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

TagContent
EnhancerAtlas ID
HS141-00928 
Organism
Homo sapiens 
Tissue/cell
NB4 
Coordinate
chr1:117045830-117047960 
Target genes
Number: 3             
NameEnsembl ID
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr1:117047152-117047163GATGAGTCACT-6.02
JUNDMA0491.1chr1:117047152-117047163GATGAGTCACT-6.32
Number of super-enhancer constituents: 14             
IDCoordinateTissue/cell
SE_09543chr1:117044641-117049783CD14
SE_12587chr1:117046105-117046497CD34_adult
SE_12587chr1:117047211-117047426CD34_adult
SE_12587chr1:117047427-117047705CD34_adult
SE_12796chr1:117045918-117046146CD34_fetal
SE_12796chr1:117046377-117046696CD34_fetal
SE_20393chr1:117044944-117048752CD56
SE_27848chr1:117046065-117048119Fetal_Intestine
SE_28774chr1:117046098-117048145Fetal_Intestine_Large
SE_39920chr1:117043259-117048495K562
SE_41250chr1:117045162-117047933Left_Ventricle
SE_50584chr1:117045995-117047955Sigmoid_Colon
SE_52493chr1:117045201-117047975Small_Intestine
SE_57245chr1:117046540-117047716VACO_400
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr1117046366117046546
chr1117047053117047428
chr1117046139117047871
Number: 1             
IDChromosomeStartEnd
GH01I116502chr1117044918117049421
Enhancer Sequence
AGCTGTGGAA GGGTCAGATG AGTCTCTGTA CAGAGAACAC ATAGCACAAT GCCTGGCCAA 60
ATTCCTGCAA ATGTCATCTG TCCTCCTTCC CTCAAACCTC TTCTCCTCCT ACTGCGGAGG 120
GGAGCACCCG AACTGGAGAA TAGAGTTAAA CTAGTTCAAA TTCTTCAAGA GTATAGTAAG 180
TGCTCAAATG TGATTTGTCC AGTTCTTTCA TATATAATAT TCACAACAAT CACATGGACC 240
AGGTATTGCT ATTCTGTTAT ACCGATGAGG AAACTGAAGG TCAGGGTTGT CTTCAGGTCA 300
TAAATAGAAC TGAGATTTGA AACTCAGTCC AGTCTACTGA ATCCAACCCC AAATACTCTT 360
GTCACAGACT GAAAGCTACA CATCAGGGGC AGATGCGGTG GCGGAGAATC CACTGGGAGA 420
GGCTTCTGCT TGGGAGTTGC TCCAGAAAGC CCTACTGGTT TATGCAATCA GACATGATCC 480
ACCCCCATGT TCTTAGGCAG CCCTGGTGCC AGGGCCTTCT CACCCTTCAT TCTAGCTGAA 540
ATGGAACCAG CATCACTGTC TCCCTATGCA AGGGGATCTC TCAACTTCCT CCTGTGGTTT 600
GTCAAGTCTT TTATATCATG ACCACTCCAA TTCATCAAAG CGTTCATGCT TATTTTGTGC 660
CTCAGTGTTT CACAATGATT TCACTCACTC CTGTTAGGTG AGTGGAGACA GCATTATTTT 720
CCTCATGTTG AGGTTGGGAG CAGGCTCAGA GCAGGCTCAG GGAGCTTCCA TCACTTGATG 780
GAGGCCCCAC AGCAGGGCCC GTGTGGGCAG CCCAGGACTC TGCACTCATG GCGCCTGCCA 840
CTGCAGAAGA CGCCCTTCAC CAGCCACTGG GTCTCAACAG TGTGGCTCCG GCAGGCCTCT 900
CAGTGGGTTT GTGTCACCCA AAGGCTGATG AAGAACAGGG GGGTGGGGTG GCAGTGAGAA 960
AGCACTTGGG AATTCAGTGA TAACAAGGTC ACCCATTCTC TCTCTGTCAG CAACTGATAG 1020
TGACAGTTGT AATAGTGACA GGCAGACCTG GATGGAAATC CTGGTTCCAC CACTGACTAG 1080
CAATGTAACC TTAACCATGT TACTACTACA CTTCCATGAG CTTCTGTTTT TCCATCTGTA 1140
TAGTGGGACT AATACTACTT ACCTACTCCT ACTGAAGGGT GAGACGCAGC AGGCAATGCG 1200
CTTAGCACAG GGCCTGGAAC ATAGTAAATG CTCAGTGGTA ATAGTGCATA GTCTTCCTTA 1260
AACTTGCAGT GACATTTATT TCACCATGAT TAGCAGCTGA GGCTGTGGGG TGACATCAGG 1320
GTGATGAGTC ACTTTGTCTG GCTGGGTCTT ACATCCGGGG CGATGTTCTG TTGCATCCAC 1380
CACCCTCCCC TGCCCCAGCT CAGGGCCCTA ACAGTCTAGC AGGGCTGGGA CTTTCTGAAA 1440
GGCTCCCCTG ACCACACCAG TTCCTCAGGA AGCCTCTCAA CCCCAGCTTC AGCTCTACTG 1500
ACATCGCCTT ACTTCCCTTT AACCCCTTTT GAGGCCCAGT TTAGAATCTG TATCTCAGCC 1560
AGAGCTCTTT CCATGCCAGC TTTGTCCACG CTGTTTACTC CTGGATAGTT CTCAGGCCCA 1620
GCCATATACC AACCCAGTGC CTGCAGTCAG GCAGACCTGG ATGGAAATCC TGGTTCTACC 1680
ACTGACTAGC AATGTAACCT TAACCATGTT ACTACTACAC TTCTATGAGC TTCTGTTTTT 1740
CCATCTATAT AGTGGGACTA ATACTACTTA CCTACTCCCA CTGAAGGGTG AGACGCAGCA 1800
GGCAATGCAC TTAGCACAGG GCCTGGAACA TAGTAAATGC TCAGTGGTAA TTCCAGCACT 1860
TTGGGAGGCT GAGGCGGTCA GATCACTTGA GTCCAGGAGT TCAAGACCAG CCTGAGCAAC 1920
ATAGTGAGAC TCTGTCATAA AAGAAAAAAA GAAATTGCTC AATGAAAGTG TGTGTGTGTG 1980
TGTGTGTTCC TCCTGAGCAT TTTACTTTTC TTTGCTATAT TTTTCCACCA TATACCAATT 2040
ACAGACCACA TGGCTCACAT CATTTCTATC TTCTCAAGCA TCCTGGTTTC TTTTCATCCT 2100
TTCTTTTGTT TTTGGCTTTC TAGCTTCTTT 2130