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

TagContent
EnhancerAtlas ID
HS098-13369 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr12:57525480-57528470 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11172113chr1257527283hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr12:57526979-57526999TGTGTGTGGCTGGGGTGGGG-6.39
RREB1MA0073.1chr12:57527408-57527428CCCCACCCCACCCCCCGCAC+6.72
SPI1MA0080.4chr12:57526738-57526752GACTTCCTCTTTCT-6.21
SPICMA0687.1chr12:57526738-57526752GACTTCCTCTTTCT-6.67
ZNF263MA0528.1chr12:57526746-57526767CTTTCTTCTTCCCCCTCCACT-6.32
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_00100chr12:57519878-57554240Adipose_Nuclei
SE_01991chr12:57520288-57527431Aorta
SE_01991chr12:57527432-57528492Aorta
SE_04195chr12:57522419-57530997Brain_Anterior_Caudate
SE_05741chr12:57520316-57528205Brain_Cingulate_Gyrus
SE_06171chr12:57520260-57534210Brain_Hippocampus_Middle
SE_07493chr12:57520887-57533823Brain_Hippocampus_Middle_150
SE_07952chr12:57522404-57531077Brain_Inferior_Temporal_Lobe
SE_26173chr12:57522851-57530891Duodenum_Smooth_Muscle
SE_26822chr12:57525442-57528474Esophagus
SE_28331chr12:57526015-57527317Fetal_Intestine
SE_30586chr12:57525262-57528366Fetal_Muscle
SE_39018chr12:57520767-57527336IMR90
SE_44332chr12:57522407-57528487NHDF-Ad
SE_45184chr12:57525333-57528483NHLF
SE_46164chr12:57522434-57531208Osteoblasts
SE_46749chr12:57526044-57526519Ovary
SE_46749chr12:57526576-57527375Ovary
SE_46749chr12:57527459-57528226Ovary
SE_49434chr12:57522392-57528504Right_Atrium
SE_50286chr12:57520201-57528600Sigmoid_Colon
SE_52937chr12:57525285-57527386Small_Intestine
SE_52937chr12:57527412-57528434Small_Intestine
SE_55833chr12:57520023-57528498u87
SE_67616chr12:57520023-57528498u87
SE_68957chr12:57526846-57528260H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 7             
ChromosomeStartEnd
chr125752658657527444
chr125752813057528213
chr125752621257526408
chr125752660057527000
chr125752700057527302
chr125752780057528275
chr125752579957526525
Enhancer Sequence
TTTTGATGTT TAGGGCTGCT TCACTAGACA TCTTTTTCTT CTGATCTTGT TCTCTCTCCT 60
CTCTTCATTT TCTCAACCAC CCTTCCACCA CTGAGCCTCC CAAAGGATGA CAGCCCAGGT 120
CCTGGCCAGA GTCAGTTCCT GTCCAGATGC CCCCATTCTT CAAAACCCCT TCCTTACCTT 180
TTGGGAAGCC CTTCCTTACT CAAGTCTATC TCTCTTTCCT CCTGCTGCAG TGTGAGCCCT 240
TGCACATCAG AACCCCCAAG CCTAGGTTTA TTCCCGCCCA GTACTCTCTT CTCAGGGTCC 300
TCCTCACTCC TCAGACTCTT TACCTTTCAG GTCCTCCAGC TCTGCGTGTG GGCTCATTGC 360
TCTTGGGGCA TCTGGGTGCA GCTGAATGGT ACTGCAGGAA GGCCCCTGAC TTGGTAGTGC 420
TGGGTATGAG CGATAGAGAA CCTGCCTCCC TCTTCTGTCC CAGATTTCAG CCTGGTTAGC 480
AGGATCCTGC ATTGTTTGGA GAAGGAAGCA GTTGGCTTTG GAGTGTTTCC GGTGCAATGG 540
CCTCAGGCAC CAATATAAAC CCTCCCTGGG AAAGAGGTGA GGGGTATATG TGGAGAGTTG 600
TCCCTCTTGC TCCCCTAGGG GAGATGAAAG CCTCTCCCTC TCCCACCAGG CCTTAGCTTC 660
