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

TagContent
EnhancerAtlas ID
HS180-00997 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:27470550-27473240 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr1:27472624-27472635GGATGACTCAG+6.32
GATA2MA0036.3chr1:27471198-27471209ACAGATAAGAA-6.14
Gata1MA0035.3chr1:27471198-27471209ACAGATAAGAA-6.62
IRF1MA0050.2chr1:27471570-27471591AAAAAAAAAAAGAAAGTGAAC-6.86
JUNBMA0490.1chr1:27472624-27472635GGATGACTCAG+6.14
PHOX2AMA0713.1chr1:27470758-27470769TAATTCAATTA+6.14
Phox2bMA0681.1chr1:27470758-27470769TAATTCAATTA+6.14
ZEB1MA0103.3chr1:27472695-27472706GGGCAGGTGGG-6.14
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_01262chr1:27471533-27472441Adrenal_Gland
SE_01262chr1:27472462-27473299Adrenal_Gland
SE_03596chr1:27471736-27472217Brain_Angular_Gyrus
SE_03596chr1:27472594-27473145Brain_Angular_Gyrus
SE_04452chr1:27471519-27472664Brain_Anterior_Caudate
SE_08182chr1:27471176-27473314Brain_Inferior_Temporal_Lobe
SE_14866chr1:27471585-27473283CD4_Memory_Primary_7pool
SE_21161chr1:27471657-27472855CD8_Memory_7pool
SE_23485chr1:27470489-27471234Colon_Crypt_1
SE_23485chr1:27471592-27472322Colon_Crypt_1
SE_23485chr1:27472448-27472910Colon_Crypt_1
SE_24258chr1:27471719-27472262Colon_Crypt_2
SE_24258chr1:27472518-27472848Colon_Crypt_2
SE_26354chr1:27471138-27473421Duodenum_Smooth_Muscle
SE_31553chr1:27470590-27473494Gastric
SE_37352chr1:27469560-27473471HSMMtube
SE_41510chr1:27471441-27473227Left_Ventricle
SE_42029chr1:27470581-27471295LNCaP
SE_42029chr1:27471647-27472190LNCaP
SE_42029chr1:27472454-27472871LNCaP
SE_42522chr1:27471452-27472992Lung
SE_49041chr1:27471448-27473071Right_Atrium
SE_50517chr1:27470565-27473097Sigmoid_Colon
SE_52500chr1:27467946-27473366Small_Intestine
SE_53642chr1:27471654-27472322Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12747180027472200
chr12747069427471273
Number: 1             
IDChromosomeStartEnd
GH01I027140chr12746674327473516
Enhancer Sequence
TAAAAATAAA TCTGCCATAG AAAGGAGATT CTGGCCCAGC CCACCCATTC CCAACACACA 60
TTAAAGCAAA GAGAAGCCAT AAGTAAATCT GTCCAGGTAC AACTATAAAT TAACAAGATT 120
GCCTTCTTGT ATGGTTTAAA GCCACTGGTC TCATTAATTC ACAGTCACAG TGCAGTTTAC 180
GGCTTGAGGA ATCTTCCCAG GAAAAGCTTA ATTCAATTAG GGCTCTCGGC AGCTCCCCAA 240
GGAAGCTCTG GTATCTTACT TTTACTTACA CAAATTGAGG GCAGACCAAA CAGATCCAGA 300
TCTTCCCAGA GAGACCCCAC CCGGCCCAGA GAAGATGCCC TTGCAGACCC TCCATTAGAG 360
CCAAGCCGAG GGAGGTGGCC AAGGCAGCAC CACTTAAACA CTGGCTGGCG CCTAAGGCAT 420
CATTCTGTGA GTGTCGCTCC CAGCGAGCTC AGTTAAACTC CTTGGCTTGG CAGTCTGGTG 480
CCAAGGAGCC TCTGCAACCT TTGCTCTCCC TCCTCTCTGA GCAGTCAAAC TGGTTTCTTG 540
