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

TagContent
EnhancerAtlas ID
HS182-05973 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr13:99129950-99131510 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs912330chr1399131294hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr13:99129967-99129988TCTCCCATCTCCTCCTTCACC-6.03
ZNF263MA0528.1chr13:99130247-99130268GGGGAACGAGGAGGAAGGGGA+6.13
ZNF263MA0528.1chr13:99129964-99129985CCATCTCCCATCTCCTCCTTC-6.24
ZNF263MA0528.1chr13:99130256-99130277GGAGGAAGGGGAGAAAAAGAG+6.78
ZNF263MA0528.1chr13:99130253-99130274CGAGGAGGAAGGGGAGAAAAA+6.7
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_11626chr13:99127788-99131320CD20
SE_27318chr13:99129890-99130939Esophagus
SE_32245chr13:99130242-99130932Gastric
SE_32245chr13:99131024-99131531Gastric
SE_37511chr13:99127619-99131417HSMMtube
SE_38638chr13:99127244-99131850HUVEC
SE_45616chr13:99127310-99132615Osteoblasts
SE_65772chr13:99126270-99131228Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr139913057199130717
Number: 1             
IDChromosomeStartEnd
GH13I098475chr139912765699131531
Enhancer Sequence
ATTAGAGTCG GGTCCCATCT CCCATCTCCT CCTTCACCAA GTCTGTGCCC AAGCCGACGA 60
TCAATACCTG TGGTTAGATC TGGACTTAAC CACCTCCCTT CCATTACCAA GTCTCCCAAA 120
AGCAACGGCA GAGCGGCCTG CTGTCATTCC CAAAGGGCGC TAAGAGGAAG AGGTGAGGAA 180
CACTCATGGA AAATCCTCCC CTGGATAATT AAGGGCTGGC TCTGTGATGA CTGTCTGCAT 240
GGTTCTGCCC TTTTAAATCT GCCCTGAACA CCATCCATCA TTGACTTATA TGCCCATGGG 300
GAACGAGGAG GAAGGGGAGA AAAAGAGATA AAACTCTCCT TACTTGGGGG GAAATCCTTT 360
CTGCGTCAAA ATTCACTATA AAGGGTATTC GGCTGCTGTC TACCCCCCAG AGTGCCTCAT 420
GAGCAGCTCG GACCAGGCCA AGCTCTCCAA GTCAGCAGCT GGTGTTCGCC ATTGCGACCA 480
TGCTCTCCAT CATTCAGGCA CTTGCAGACT CTTCAAATAG GACCCAGGAA AAAAACCTAG 540
ACCACATCCC ACCTCTGTGT GACTTCTAAC TCCCCCTCCC CGAGCCTGTC CTCCCCTGCT 600
TCGAAGCTCT GTAACAGGGA CTATTGGCCG GGGCACTCAG CCACAACAAG AAACCACATT 660
TCCCAGACTC TGAGCAGCAG CCTGTGGTCA GGTGACTAAG ACCTCGCCAG TGGGTCAGAC 720
AGGAGCAAAT GTGCCCCATG CCCCTGCTTG GTCTTGGCCC TGAAGCACTG GCAGTGGGAG 780
AGGACAATGG CTGAAGACCA AGGGAAGCCT GGGGCTCCAG ATGCTGAAGC CACCCACCAG 840
CACAGACCGT GACGGTATGG ACCAGAGCCA CTGACCCCAT GTGCAGGGGG AGAAATAAAT 900
TTCTATCTTT TGTGAGACAC TGTTTTAGAG CTGCTATGAT GGCAACTTGG CCTAAACATT 960
AATGAATATG CCATCTCATT TCTTAAAACC CATGTCGTGT ACTCATTTTT TAAGTCCGTC 1020
AAACATCTCT GCCTGATTAA GTGACTGGTT TATGTAGCAT TGTCCCTTTG TAATTAGATT 1080
CCAAGGTTGT CCCTCGGATT CTCTGGCAAC ACTGGCTGAT CTTTTAATCA GCTAAAACCT 1140
TCTGGTCTCA GGCCCTCTGT GGCTCATCCT CACTCCAGCT CCCCCATTCA CCTCCCTCGC 1200
CTGCATTGTT TTCCTTGTAA GGAAGGAACC TTCTAACAAA CGGTGTAATT GACAGACCTC 1260
CCCACCAGAA CTCCCCAAGA GCAGGACTTT CCGCTGCTGT GTCCAACGGC AATAATCCCC 1320
AATGGCCAGA GCAGCCCCTG ACACGCGGGA GGCACACAAC TCTATGCTGA ATGAAAAATG 1380
GTTTCCCTCC CCGGGCTACA AAGACAGACT GCATTTAAGT TAGGGTGTCT TGGACTGTGT 1440
GATACTTCTT ATGCTCTTCT AAGTCAGGGC ACCCTACAGG CAAGGCGGCT GGAACTTGAG 1500
AGATGACTGA CTTGAGTAGT TTTCAAGCTA TATTCCAAGA GCCCAGCGGC CTTGGGATCA 1560