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

TagContent
EnhancerAtlas ID
HS131-03380 
Organism
Homo sapiens 
Tissue/cell
ME-1 
Coordinate
chr16:31139730-31141330 
Target genes
Number: 40             
NameEnsembl ID
ZNF747ENSG00000169955
AC002310.13ENSG00000260869
PRR14ENSG00000156858
SRCAPENSG00000080603
RP11ENSG00000261840
U6ENSG00000222287
SNORA30ENSG00000206755
RNF40ENSG00000103549
C16orf93ENSG00000196118
ZNF629ENSG00000102870
MIR4519ENSG00000260083
BCL7CENSG00000099385
AC106782.20ENSG00000262721
CTF2PENSG00000230447
FBXL19ENSG00000099364
AC135048.13ENSG00000261487
ORAI3ENSG00000175938
SETD1AENSG00000099381
HSD3B7ENSG00000099377
STX1BENSG00000099365
STX4ENSG00000103496
AC135050.1ENSG00000232748
AC135050.5ENSG00000261124
ZNF668ENSG00000167394
ZNF646ENSG00000167395
PRSS53ENSG00000151006
VKORC1ENSG00000167397
BCKDKENSG00000103507
AC135050.2ENSG00000252809
KAT8ENSG00000103510
PRSS8ENSG00000052344
PRSS36ENSG00000178226
FUSENSG00000089280
AC106782.18ENSG00000261359
PYCARDENSG00000103490
TRIM72ENSG00000177238
ITGAMENSG00000169896
ITGAXENSG00000140678
ARMC5ENSG00000140691
CSDAP1ENSG00000261614
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
TFAP2AMA0003.3chr16:31140022-31140033TGCCTGAGGCT-6.32
Number of super-enhancer constituents: 13             
IDCoordinateTissue/cell
SE_09570chr16:31136894-31142959CD14
SE_23399chr16:31136970-31147903Colon_Crypt_1
SE_26229chr16:31138363-31143442Duodenum_Smooth_Muscle
SE_26836chr16:31138704-31147551Esophagus
SE_28070chr16:31138712-31147681Fetal_Intestine
SE_29017chr16:31138749-31148013Fetal_Intestine_Large
SE_31607chr16:31136963-31147939Gastric
SE_41880chr16:31139957-31144351LNCaP
SE_47601chr16:31139783-31143344Pancreas
SE_50623chr16:31137728-31147935Sigmoid_Colon
SE_52791chr16:31138165-31147634Small_Intestine
SE_58057chr16:31140484-31144007VACO_9m
SE_68934chr16:31140565-31147890H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr163113982831141058
chr163114000031140600
chr163113998931140736
Enhancer Sequence
TGGTGCGCAC CTGTAATCCC AGCTACTCGG GAGGCTGAGG CACAAGAATT GCTTGAACCT 60
GGGAGGCAGA GGTTGCAGTG AGCTGAGATT GTGCCACTGT ACTCCAGCCT GGTCGTCAGA 120
TTGAGAATCT GTCTCAAAAA AAAAAAAGAA GGCCTCTGAG GGCCTCCTAG CCTGGCACTA 180
GGCCTGTAGT TGGTGCATAG GAAACACAGG GCCTTGTGGT GGCCCCAAGA CTCTTCTGCT 240
GGTGGGGTTA GGTTCAAACT TGGGTTGTTC TGGAACCCAG AGGAGATTTT CTTGCCTGAG 300
GCTGCTTTTA GAAGTGCTCT CTCCTTCCGT TGGAAAGAAA GGTGTTTGTT TTTGCCTGGG 360
AGGGGACTGC TTTGTGTGAA ATTTCCTCCT GAGAGAGCTC TGTGGCTTTC AAGGTTTGAG 420
TTCCTTGTTC CTGGCCCCGA ATGACTTCAG CAGGGCAGGT TGGGGCCTTT GGGACCTGCC 480
TAGCTGTTGT AGAGAACTTG GCCTTTGCCT TATCAGTCTG GGAGGGTCTG GCCAAGTGTA 540
CTGGTTTCCC GCAGATGGGC CATACAGCAC AGGACAGAGA GGGCAGGCTT CAGGGTGGCT 600
CATGTTGCCT TGTCACTTCC TCACTGACCA CAGACAAGTT ACTTAACATG GTTTGTTCCT 660
GTTTCCTTGT CCATAAGACG GGAGTCATAA TATTTAATAT TTACCTAGTT GTGTTGTTAG 720
TGGAATAAAT GAGACAGCAA ATGTCAAGTG TTTAGTGCAG TGCTTAGCAC TAGTATGTGC 780
TTAATAAACA CGGGCCTTGT TATTATCGGT GACCTCTTGG GGCTTGATTA GCCTTGGACT 840
CGGAGAATAC GCAGGCTGAG CCCAGCCCTT GCCCCTGCTC TGCCTTCCTG AGCATGGCTG 900
TGTGGAATAG CAGAAGGGCC CCCGCTGGAG ATGTGGGGGT GCTTTCCAAC TGCGCTCTGC 960
CAGCTTTGAG GCTCTGGGCA AGCACTTCCA CTCTGGGAGC TTCAGCTTCC TCCTGAGTAA 1020
GATGGGCCTG GCAGTGCTGG GCTCGCACAG CTGCCGGGTT GGATGAGAGA GTGGCTGTGG 1080
TGTCATAAAC CAGGGAGCCC CTTAGTGTGT GCCGTGAAGC CAAACTCGGT CCCATTGTCC 1140
CCCTCCTGGA GTGCAGCCAA GTGGACAGAC AGGGCTCGAG GTTCCTCCAT TCAGCAGACG 1200
TTTACCAGGC ACCCAGCTTC ATACTTAGAC TCGTGCTAGG CGCTGGGGAC ACAGCCATGA 1260
ACAGGACGGT CTAAATTCCT GCCTCGGAGC CTCAGTTTCA CGAGCTGAAA CAGAGTTAAT 1320
GTCTGTGAAG ACTGAAGCAG ATCCTGCATG GAAGGCACCC AGCTCGTATT TGGCACTCAG 1380
AAGGGGTGGC CGGGCTTCAT CCAGCTCCAC TGGCACCTCC GAAGTGCTGT TGCTCTCTCA 1440
TTTCCAGTTC CCTGTTCGTC AGAGGCTGAC CGAAGACTCC TTCCAGTGTG AAATCCTTCT 1500
GGCCTGGCGA GGCGCCCACT TCGCGTGGGC TGGTGCCGGC CGCTGGAACC AGCTGGGTGG 1560
GGCCTGTGCC TGCCCCCTGA GCCTGTCTCC CCCCTCCTCA 1600