EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-24268 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr14:55573580-55576440 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr14:55575108-55575119GATGAGTCACC-6.32
IRF1MA0050.2chr14:55576267-55576288GTCCAGTTTCAATTTCTTTAT+6.01
JUNDMA0491.1chr14:55575108-55575119GATGAGTCACC-6.62
ZNF263MA0528.1chr14:55575036-55575057GGAGGAGGGCGAGGGGAGAGG+7.74
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_00244chr14:55563236-55576350Adipose_Nuclei
SE_00820chr14:55574748-55575102Adipose_Tissue
SE_02600chr14:55573844-55576160Astrocytes
SE_09388chr14:55568067-55576360CD14
SE_23110chr14:55574129-55575416Colon_Crypt_1
SE_23790chr14:55574594-55575269Colon_Crypt_2
SE_24786chr14:55574109-55575428Colon_Crypt_3
SE_26013chr14:55573672-55575878Duodenum_Smooth_Muscle
SE_26711chr14:55573567-55575917Esophagus
SE_27630chr14:55573899-55576071Fetal_Intestine
SE_28543chr14:55573873-55576230Fetal_Intestine_Large
SE_31668chr14:55574018-55575868Gastric
SE_33558chr14:55573897-55579764H2171
SE_34039chr14:55574107-55575498HCC1954
SE_34802chr14:55573592-55576155HeLa
SE_36310chr14:55573891-55575863HMEC
SE_37768chr14:55573433-55575974HSMMtube
SE_41170chr14:55573962-55575665Left_Ventricle
SE_42472chr14:55573658-55575611Lung
SE_44570chr14:55573874-55576148NHDF-Ad
SE_45117chr14:55573558-55575933NHLF
SE_46036chr14:55573692-55576091Osteoblasts
SE_46880chr14:55574151-55574573Ovary
SE_46880chr14:55574627-55575401Ovary
SE_49010chr14:55574074-55575920Right_Atrium
SE_50181chr14:55574075-55575919Sigmoid_Colon
SE_52430chr14:55573656-55575984Small_Intestine
SE_56717chr14:55573869-55576081u87
SE_57551chr14:55574279-55575356VACO_503
SE_64542chr14:55574036-55575714NHEK
SE_66903chr14:55573897-55579764H2171
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr145557426455575347
chr145557446555575376
Number: 1             
IDChromosomeStartEnd
GH14I055097chr145556377555576469
Enhancer Sequence
AATTATTTCT TTTGTGTTTT TATCTTTTAT TGTTTTTTGA GACAGAGTCT CACTCTGTTG 60
CCCAGGCTGG AGTACAGTGG CTTGATCTCG GCTCACTACA ACCTCCACCT CCTGGTTCAA 120
GTGATTGTCC TGTCTCACCC TCCCCAGTAA CTGGGATTAC AGGCGCCCAC CACCACACCC 180
AGGTAATTCT TGTGTTTTTG TAGAGGTGGG GTCTCGCCAT GTTGTCCAGG CCGGTCTGGA 240
ACTCCTGGCC TCAAGCGATC TGCCCGCCTC AGCCTCCCAA AGTGCTGGGG TTACAGGCGT 300
GAGCCACTGC GCCCGGCCTC CTTGGTATTT TTATGTCTAT TTTTTTAGAT GGAGTCTCGC 360
TCTGTCCCCC AGGCTGGAGT GCAGTGGCGC GATCAGCTCA CTGCAACCTC CACCTCGCGG 420
GTTCAAGCAA TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATTACAGAC GTCCATCAAC 480
ACGCCCAGCT AATTTTTGTA TTTTTAGTAG AGATAGGGTT TCACCATGTT GGCCAGGCTG 540
GTCTTGAACT GCCTACCTCA GGTGATCCAC CCACCTTGGC CTCCCAAAGT GCTGGGATTA 600