CCTGGCTGAA GAGCTCCATT TTCCTCCCTC CTTTCTACCC TCCTGACTCC AGGGGTGGTA 720
GTGGTCCCTA TTCTGGGTCT CCCTTGAGTC AGGCACTGCC TAGGGCCGAG ACTCTGTCTC 780
TCCAAGATAG GACAGATCTT GCTCCCACCC TACTCTAGGC TCAGCGGGGT AGTCATTCTC 840
TGGGTTCATC CCAGGACAAC TGTGTCATCC CCTTGGCAAT CTCTGGACTG AGCCCCCTTC 900
CTGGCTTTTC TGGCTGTCTG TCTGTCTTTC TGTCTGTCTG TCATTAGTGT GCGCTGTCTT 960
GGCTTTTTAG AACCTCTCTG TCTCTCACCC TCTCAGTTCA TCTCTTACTG CCGAACCTTT 1020
GTGACATTCT CTGCCCTGCT TTCTGCGTCT CTGTCACTTG TCTTATTTTT CTCTGCCTGT 1080
CTCCATTTAC CCCCATCCAG GCCTCTTGGT ATCCCAAAAG CTTCTTGGGA GCAAGAGTCT 1140
CTCTGGGCTT TCCCACTCAC CCCCTGGCTC CCTCCCCTCT GTTTTGGCTA TTTTTCCCCC 1200
TTCCTGGCCA GACCCAGTGT CCAGTTCAGC ACCAAAAGTT TCCTCTCCAC TTTCCTCCGA 1260
CTTCCTCTTT CTTCTTCCCC CTCCACTAAT TTGGGGAATG GGTTTTGGAG AGAATGTTTC 1320
TGGAAGAAAG GAACTTGATA CCCTTTGTGG GCTAAGAGGG AGAAAGGAGG TATTTCAGAA 1380
GGAAGGAGGG AGGTTAGACT TCTGGCAGAA CTTCCTCCTG ACCAGGAGCC TAAGAACTGG 1440
AGAAAGATGT AAGGAGTGAG TCAAGAACTT GGAGCTTTTA CTCTGGTGAG CATAAGCTGT 1500
GTGTGTGGCT GGGGTGGGGG GAGAAGGAGA GGAGGCTTAG AAATGCCTGG TGAGTGATAT 1560
GGTGACCTCT GGAGGCCTTC TGGGGGTCTG GCTTTTATTT GTGGGGAAAG GAAAAGCTGG 1620
TGGGGGAGGT CACGGGTCAG GCTAATGTCC TGCTGCATCA ATATTGACTC AGAATGGAAG 1680
CGGAGACCCT TCCCCTCCCC TGGCTGTCCA AGCCACCCTG TCTGTCTGTC TGTCCAGGCC 1740
GCAAAGCAGA GGCCCAGACT CAGGAATGAC AAAAATGTGT CTGAGCCTCA GGAAAGAGCC 1800
ACTGGGCAAC ACCCAAAATA CAAAAAATTC AGTGAAAACC TCTCGGTTTG GGTTTGGGAG 1860
GCCCTTGCTG CCCCACCCCC ATAAGGTCGA AAATTCAGAT TCCTGCAGGC TCTGTCCCCG 1920
CGCCGCCCCC CCACCCCACC CCCCGCACCT TGAGCATCCT CCTCCCACTC TGTTCCCTTA 1980
GCTATATCAT GTGGTTCCCT TTAGAGAACC CCCCTCTCAC CTAGCTCAGA GGGGAGCCTA 2040
TCTCTCCTTC TGCTGTGTCC ACTCTTAAAA AGGGCCCCAA GAGTCCCTGT CATGCTTTTG 2100
CAGTCCCTGA GTCTCCTTGT CCTTTAAGAA GCACCTCTAA GGTCTTAGCT CTCTTCCTTG 2160
CTCTCGCTCC CTCAAGGGGG TATCAAAGGA TGGGTTCCCC TCCTCTGGAG AAGACTCCTT 2220
CAGGGTTGGA CTTCGCTGTC ACCCTCTCTG GCCAGGCATT CTCACCCCAC TTCCCCACCC 2280
CCAAGGTCCC AGAATGGGAC ACAGAATGAC AGCCAAGGGT CAAGCAGGGC AGTGGGGTCT 2340
GTGTTGTGTC TGGACGCACA CCCAACTCTA CACCTCCTGC CCTGGCTCCA GCTTGGTGGC 2400
CCTGGGGACC GTGGCTGGGC TGGGTGCCTG GGTTTGGGGG GGTGGGGCAG GGTGTTGGCC 2460
AAGTTAGCAT GGCAGTCACA TTCATCTTCA GGCAAAGCCG AGAACAGACG GCCCCTGTGT 2520
CCTGGTGTTC TTCCTCCAAA CTCGCTCTCT CTCCTTCCTC TCTAGATCTC TCCTTCTTCT 2580
TCTCCTGCCT GTCTTCCCCT TCTTCTGTCC CATTCTTGCT CCTCTCTGTC TCCCCTATGC 2640
CCTTCCCTCC TCTCTGAGGA GCCCTGAAGG CCACCCCTTA AAATCCTCTC CCCACTGCCA 2700
GGGCCAGAGA ACGACAGCGT TCTCCCTGCA ATTTCCCTTC CTTGTTTTTT GTTTTTGTTT 2760
TGTTTTGTTT TTGAGACACA GTCTCACTCC ATCACCCAGA CTGAAATGCA ATGGCGTGAT 2820
CTCTGCTCAC TGCGACCTCC GCCTCCTGCT AATTTTTGTA TTTTTAGTAG AGACAGGGTT 2880
TCACCATGTT GCCCAGGCTG GTCTCAAACT CTTGACCTCA AGTGATCCGC CCATCTCCGC 2940
CTCCACCTCC CAAAGTGCTG GTACTACAGA CGGGAGCCAC TGCGCCCATC 2990