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

TagContent
EnhancerAtlas ID
HS101-47443 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chrX:106971990-106973600 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxa2MA0047.2chrX:106973041-106973053CCTGTGTAAACA-6.14
NFAT5MA0606.1chrX:106971993-106972003AATGGAAAAT-6.02
NFATC1MA0624.1chrX:106971993-106972003AATGGAAAAT-6.02
NFATC3MA0625.1chrX:106971993-106972003AATGGAAAAT-6.02
SOX10MA0442.2chrX:106973532-106973543TGCTTTGTTTT-6.02
SP2MA0516.2chrX:106972075-106972092TAGTGGGAGGGGCTTCT-6.07
ZNF263MA0528.1chrX:106972887-106972908GAGGGAGGCAGGGGAGTGGGG+6.01
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_01071chrX:106971618-106973280Adrenal_Gland
SE_01966chrX:106971864-106974686Aorta
SE_03516chrX:106971928-106973355Brain_Angular_Gyrus
SE_04216chrX:106971962-106973919Brain_Anterior_Caudate
SE_05145chrX:106970990-106976266Brain_Cingulate_Gyrus
SE_06059chrX:106971025-106978046Brain_Hippocampus_Middle
SE_07082chrX:106970975-106974311Brain_Hippocampus_Middle_150
SE_08011chrX:106970753-106974165Brain_Inferior_Temporal_Lobe
SE_26851chrX:106971490-106973171Esophagus
SE_26851chrX:106973240-106976214Esophagus
SE_31551chrX:106971546-106976348Gastric
SE_37687chrX:106971467-106974436HSMMtube
SE_40984chrX:106971295-106976264Left_Ventricle
SE_42016chrX:106972041-106973265LNCaP
SE_42016chrX:106973387-106974623LNCaP
SE_42321chrX:106971517-106976299Lung
SE_46769chrX:106972014-106974259Ovary
SE_48198chrX:106968365-106976212Psoas_Muscle
SE_48777chrX:106971518-106973164Right_Atrium
SE_48777chrX:106973323-106976136Right_Atrium
SE_50259chrX:106971450-106973176Sigmoid_Colon
SE_50259chrX:106973383-106976185Sigmoid_Colon
SE_51615chrX:106969635-106976277Skeletal_Muscle
SE_52487chrX:106972184-106972832Small_Intestine
SE_54817chrX:106970985-106975637Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chrX106973000106973062
Number: 1             
IDChromosomeStartEnd
GH0XI107727chrX106971071106976328
Enhancer Sequence
TAAAATGGAA AATCTTTCTC AGAAGGGGAA TTGTTTAGTT TTTCTCAGGG AAGGGATGTG 60
ATGACCTGCC TCAGCTTGGT CAGAATAGTG GGAGGGGCTT CTGGGAGAAG CAACCCAGGC 120
TGGCTAAGTA TAGACTGGTG GGGTGCTGCC TAGGGTGGGG CCTCACAATG GGTCCTGGTT 180
ATCTGGTGGC CTTGGGATTT CAGGGGACAG GCAAATGTGG CCAAATATTG AAGACTCGCT 240
GGCAAGAAAC CAAACTGCCT CTGAGTGGGC AGCTTTAAGA GGAGTAGAGT TTAGGGCAAA 300
GGAGATTGTT TTCTCCTTCT GTTCTTGGTA AATGAAAGCA AGCTGTTATG AAGATGTCGT 360
GAGGAGCAGC AAGGCTGCCT TGGGCATATT GGGGATGTTA ATCTTCAGTG CTCCCTGCCT 420
GGGAGACCCC GTTTGCTTGC TCATCAAAAC ATCCTCCCTG GGTGCATCCT CCCCCAGCTC 480
TACTGCCTCA TTTATACGGT GGCATAGCTG AGAAATTAAC CCCCAGAAGA GTCTGTGGCT 540
GCTGGGGTTG ATGGATTCTC CTTCCCTGGG GTAATTTCTT TTTACCAAGA GCCTGCTGCG 600
AACCCAAAGG AATGAGTCTA GTGGGAGAAA TTCCAGGCAG AAGGGCAGGA CGCTGGAGGA 660
GCTTTCTTTG ACCATTTTCT GCTACTTTCT GCTGGCAGTG GCCTTCTCTG CCTGTGAACT 720
AGGCAGCCCT GGCAGCAGAA ACAATACTGA CACTAGAGCT GGCGAGGGAA GCCCTTGCCC 780
CTCATCACCA CTCCTTTTTG CCCTTGTAAA ATTCTGGAAA AACCTCAGCC CTGGAGCTCC 840
CTCTAGTTTG ACCAGGTGAT AGCCAACTCC CTGACACCAG GCAGAGCTGG GCCGACAGAG 900
GGAGGCAGGG GAGTGGGGCT GGGCATCCCC CTCTCCACCC CCGGGGCCCT GTTGTGAGGT 960
GTTGACAGCT GGGAGAGGAC CTGAAACCAG TTAGCCTGGG GCTCCCAGCC AGCAGTGTAT 1020
TTTCATCTTG TTTTGACTGG GACCGTCCTC CCCTGTGTAA ACACATCCAT GTCAGGGGGA 1080
AGAAAATGTA GAACAGCTTA AAATAAGTGG GCGGAATGCC TCCCACTCAT GAATCACCAG 1140
TGCAGGGAAT GCCCCGCAGG TGGGCCTTGC TTTAAGCAAA CCTGACATTA TGAAAATTTT 1200
AACTTAACAA GAGGGCAGGG ATGGACAGCT GTTAGGACTT GACCTACCTC TGGGAGATCT 1260
CAAAGCCTCA TTGGGTCCAA ATAATATCAG CAGCTCCCAT GTACTGATTG CTTAGTGGGC 1320
ACTGCGCTAA AGACATTAGA TAACGTTAAT TTTTTGAATC TTGTCAACGC TGTTAGGAGT 1380
TGGGTATTAC CTTATCATTA GACCCATTTT GTGGATGAGG AAACTGAGGC TCAGAGAGGT 1440
TAAATAACTT GCCTGGGATT ACACAGCAAG CAAATGGCAG AGATCAGATG AAACTCCCTG 1500
GTGTGTGATT TTAAAGCACT GGGCTGCCTC TAGCTGGAGT TGTGCTTTGT TTTGAGGAGG 1560
GCTCCAGGCC CAGCTGCACT CCAGGCAGCA ACTGGAACCT GCACTAGTGT 1610