TCTGCCCCAG GGCTTTGCAG GGATCCTATC TTTACACTGA AGTCAATCAC ATATTCATTC 600
ATGTATTCCT TCCCCAAATA TTTATGGAGC CTTTACTCTG TGCCAGGCAC AGATAAGAAA 660
GTGAACAGGC CAGGCGTGGT GGCTCACGCC TTTAATCTCC GCACTTTGGG AGGCCAAGGT 720
GGGTGGATCA CCTGAGGTCA GGAGTTCTAG ACCAGACTGG CCAGCATAGC AAAACCCCGT 780
CTCTACTAAA AACACAAAAA ATTAGCTGGG CGTGGTGATG TAAGCCTGTA ATCCCAGCTA 840
CTCTGGAGGC TGAGGCAGGA GAATTGCTTG AACCTGCAGC TACTCTGGAG GCTGAGGCAG 900
AATTGCTTGA ACCTGGGAGG CAGAAGTTGC AGTGAGCTGA GATCTCGCCA CTGCACTCTG 960
GCACTCCAAC CCAGGCGAAG AGCAAGACTC CATCTCAAAA AAAAAGGAAA AAGGAAAAAA 1020
AAAAAAAAAA AGAAAGTGAA CAAACAAAGT CCCTGTCCTC AAGAGGCTTA CATTCTTATG 1080
GAAATTGGTA CTAAGTATAG CCTGCTTATC TAATTCCTTT CCATCCTTCA AGACTCAGAC 1140
TAATGTTCCA CCTCCTTTGA GAGGCTTTCT CTAAACACCC CAGTCCTCAG GGACTGCTTG 1200
CTCCCTCTGT ACTTTGCCTC TGCCAGGAGT CCGCCCAGCC CTGGCAGGCT GGAAGCTCCT 1260
AAAGAGCAGG GCCTGGGTTT ACTCTTCTTT TGTTCCTTGA TGGCCATATG CTAAATGCCT 1320
GCTAGCTGAT TTCAGCTGAC CTGCCTCTTC CACCCAGGAT CTTAGCGAGC TGCTCTTGGT 1380
CCTGGCTGGC TGATGCAAAG ACACAGCCTC TTCCAGCTTC ACTTGGCATA CAGCAAATGC 1440
TATGCAAGTG TTAGCTATTT ATTGGTTTAG TGAACTTGTG GGCTCTAACA CACAGCTGTG 1500
ATATCACTCC TCCGCCTTCT GTGGCCTGGT CTCAAACAGG CTCAGCACTG TGGCAAGGCC 1560
AGTCTGGGCT TAGGGGTAAG TGCTTCCCAA GGGACAGGGA AGGGGGCCTG GGAAGGAACA 1620
GAGCTTTTCA TCCTGAATCT CAGTTAGAAC TGCTTAAGGA CATATCTTTT CAGGAAAGAA 1680
TTTGCTGGGG TAATTTGGGG GGAACTCTGG ATTCTTGGCA AGTAGTATAA AAACTCAGGG 1740
CTCAGGTCTG GCCTAATAGA CCCCAAAATC GGCTCTGTAT ATTAGATGAG CTTTAGGGGG 1800
AAGAAAATGA AGTCAGCATG ATCCCAGGGA AGGCGGGCAG CCCACTGATC CAGGCCCAAC 1860
CCAAAACTTA GTTCAGTTAA AATTAGATTA GCCCATAAGA TTAAAATACC AACATATAAT 1920
CACGGGCTGC TTTAAAGTAT CAGTTGATGT TTATCGGCAT CTAAAGAGAC AGTTTGGCCC 1980
AGTGCAGTGT GTGCAGACAA CCTTGGGGAG ACATGCCTGA CTCAGACATT TGCAGGGGGA 2040
GCGAGTGCTG CAAAATGAGG CCCACACAGG CGATGGATGA CTCAGGAATA ACCCAGGTCC 2100
TGGGTGTGCT GAGCGAGCCT TCTCTCCCTG CCTCAGGAGG AAAGGGGGCA GGTGGGAGAG 2160
GCGGTGAGGA GGAAAGGAGG CTGTGTATGG GCTGGCATTC CCAGAGACAG CCTCAGGCCC 2220
CCAGCTCTAG TTCCCCGTCA CTCCTGTATT TTTCTGCATG CTGCCACCTC TGAGAAAGGT 2280
TATTTGCTTC ACAGTGGGAC TTGGAGTGGG TCAGCTTTTT CCCCAAACCC AAGAAGTGAT 2340
CCACAGAAAG CAGCCAAGGC TCAAAATACT AAAGTCTTTA AATCTCCCCC AATTCAAAAT 2400
GATTATGGGA AAAATTGAAT TTCTAAACTG AAAAGGCCCT TGGAATCAGG GCATGAGGAT 2460
GAAAAGAACA CAGGCTCTGA AGTCAGACAA ATCTGGGCTT AAACCCCAAT GTTTTCTAGC 2520
TGTGCAAGTA CCTTTCACAA CCTCTAAACT AGATATGAAT AAGTGGCAGC TTAGCTGGAT 2580
GTGGTGACCT GTACCTGTGG TCCCAGCTAC TCAGGAGGCT GAGGTGGGGG GATTGCCTGG 2640
AGCCAGGGAG GTTGAAGCTG CAGTGAGCCG TCTTTGCGCC ACTGCACTCC 2690