EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS101-46584 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr9:139690920-139693550 
Target genes
Number: 57             
NameEnsembl ID
DNLZENSG00000213221
CARD9ENSG00000187796
SNAPC4ENSG00000165684
SDCCAG3ENSG00000165689
PMPCAENSG00000165688
INPP5EENSG00000148384
SEC16AENSG00000148396
C9orf163ENSG00000196366
RP11ENSG00000227512
NOTCH1ENSG00000148400
EGFL7ENSG00000172889
AGPAT2ENSG00000169692
FAM69BENSG00000165716
SNHG7ENSG00000233016
TMEM141ENSG00000244187
KIAA1984ENSG00000213213
C9orf86ENSG00000196642
NCLP1ENSG00000213212
C9orf172ENSG00000232434
PHPT1ENSG00000054148
MAMDC4ENSG00000177943
EDF1ENSG00000107223
TRAF2ENSG00000127191
FBXW5ENSG00000159069
C8GENSG00000176919
LCN12ENSG00000184925
C9orf142ENSG00000148362
CLIC3ENSG00000169583
ABCA2ENSG00000107331
NPDC1ENSG00000107281
ENTPD2ENSG00000054179
SAPCD2ENSG00000186193
UAP1L1ENSG00000197355
MAN1B1ENSG00000177239
DPP7ENSG00000176978
GRIN1ENSG00000176884
LRRC26ENSG00000184709
ANAPC2ENSG00000176248
SSNA1ENSG00000176101
TPRNENSG00000176058
TMEM203ENSG00000187713
NDOR1ENSG00000188566
RNF208ENSG00000212864
C9orf169ENSG00000197191
RNF224ENSG00000233198
TUBB4BENSG00000188229
FAM166AENSG00000188163
COBRA1ENSG00000188986
C9orf167ENSG00000198113
NRARPENSG00000198435
EXD3ENSG00000187609
NOXA1ENSG00000188747
ENTPD8ENSG00000188833
NELFENSG00000165802
WDR85ENSG00000148399
C9orf37ENSG00000203993
SETP5ENSG00000233998
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MyogMA0500.1chr9:139693365-139693376GACAGCTGCTG+6.14
SCRT1MA0743.1chr9:139691734-139691749CACCACCTGTTGCCC-6.22
Tcf12MA0521.1chr9:139693365-139693376GACAGCTGCTG+6.02
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_23713chr9:139692982-139695833Colon_Crypt_1
SE_24285chr9:139693125-139694645Colon_Crypt_2
SE_25098chr9:139693022-139695891Colon_Crypt_3
SE_27891chr9:139683804-139691326Fetal_Intestine
SE_27891chr9:139691868-139692580Fetal_Intestine
SE_27891chr9:139692750-139696022Fetal_Intestine
SE_29352chr9:139685639-139691669Fetal_Intestine_Large
SE_41726chr9:139693034-139695890LNCaP
Enhancer Sequence
TGAGCCTGCA CCGCCGTGAC CAGTCTCCCT TTCCCGTCTG GGGGTTTCTG GGTGCACAAC 60
TTTTTGTGGG GAAAAGAGAG ATCAGATTGT TACTGTCTAT GTAGAAAAGG AAGACATAAG 120
AAACTCCATT TTGATCTGTA CTAAGAAAAA TTGTTTCTGC TTTGAGATGC TATTAACCTG 180
TAACTTTAGC CCCAACTCTG TGCTCACAGA AACATGTGCT GTATTGAATC AAAGATTAAT 240
GCATTTAGGG CCGTGCAGGA TGTGCTTTGT TAACAATGTG TTTGCAGGCA GTATGCTTGG 300
TAAAAGTCAT CCCCATCCTC CATTCTTGAT TAACCAGGGA CACAGTGCAC TGCAGAAAGC 360
CGCAGGGACC TCTGCCCAGG AAAGCCTGGG AATTGTCCAA GGTTTCCCCC CACTGAGACA 420
