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

TagContent
EnhancerAtlas ID
HS177-03131 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH_RA 
Coordinate
chr10:81001940-81002870 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr10:81002036-81002046GGGGCGGGGC-6.02
ZNF263MA0528.1chr10:81002845-81002866TTCCTCCCGCGCTCCTCCTCC-6.09
ZNF263MA0528.1chr10:81002351-81002372CCCTCCTCCACCCCCTCCCCG-6.43
ZNF263MA0528.1chr10:81002299-81002320TCCCCTCCCCTCCCCTCCCCT-6.91
ZNF263MA0528.1chr10:81002304-81002325TCCCCTCCCCTCCCCTCCCCC-7.81
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00967chr10:81001368-81009228Adrenal_Gland
SE_04037chr10:81000769-81002965Brain_Anterior_Caudate
SE_04933chr10:81000917-81002337Brain_Cingulate_Gyrus
SE_05772chr10:81000410-81002759Brain_Hippocampus_Middle
SE_06946chr10:81000453-81011029Brain_Hippocampus_Middle_150
SE_07838chr10:81000430-81002366Brain_Inferior_Temporal_Lobe
SE_09148chr10:81000344-81011517CD14
SE_11725chr10:81000940-81015628CD20
SE_24559chr10:81001777-81002742Colon_Crypt_2
SE_26499chr10:81000484-81002330Duodenum_Smooth_Muscle
SE_26661chr10:81000438-81010326Esophagus
SE_31588chr10:81000983-81010356Gastric
SE_40721chr10:81000448-81010508Left_Ventricle
SE_42200chr10:80994761-81011639Lung
SE_43896chr10:81001261-81011164MM1S
SE_45787chr10:81000400-81002733Osteoblasts
SE_47703chr10:81002333-81002951Pancreas
SE_48707chr10:80996610-81002855Right_Atrium
SE_50353chr10:81000694-81011674Sigmoid_Colon
SE_52824chr10:81000865-81002288Small_Intestine
SE_52824chr10:81002323-81010454Small_Intestine
SE_53282chr10:80994962-81011321Spleen
SE_54575chr10:81000811-81010193Stomach_Smooth_Muscle
SE_59543chr10:81001388-81026785Ly3
SE_61092chr10:80988661-81027750HBL1
SE_62376chr10:81000995-81055642Tonsil
SE_66905chr10:81000728-81010383H2171
SE_67368chr10:81001261-81011164MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr108100217581002268
Enhancer Sequence
GCAAGCGCTG AAAGCCCGGA GCCCTTGCGA CAGACTGGCT GGAAGGAAGA GGCCTCGGCC 60
ACCACAGGAT GCAATGTCAG GAAGGCAGCA GCTCCCGGGG CGGGGCAGGG CCGCGCGCAG 120
CCGCCCCCGG CTTCCCTCCT GCCGCCAGCT CCTGGTCACA GGAACTCCCC GAAGTCGGGG 180
AGCGGGAGCG TACGTGCGCG TGTTCACCCT GTCCTGGGCC CCTCGCTCGG GGAATCCCGG 240
GGGTGCCAGG GCACCCAGGG TCAGGGAAGT AAGATGCCGG GCCGCCTACC TTCTCCACCC 300
CGTAGCCCGT TCCGAAAATC CTTTAAACCG AGATTTAATC TGGATGCCTA GCCCCGCCCT 360
CCCCTCCCCT CCCCTCCCCT CCCCCCGGCC GAGGCCCCCT CCAGTTCAGC TCCCTCCTCC 420
ACCCCCTCCC CGCCGTGGAC CCTCATTAGC ATGCCCACTT GGGAGGATTC GCTGGGGGGC 480
GGGAGACACC CGAAGTCATC CACCGCCAGC GCCTTCCCGG CGGCCTCCTC GGGCGACAGC 540
GCTCCGGGAG CCCCACTCGC ACAAGTGTTG CTTCCAATTA ATTGCCTGGG CGGGGGAAGG 600
AAAGGGGCCT CGTCGCCGCC CCCGCCCGGA GGCTGGAGTG CTGCTCGTCG GGTCGTGCGT 660
TCGCTCGGCA GCGGCGTGCA CCAGCACCAC CCCTGCGTGC AAGTTTGAAA TGTGAGCTGC 720
CTCCGATTCA TACTCGCTCG CGCTCCCTCG CAGCGAAGTG GCTGGGCTGA CGGTCTGCGC 780
GCGCGAGTGA GTGCGGGCGG CGGGCTGGGG GGCGGGGTGC GGACGGCGAG GCTCGCGGGG 840
CGGGGAGGGC GCGCGCGAGC CGGGGCTCCC TGGAGACGCC AAGGCAGGTC TGCTCGCCTT 900
TCATCTTCCT CCCGCGCTCC TCCTCCTCCT 930