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

TagContent
EnhancerAtlas ID
HS091-17093 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr16:31144710-31146470 
Target genes
Number: 48             
NameEnsembl ID
ZNF768ENSG00000169957
AC002310.17ENSG00000261588
ZNF689ENSG00000156853
RP11ENSG00000260113
FBRSENSG00000156860
SNORA30ENSG00000206755
PHKG2ENSG00000156873
RNF40ENSG00000103549
C16orf93ENSG00000196118
ZNF629ENSG00000102870
MIR4519ENSG00000260083
MIR762ENSG00000211591
BCL7CENSG00000099385
AC106782.20ENSG00000262721
CTF1ENSG00000150281
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
ITGAMENSG00000169896
ITGAXENSG00000140678
ZNF843ENSG00000176723
ARMC5ENSG00000140691
TGFB1I1ENSG00000140682
SLC5A2ENSG00000140675
AC026471.6ENSG00000260740
C16orf58ENSG00000140688
CTDENSG00000261741
CSDAP1ENSG00000261614
ZNF720P1ENSG00000260010
KIAA0664L3ENSG00000131797
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr16:31146433-31146454CACCTCCCCCTCCCCTCCTCC-6.79
ZNF263MA0528.1chr16:31146436-31146457CTCCCCCTCCCCTCCTCCCTC-7.65
Number of super-enhancer constituents: 14             
IDCoordinateTissue/cell
SE_09570chr16:31144747-31146697CD14
SE_23399chr16:31136970-31147903Colon_Crypt_1
SE_26229chr16:31144701-31147451Duodenum_Smooth_Muscle
SE_26836chr16:31138704-31147551Esophagus
SE_28070chr16:31138712-31147681Fetal_Intestine
SE_29017chr16:31138749-31148013Fetal_Intestine_Large
SE_31607chr16:31136963-31147939Gastric
SE_41880chr16:31146016-31147661LNCaP
SE_47601chr16:31144441-31147878Pancreas
SE_50623chr16:31137728-31147935Sigmoid_Colon
SE_52791chr16:31138165-31147634Small_Intestine
SE_57031chr16:31145964-31147591VACO_400
SE_58057chr16:31145611-31147802VACO_9m
SE_68934chr16:31140565-31147890H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr163114489831145251
chr163114532731145800
Enhancer Sequence
TGCCCAGGGA GGAAGGGAAG GGGTCAGGTT GTTAGCCTGG CCACTCCTAT GCAGCCCAGG 60
AGCTCTGATA TAGAGCTTGG GAAGTGGGTT CACAGGAGTC AACACCCCTT TGTCCCCTCC 120
CAGGCATGGG CAGTTGTGCC CCTTCTGTCC ACTACCCATT ACCTAATTCA GGTCTCATGG 180
CAGCTTCTCT CCTTGCAAGC CTTCCATCCA TCCCGCCCCT TACAAGTCTG AAGATTTTCA 240
TAAACCCCCA ATCTGACCAG GCCACAGCCC TGCTTAAACC CTTCTTGGCT CCACGCGGTC 300
CTTAAGATAC ATTCCAGACA GACCATGGCA CCGCCATCGG ACCCAGCCGT CCCCTCTGGA 360
CCCTTCAGTT GTGTACATCA GGCCACACAC TTGTTTACCC GGGACCTTGG CTGATCCAGG 420
TCACTCTACC TGGTATGCCC TTCCCCATCC TTACTGTCTG GCAAACTTCC CTTTGCCTGT 480
GGATGCTTGA TTGGAACAGC AGCCCCTCCG TAGACAGGCG GGCTTCTGCT GGCTGAGTTG 540
GGCATTGCCT CCGAGCCCAG CACCCCCCAA CCTCCACCAT GCTCCCCGAT GCTGCCCAGT 600
CTCACAATTG TTCCGGAGTC CACAACTGTG TCTGTTTCCA CCACACCAAT CTGGGCATTC 660
CCTAGGGGCA GATTCTCATG TCTGCAGTGC CTGTGGCGTC GTGGACATAT ATTCAACAAA 720
CCAACAGCAG AACTGGGCTC CTGTGATGTG AATGTCTAGT TTCCAGGACA GCCCCAGCCC 780
CACCCCCATT GAGGCCACTT TGGAGTGGAG CCCAACTGCT CTTCACAAAG TCATCTAGGA 840
GCAGAGAAAA TTGCAGACCA GATCTTTCTC TCCCTTATCA TCATGACAAT AGCCACTATT 900
TAGAGAGCCT AGCGGCTGTG CCAGGCCCTG GAGGGGCTTT CGCTTCCTCA TCTCCCTGCA 960
TCCTCTCCAC AGCCCCAGGA GACGGACATG ACCAGCTTCA TTTTAGAGGT GAGGAGTCTA 1020
AGGCTTAGAG AAGTGGGGGG ACTTGGCCAA TGACACACAG CCAGTGCATG GGGAAGCCAG 1080
GATTGAAAGC CGGTCTGACT CAGAGCTGGG TTGGGTGCCT TCCAAGAAAG GAGACCCTTG 1140
GTTTGGTTCC CTCAAAACCA CCTCCAGGAT GGGAACGGTG GCTCACACCT GTAATCCCAG 1200
CACTTTGAGA GGCCAAGGCA GGAGGATCGC TTGAGCCCAG GAGTTCAAGA CCTGCCCGGC 1260
CAACATAGTG AGACCCACAT CTCTACCAAA CAAAAACAAA AACAAAAACA AAACACAACT 1320
AGCTGGGTGT GATGGCATGC ACCTGTAGTC CCAGCCACTA GGGAGGCTGA GGTGGGGAGG 1380
TGGGAGGATC ACGTGAGCCC GGGAGGCTGG ATCACTGAGA CTGCAGTGAG CTGCGATCGG 1440
GCCACTGCAC TCCAGCCTGG GTGACGACAG ACCCAGACCC TGTTTCAAAA GACAAAAACC 1500
AAACCAAAAA AACCACCTCG ATTGCCCCAC TTTGGGAGTC AGACGTGGAT CTGAATCCCA 1560
GCTGCACCTT CACTGGCAGT GTGCCCTGGG CAAGTCCCTG CTTCTCTGCC CATAAGGTGA 1620
GGGCTAAAAC CCCCCACTCT GGGAGCCCTA AGAGAATCTA GTTGGAAGGC AGCCCAGCTG 1680
AAGGCCAGGC ACTGGTTAAA CCCCAGGGGA ATCCGATCCA AGTCACCTCC CCCTCCCCTC 1740
CTCCCTCTCC GAGGAAAGTC 1760