GCCTGAGATA TGGCCTCGTG GGAAAGGAAA GATCTTACCA TCCCCCAGCC CGACACCAGT 480
AAAGGGTCTG TGCTGAGGAG TAGTGAAAGA GGGAGGCCTC TTTGCAGTTG AGATAAGAGG 540
AAGGCATCTG TCTCCTGCTC GTCCCTGGGA ATGGAATGTC TCAGTGTAAA GCCGACCATT 600
CCCATTCGTT CTATTCTAAG ATAGGAGAAA ACCGCTCTGT GGCTAGAGGC AAGATATGCT 660
GGCAGCAATA CTGCTCTGTT ACTCTTTGCT ACACTGAGAT GTTTGTGTAA CGTGAAACAA 720
ATCTGGCCTA CGTGCACATC TGGGCATAGT ACCTTTCCTT GAACTTATTC ATGATAAAGA 780
TTCCTTTGCT CACATGTTTC CCTGCTGACG TTCTCACCAC CTGTTGCCCT GCTACACTCC 840
CCTCACCAAG ATAGTAAAAA TAATGATCAG TAAATACTGA GGGAACTCAG AGACCAGGGC 900
TGGTGCAGGT CCTCGCATGC TGAGTGTGCC AGTCCCCTGG GCCCACTGTT CTTTCTCTAT 960
ACTTTGTGTC TTTTTTTTTT TTTTTTATGA GATGGAGTCT TGCTCTGTTG CCCAGACGGC 1020
AGTGCAGTGG CGCGATCTCG GCTCACTGCA AGCTCCACCT CCTGGGTTCA CGTCATTCTC 1080
CTGCCTCAGC CTCCCAAGTA GCTGGGACTA CAGGCACCCA CCACCATGCC CGGCTAATTT 1140
TTTGTATTTT TAGTAGAGAT GCGGTTTCAC CGTGTTAGCC AGGATGGTCT CGATCACCTG 1200
ACCTCGTGAT CTGCCCGCAT CAGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCA 1260
TGCCCAGCCT CTGTGTCTTA TTTCTTTTCT CAGTCTTCAT CCCACCTGAC GAGAAATACC 1320
CGCAGGTGTG GAGGGGCAGG CCCCCTTCAC TTTTAGGGGA TGTTTGTTTG GAGACAGAGT 1380
CTCGCTCTGT CACGCAGGCT CGAGTGCAGT GGCATGATCT CGGCTCACTG CAACCTCCAC 1440
CTCCCGGGTT CGAGCGATTC TCCTGGCTCA GCCTCTTGAT TAGTTGGGAC ATCAGGTGTA 1500
CGCCACCACA CTCAGCTAAT TTTCGTATTT GTATTTTTAT TTATTTATTT ATTTTGAGAC 1560
GCAGTCTCGC TCTGTCACCC AGGCTGGAGT GCAATGGTGC AATCTCAGCA CACTGCAACC 1620
TCCACCTCCC GGGTTCAAGT GATTCTCCTG CCTCAGCCTC CCGAGTAGCT GGGATTACAG 1680
GTGCCCACCA CCACGCCCAG CTAATTTTTG TATTTTTAGT AGAGACGGGG TTTACCCATC 1740
TTGGCCAGGC TGGTCTCAAA CTCCTGACCT CAGGTGATCC ATCCGCCTCG GCCTCCCAAA 1800
GTGCTGGGAT TACAGGCATG AGCCACCGGC GCCTAGCTTA TTTATTTTTT TGAGACAGAG 1860
TCTCATTCTG TCGTCCAGGT GGAGTGCAGT GGTGCAATCT CAGCTCACTG CAACCTCCAC 1920
CTCCTGGGTT CAAACAATTC TGCCTCAGCC TCCTGAGTAG CTGGGACTAC AGGCACACAC 1980
CACCACACCC AGCTAGTTTT GTATTTTTAG TAGAGATGGG GTTTCACCAT GTTGGCCAGG 2040
CTGGTCTCGA ACTCCTGACC ACAGGTGATC CGCCCACTTC GGCCTCCCAA AGTGCTGGGA 2100
TTACAGGTGT GAGCCACCGC TCCTGGCCTA GGACTTTTAG TTTTAATACA GGGACAATCC 2160
AGGACATGGA GGGGAAAACA GACCCCCCTA CTGCCCACTC CCTGACAGAG CTGGGAGAAG 2220
GGATCAAAGG GACCTGCATG GAGGGACTAA ATCAGAGAGA GGGGCTTCAA GGAGACGTGA 2280
GCATAAGAGC AACACGGGCC CCAAAGCCAG AATGGACAGG AAAACACCCA CCTGCTTCCA 2340
TGGGCAGCAA ATCTGGACGG GACCACAGGA CCCTGCCATC CCTCTCCTTT GCCTCACCCT 2400
CCCCACCTGT CCACCTCCCC GCACCTGTCC ACTGAGAGCC CTTCAGACAG CTGCTGCTGG 2460
GCAGTGGAGC GGTGTCCCCC AGGACAGGGC GGGAGGAGGG ATCTTGGCCA TGGAGGGGGC 2520
ATCCCCCTGG ACCCTGGGGC CTGGGGCCTC CCTGATGCAA GCCTCCCCCA GGGGATTCCA 2580
GGCCAGGCCC TTGGCCCAAT CCTAGCCACT GTGTCCCCTC CACCTGCCCA 2630