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

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EnhancerAtlas ID
HS048-37382 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr9:92213140-92214490 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1007966chr992213967hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
OLIG2MA0678.1chr9:92214168-92214178ACCATATGGT+6.02
OLIG2MA0678.1chr9:92214168-92214178ACCATATGGT-6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr99221387892214234
Number: 1             
IDChromosomeStartEnd
GH09I089598chr99221312192213290
Enhancer Sequence
CTGGAAGGGT TTAGGCCAGC TGAGGTGTTA GAAGCTACTT TTTAGGGCTG GAAGCGATAT 60
TCTCTTTGAC CGCAAGATGT CACCCTGCAA CCATGACATT GGGACAGGCA CTGTTGGATT 120
CAGGGTTCCT GAGGAGAACC AAAAATGGTT TTGAAACCTC ATTTTCACCT GGATGCTCTC 180
CTTGTCCTTG GTGGTCAAAT GGTTTGTTCT AAAGGCTCGA GAAATGGTTT CACAGTGAAA 240
TTCATCTGTT CCCTCTTGCT TCAGAGAGGA GCTCAGAACA CCCAGCTTTG CCACCTCCTG 300
GCTGTGTGAC CTTGAGCAAG TTGTTCAACC TCTCTGTGCC CAAGATTCCT CATGCCTAAA 360
ATGGTGATAA TAGCACCTAC ATAACGAGTT TGTTATGAGA ATTAAACAAT GTTTTCAAAG 420
TGCTTGGAAC AGTGCTTGGT GCACAGCAAG TCCTGGAAAA GTCTAGTAAA TAAAATAACA 480
ACAATACTAC TAATAGTGTA CTCAAGGAGT GCCACACCCT TCTCAAACAG ACAAAATTCA 540
AACACTGAAA AATTAAATAA TACCCTACAG TCTCAAGCAC AGGTTGAGTA TATTACATGT 600
TTTGAAATTT TAGAATTCCC TGCTGTGTTA TGTAGGCAAT GGAAACAATT TTCATAATCT 660
ATTACTGTAA TTCATTTCTG GAAAACAGAC ATTTTCAACA AGAAGGGAGT GGAAGATAAT 720
TTCTTCCATT GCTGCTTGCC TCAGTGTGCG CAGAGGATCC CCAAGGGTCC TGTGAACCGC 780
ATTTGTAAGG AAAGGTGCCG TCCAGGGTGT TTGGTTCTGA CTTGCCGGCT GGCCTTCTTT 840
CCTGCCTCCA GCATGTTGCC TGGGATTCCA TCCCAGTCAT GCCAGAGTTA ACCTCCGAGT 900
ACAGTTATGA CGATTTTCAC TCAGTCACAG GCGCAGACCG GCGTCAGATG GCAAGAGGAG 960
GAGTGCAGGA ATCAAAGGTC ACAGTCTCAG GAGCAAAGCC CCACAGACGT CTGGCTTCTG 1020
GATCTGTGAC CATATGGTCA AAGATTGCTC TGCACAATAA CCTCCAGAGC AGTCAGGTTG 1080
AGGATGTCTG GTACTGAAGT TACTCCATTT GAGAAGTTTT ATATATTTTT GTTAAATAAA 1140
ATTGAATTGT AAATGTTTAA TTGCAGTAAA GCATAGTGAA GAAAATTAAA AATCACTTAT 1200
AATCTCATCA CTCCAAGATA CAATCACCAT TCCTACTTTG TGACTTTATA CAGTGATAGT 1260
CGTGTACGCT GAAAGTTTTT GCAAAATTAG AATTGCACAA TTTCGTATTT TGCTTTTTTT 1320
CACATTATAT CATGCCGGGA ACTACTCTTC 1350