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

TagContent
EnhancerAtlas ID
HS197-03801 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr11:62238380-62241360 
Target genes
Number: 43             
NameEnsembl ID
INCENPENSG00000149503
RP11ENSG00000236607
SCGB1D1ENSG00000168515
SCGB2A1ENSG00000124939
SCGB1D2ENSG00000124935
SCGB2A2ENSG00000110484
SCGB1D4ENSG00000197745
ASRGL1ENSG00000162174
RCC2P6ENSG00000254454
AHNAKENSG00000124942
EEF1GENSG00000254772
MIR3654ENSG00000255508
TUT1ENSG00000149016
MTA2ENSG00000149480
ROM1ENSG00000149489
EML3ENSG00000149499
B3GAT3ENSG00000149541
GANABENSG00000089597
INTS5ENSG00000185085
METTL12ENSG00000214756
C11orf83ENSG00000204922
C11orf48ENSG00000162194
UBXN1ENSG00000162191
LRRN4CLENSG00000177363
GNG3ENSG00000162188
BSCL2ENSG00000168000
HNRNPUL2ENSG00000214753
TTC9CENSG00000162222
ZBTB3ENSG00000185670
POLR2GENSG00000168002
TAF6LENSG00000162227
TMEM179BENSG00000185475
TMEM223ENSG00000168569
NXF1ENSG00000162231
STX5ENSG00000162236
WDR74ENSG00000133316
RNU2ENSG00000222328
SNORD29ENSG00000206653
SNORD22ENSG00000252140
SNHG1ENSG00000255717
SLC3A2ENSG00000168003
AP000438.2ENSG00000257002
CHRM1ENSG00000168539
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr11:62240286-62240297AGTGACTCATG+6.14
GCM1MA0646.1chr11:62239252-62239263GATGCGGGTAC+6.14
NFAT5MA0606.1chr11:62239026-62239036ATTTTCCATT+6.02
NFATC1MA0624.1chr11:62239026-62239036ATTTTCCATT+6.02
NFATC3MA0625.1chr11:62239026-62239036ATTTTCCATT+6.02
NFE2L1MA0089.2chr11:62240014-62240029ACTGATGAGTCATCA-6.02
Nr2f6(var.2)MA0728.1chr11:62238865-62238880TGAACTCCTGACCTC-6.22
Nr2f6(var.2)MA0728.1chr11:62240342-62240357GAGGTCAGGAGGTCA+7.19
RARAMA0729.1chr11:62240342-62240360GAGGTCAGGAGGTCAAGA+6.22
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_47222chr11:62238893-62240521Panc1
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr116223909262240650
Number: 1             
IDChromosomeStartEnd
GH11I062471chr116223905162241117
Enhancer Sequence
TGCTGGGCCT GTTCCAGTCC CCCGAGACCT GACCGTCCCT GCTGGACAAC TCAGATGCCT 60
CATCCACCTG GGGTCAACCC CTGCAAGCTG AAAGAACGTC AGATTTTATT TATACCAATA 120
CGAAAGAAGG CTTTGGGGAG AAACTTTTGT CAGGCAAGAG CTTCAGCCTC CTGCATCCAG 180
CTGCAGGGAT GATGGCCCAT GGGGAGGTGG CACACCTCAG AGGAGTCTTT TTCTGACTGC 240
AAACACAGTC CAAGCTACCC TGGAGCAGAG TTTCTTAATA GTGACGCCTT TGACATTTTG 300
GGCCAAAGGA TTCTTTGCTG TGGGAGGCCG TCCTGTATGT TGCAGGATGT TGAGGCTACT 360
AGGGGGGCTT TGGTTGTCGC AACTAGGGGG GGCTTCCACT GGCATCCAGT GGGCAGAAGG 420
CACGCCAGGC TAATTTTTGT ATTTTTAGTA GAGACGGAGT TTCGCCATGT TGGCCAGGCT 480
GGTCTTGAAC TCCTGACCTC AGGTGATCCG CCCACCTCAG CCTCCCAAAG TGCTGGGATT 540
ACAGGCATAA GCCACCATGC CTGACCAATT TTATACAATG TTTTAAATAA TTTTGTGCAT 600
TAAACAGAAT TTTGACTGTG ACCTGTCACA TGAGGTCAGG TGTGGAATTT TCCATTTGTG 660