CAGGCGTAAG CCACCTGCGC CTGGCCGGTA TTTTTAAATT AGAGTTCTTC TAAGATTTAT 660
CTGAAAAAGT TACACTACTA AAAAATTTGC AACCCACACC CAAGGACATA ATTTGTCTGG 720
GCATAGAGAC TTGATGGCAC TTCAAGTAGC TGGATGAGCT TCTCTTAACA TGCGATTTCT 780
CTCAGGTTTA CATTCTTCTT GACTGCCCTT GTTCCTTTCC TATTCTATTT GAAGCAAAAT 840
GGTTAACGTT CTTCCACTTT CACCAGGACA GCCCTATTTG CCCCTTCCTT GTCCTTGTTA 900
GCCTGGTTTT ATAAAGCCTC TTTTGCAGGG GTCGGAACAG TTAATAGCAT TGGGGATTGT 960
CGCTTGTTCC CTGTAGATGA AAAGTATTTT TCTATTGTTT AAAAAAAAAT CGAGGTCATT 1020
CTCCAAAGTA ATTTCCTGAA ATAAAGCGTG GGAGGAAGTC ATGGGCATGA GGATGAGTCA 1080
TCAGGCAGCA GCACGAGGCT GCAGGCGTGA GCTGGGGAGC CCTGGCTCAG TCCTCCGCAG 1140
GCTTGGATCC CTGAGCGGAG CAGGCCACTG GGGCCTTCTG CCGTGAGAAG AGACCTACTG 1200
AGAGGCGGGG AGTGGGGGTG GGAGTGGTTG CTTCTGACCT GTAGGACAGT GGTCAGCGTG 1260
GGCGGGTGGA GGCACAGGAG AAGGCCGACA GGCCCTGGGT CCTAGGGCCA CTCAGCTGCT 1320
GGAAAATGAA GTTCAGAGTT GTTTGGACTG TCTGAAGTAG GATAGAACCA GCCTTAGCCC 1380
TAGTTAGGTA ACACATGGCA GAGGCACCTG AGCAAAGACG TGAGCTGGAC CATGGGCTTC 1440
CTGGCAGGAC TTCCACGGAG GAGGGCGAGG GGAGAGGAGC AAGGGAGCAG AAGGCAGCTT 1500
GCCGTCCACG AAGCCTCCTG AGGCCCCAGA TGAGTCACCA GACAACAGCC TGTCTACTTA 1560
AAGCAACTGC TGGGCAACTG CTGAGTAGAA CAGTCCCTAA CCACATGAAC ACTGGGGAGG 1620
AGGTTCTGAA AGACGCTGCT GGGTGCAAGG TCCCTAACTA GGGTAATCCA ATTTCACTCC 1680
AGGCTAACAT GAGAAATTAT GACTCCAGCA GCCAATCCTG TGGGCCGTGA GAGAGTGGGA 1740
GAGGGATTTT CCAGATATAA GTCCCACTAG AGCTTCTTTT TTTTTTTTTT TTTTGATACG 1800
GAGTCTCACT CTGTTATCCA CGCTGGAGTG CAGTGGCACC ATCTCGGCTC ACTGCAAGCT 1860
CCGCCTCCCG GGTTCAAGCG ATTCTGTTGC CCCAGCCTCC TGAGCAGATG GGACTACAGA 1920
TGTGCACCAC CATGCCCAGC TAATTTTTGT ATTTTTAGTA GAGACAGGGT TTCACTATGT 1980
CGGCCAGGCT GGTCTCGAAC TCCTGACCTC ATGATTCTCC TGCCTTGGCC TCCTAAAGTG 2040
TTGGGATCAC TGGCATAAGC CACAGCTTCC GGCTGAGTCC CACTAGAGCT TCTAAGAAGA 2100
AATTAGGGAA GCAGGATTAT GAGAGGCCTG GTCCCACTCA CAGTGTGCGA CATCACTGAT 2160
GACTATGCTT GGTTACCTGC CTTGTTATTT GCTACCTTTG TTATTGTCTA TTTCTTGGTA 2220
ATTAGTAGTA CACTATAGTG ATTAGGAGTG ATCAAGAAGA TGCCTGGCTT CATATTCCAA 2280
CTTTGTCGTT TACTAACTGT GAACTTGGCC GAGTTTTTTT TTTTTTGCTT GTTTGTTTTG 2340
TTTTGAGACA GGATCTCTCT CTGTCACCCA GGCTGGAGTG CAGTGGCGTG ATCTCAGCTC 2400
ACTGCAACCT CCACCTCCTG GAATCAAGGG ATCCTCCCAC CTTAGCCTCC CAAGTAGCTG 2460
AGATACACGT GTGCACCATC ACACCTGGCT AATTTTTGTA TTTTTTGTAG AGATGGTGTT 2520
TCACCATGTT GCCCAGGCTG GTCTTGAAGC CCTGGGCTCA AGCCATCACC CACCTTGGCC 2580
TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACCTCCTGA CCTCAGGTGA TCCACCTGCC 2640
TCAGCCTCCC AAAGTGTTGG GATTACAGGC ATGAGCCACT GTGGCCAGTC CAGTTTCAAT 2700
TTCTTTATTT GTAAATTTGT AATAATGACA GGACTAGCTC TTAGCCAGAA GCAGCAGCTC 2760
TTGCCTGTAA TCCCAGCACT TTGGGAAGTT GAGGTGGATG GATCACTTGA GGCCAAGAGT 2820
TTGAGATCAG CCTCAGCAAC ATGGCAAGAC CCCCATCTCT 2860