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

TagContent
EnhancerAtlas ID
HS111-01444 
Organism
Homo sapiens 
Tissue/cell
KB 
Coordinate
chr14:55574090-55575750 
Target genes
Number: 8             
NameEnsembl ID
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr14:55575108-55575119GATGAGTCACC-6.32
JUNDMA0491.1chr14:55575108-55575119GATGAGTCACC-6.62
ZNF263MA0528.1chr14:55575036-55575057GGAGGAGGGCGAGGGGAGAGG+7.74
Number of super-enhancer constituents: 32             
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_23790chr14:55574297-55574562Colon_Crypt_2
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
AGATAGGGTT TCACCATGTT GGCCAGGCTG GTCTTGAACT GCCTACCTCA GGTGATCCAC 60
CCACCTTGGC CTCCCAAAGT GCTGGGATTA CAGGCGTAAG CCACCTGCGC CTGGCCGGTA 120
TTTTTAAATT AGAGTTCTTC TAAGATTTAT CTGAAAAAGT TACACTACTA AAAAATTTGC 180
AACCCACACC CAAGGACATA ATTTGTCTGG GCATAGAGAC TTGATGGCAC TTCAAGTAGC 240
TGGATGAGCT TCTCTTAACA TGCGATTTCT CTCAGGTTTA CATTCTTCTT GACTGCCCTT 300
GTTCCTTTCC TATTCTATTT GAAGCAAAAT GGTTAACGTT CTTCCACTTT CACCAGGACA 360
GCCCTATTTG CCCCTTCCTT GTCCTTGTTA GCCTGGTTTT ATAAAGCCTC TTTTGCAGGG 420
GTCGGAACAG TTAATAGCAT TGGGGATTGT CGCTTGTTCC CTGTAGATGA AAAGTATTTT 480
TCTATTGTTT AAAAAAAAAT CGAGGTCATT CTCCAAAGTA ATTTCCTGAA ATAAAGCGTG 540
GGAGGAAGTC ATGGGCATGA GGATGAGTCA TCAGGCAGCA GCACGAGGCT GCAGGCGTGA 600
GCTGGGGAGC CCTGGCTCAG TCCTCCGCAG GCTTGGATCC CTGAGCGGAG CAGGCCACTG 660
GGGCCTTCTG CCGTGAGAAG AGACCTACTG AGAGGCGGGG AGTGGGGGTG GGAGTGGTTG 720
CTTCTGACCT GTAGGACAGT GGTCAGCGTG GGCGGGTGGA GGCACAGGAG AAGGCCGACA 780
GGCCCTGGGT CCTAGGGCCA CTCAGCTGCT GGAAAATGAA GTTCAGAGTT GTTTGGACTG 840
TCTGAAGTAG GATAGAACCA GCCTTAGCCC TAGTTAGGTA ACACATGGCA GAGGCACCTG 900
AGCAAAGACG TGAGCTGGAC CATGGGCTTC CTGGCAGGAC TTCCACGGAG GAGGGCGAGG 960
GGAGAGGAGC AAGGGAGCAG AAGGCAGCTT GCCGTCCACG AAGCCTCCTG AGGCCCCAGA 1020
TGAGTCACCA GACAACAGCC TGTCTACTTA AAGCAACTGC TGGGCAACTG CTGAGTAGAA 1080
CAGTCCCTAA CCACATGAAC ACTGGGGAGG AGGTTCTGAA AGACGCTGCT GGGTGCAAGG 1140
TCCCTAACTA GGGTAATCCA ATTTCACTCC AGGCTAACAT GAGAAATTAT GACTCCAGCA 1200
GCCAATCCTG TGGGCCGTGA GAGAGTGGGA GAGGGATTTT CCAGATATAA GTCCCACTAG 1260
AGCTTCTTTT TTTTTTTTTT TTTTGATACG GAGTCTCACT CTGTTATCCA CGCTGGAGTG 1320
CAGTGGCACC ATCTCGGCTC ACTGCAAGCT CCGCCTCCCG GGTTCAAGCG ATTCTGTTGC 1380
CCCAGCCTCC TGAGCAGATG GGACTACAGA TGTGCACCAC CATGCCCAGC TAATTTTTGT 1440
ATTTTTAGTA GAGACAGGGT TTCACTATGT CGGCCAGGCT GGTCTCGAAC TCCTGACCTC 1500
ATGATTCTCC TGCCTTGGCC TCCTAAAGTG TTGGGATCAC TGGCATAAGC CACAGCTTCC 1560
GGCTGAGTCC CACTAGAGCT TCTAAGAAGA AATTAGGGAA GCAGGATTAT GAGAGGCCTG 1620
GTCCCACTCA CAGTGTGCGA CATCACTGAT GACTATGCTT 1660