GCATCATGTC AGCACTCAAA AAAGTTTGGG TTTTGGGACA TTTTGGATTT CGGATTTTTG 720
GATTAGGGAT GCTCAACCTG CACTATCACT GTACATGTTG CAAATGGGGA AGGTGAGGTT 780
CAGAGCCCAG TAAAGGCCTG CTTGGGGGCC AGGCAGCCCA TGGCAGGTGA AGCCGGACAT 840
GCCCTGAGGC CTGGGTGTGG GAGACTGGCC GGGATGCGGG TACCCACAGG CACCCCTCAG 900
CCCCGCACAC TGGCAGTTAG GAGAAAGAGA ATGGCAGAGA GAAAGGGATC TGAGAAAAGC 960
AAGAAGAGCA CAAATGAAGA AAGGGAGAGG TGAGATGGAC AGGGAGAGGG GTGGAGAGAT 1020
AGAGGAAGGC CCATCTGCCC AATCCCTGGG TGACTTAAGG GCTGCTACGA CCACTCGCCC 1080
CAGGGTCTGG GTCATCTCCC CTTGGAGCCA GGAGGCTGCC CATGACCCGG GTCCTCCTCA 1140
GGAGGAAGCA CGCACAGCCC CCTTGTTGAG GCAGAGGGCT GGCTCCGTAT CAGTCCTTCC 1200
CTGTGCCCAC AGGCCCCCTT TCCCACATCT CTGGCCTCCT TGCCTTCACT GACTTCCCAT 1260
GCCGTCACAC CACCTGCCTC TAGACCTAGA GTGGGCCCAG CCCCGGCCTC CACTTGGATT 1320
GACCTCTGTG GCTCTCACCC GACTCCTCTC ACCCTCTGTA GACCGCACAG CCAGACACCC 1380
ACCTGACCCA GACCCTCCCC ACTGCTGGCC TTCCTTTATC AGCTCCTTGC CTTCCCCTCT 1440
GACCCATGGC TCACTGACCC TCCCTGCATG GGCCAGTCCT CACAACTGTT CTTCTACTGT 1500
CCTTCCACTC TGAGTTCTTA GGCTTTTGTC AACACCCCAG CCCTCAGCAA TGCCTGCCAG 1560
AAACCACCCC AATCCCAAGG CCCCACTGTC ACCCTTACCC AAATCTCCTC CTTCCCGCCT 1620
CTCAGCCCAC ACTCACTGAT GAGTCATCAT CCAGCCCTCA CCATCCCTAT GAAGTCAACC 1680
CTCAAACCCT GTGCCAGGAC AGCACAGCCC CCACCCCCTG CCACCATCCT CTCCTATAAA 1740
TTCTCAAAGA ATGGTCCAGA CTCCTACATG AGAACTACCA GGGCCCTTTG CTTAAAATAC 1800
TGTGACAGTG AAATAAGCCA GACACAAAAA GACAAATGCT GTATAACTCC ACTTATCTGA 1860
GGTACCTGCA GTAGTAAAAT TCACGAAACA AAGTAGGGCT AGGTGCAGTG ACTCATGCCT 1920
GTAATCCCAG CAATTTGAGA GGCCAAGGCG GGTGGATCGC TTGAGGTCAG GAGGTCAAGA 1980
CCAGCCTGGC CAACATAGTG AAAACTTGTC TCTACTAAAA ATACAAAAAT TAGCCGAAAC 2040
AGTGGTGCAT GCCTGTAACC CAGCTACTCG GGAGGCTGAG GCACAAGAAT CACTTGAACC 2100
CAGGAGGCAG AGGTTGCAGT GAGCCAAGTT CACACCACTA TACTCCACCC TGGGCAACAG 2160
AGCAAGACTC CATCTCAAAA AAAAAAAAAA AAAAAAAAAA AAAAAAGGCC AGGTGCGGTG 2220
GCTCATGTCT GTAATCCCAA CAGTTTGGGA AGCCAAAGCG GGTGGATCAC AAGGTCAGGA 2280
GTTCGAGACC AGCCTGGTCA ACATGGTGAA ACCCTGTCTC TACTAAAGAC ACAAAAAAAT 2340
TAGCCGGGCA TGGTGGCGGG CACCTGTAAT CCCAGCTACT TGAGGGGCTG AGGCAGGAGA 2400
ATCGCTTGAA CTCAGAGGTT GCAGTGAGCC GAGATCATGC CATTGCACTC CAGCTTGGGC 2460
AAAAGGTCGA GACTCCATCT AAAAAAAAAA AAAAAAAAAA AAAAAGGCTG GGTGCGGTGG 2520
CTCACGCCTG TAATCCCAGC ACTTTGGGAG GCCAAGGCGG GTGGACCACA AGGTCAGGAG 2580
ATCGAGACCA AGGTGAAACC CCGTCTCTCC TAAAAATACA AAAACAATTA GTCGGGCGTG 2640
GTGGCAGGCG CCTGTAGTCC CAGTTACTCA GGAGGCTGAG ACAGGAGACT GGCGTGAACC 2700
TGGGAGGCAG AGCTTGCAGT GAGCCAAGTT TGTGTCACTG CACTCCAGCC TGGGCGACAG 2760
AGCAAGACTC CGTCTCAAAA AAAAAAAAGC TGTATAAAAC AATGATAGGA ACCAGGCTCA 2820
GGTCACGCTA TAATCCCAGC ACTTTAGGAG GCTGAGGCTG GAGGATTGCT TGAGCCCAGG 2880
AGTTCCAGAC CAGCCTGGAC AACATGGTGA GACCCCCACC TCTACAAAAA AAATAAACAA 2940
AATTAGCTGG ACATGGTGAT GTGTGCCTGT AGTCTCAGCT 2980