGCTTTTCCT TCCTGGTTGT AGTGAAATGT TGTAGCTTTG ACAACCAAGC 660
CGCATGATGT AAGGTTTAAG GTGGGGTCCG AATGCGGGGG ACTCCCGACT CCGGGCTTGG 720
CCTGGCCCTT GGCCAAGATA AGAGACCTGA GATGCTTCCT TTTCCCTCGT GGTTCCAGTT 780
CTCCAGCCCA GCATCCTTCT TACCACCTGT GCACAGAGAC CGGATCAATG ACTGGACTTA 840
ACATATTGGC TCAGGGTCCT CGACATTGGG GCTCTCTATA AGATGGAAGG GGCCTTACCC 900
CTGGAGGTTC CACTGGGGTA CCCTGTCATT ATCTGAGCGT GGAACATTCC CAGAGAGACG 960
CAGCTCCTGC TCGTGAGAGG CTGCTGTGCA GAGCGTAGCT TTACCTCATC TTACAGCTTA 1020
GTTCCTTGGC AGACCTGGGA TTGTTTTCGT TCTTTTCTGC GACTCAGTTT TCCCAGCAGA 1080
TAAGGGGTGG GGTCATAACT TCACTCATCA GGGGAAGTAA GATGACTTGG GAGATAATTG 1140
CTTGATAAGC ACAAGCCTAG AGCAAAAAGG ACAGTAATGA GCACTGTCTC GCTATCTCCC 1200
TATGCGCGCA AGAGCATCAC AAGACCAGGG CGAGAGGGAG GACCAGGGTG AGAAACAGGT 1260
TGTGGCTAAA CGTGGACCAA AATTGAGCAC CGGCCTACAG TTTTCAGGTT AACGCTTTTA 1320
TGTCCAGGAG GCCAGCAGCT TCAGTCTTCC ATTCCCAGGG GACTGACTGG GCCTCCCTGG 1380
GGTTGGGGTG GAAGGAGGGA AGGTATCACC TTTGTACTTT 1420