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

TagContent
EnhancerAtlas ID
HS098-17424 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr14:55574040-55575810 
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: 33             
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_46880chr14:55575591-55575827Ovary
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
GATTACAGAC GTCCATCAAC ACGCCCAGCT AATTTTTGTA TTTTTAGTAG AGATAGGGTT 60
TCACCATGTT GGCCAGGCTG GTCTTGAACT GCCTACCTCA GGTGATCCAC CCACCTTGGC 120
CTCCCAAAGT GCTGGGATTA CAGGCGTAAG CCACCTGCGC CTGGCCGGTA TTTTTAAATT 180
AGAGTTCTTC TAAGATTTAT CTGAAAAAGT TACACTACTA AAAAATTTGC AACCCACACC 240
CAAGGACATA ATTTGTCTGG GCATAGAGAC TTGATGGCAC TTCAAGTAGC TGGATGAGCT 300
TCTCTTAACA TGCGATTTCT CTCAGGTTTA CATTCTTCTT GACTGCCCTT GTTCCTTTCC 360
TATTCTATTT GAAGCAAAAT GGTTAACGTT CTTCCACTTT CACCAGGACA GCCCTATTTG 420
CCCCTTCCTT GTCCTTGTTA GCCTGGTTTT ATAAAGCCTC TTTTGCAGGG GTCGGAACAG 480
TTAATAGCAT TGGGGATTGT CGCTTGTTCC CTGTAGATGA AAAGTATTTT TCTATTGTTT 540
AAAAAAAAAT CGAGGTCATT CTCCAAAGTA ATTTCCTGAA ATAAAGCGTG GGAGGAAGTC 600
ATGGGCATGA GGATGAGTCA TCAGGCAGCA GCACGAGGCT GCAGGCGTGA GCTGGGGAGC 660
CCTGGCTCAG TCCTCCGCAG GCTTGGATCC CTGAGCGGAG CAGGCCACTG GGGCCTTCTG 720
CCGTGAGAAG AGACCTACTG AGAGGCGGGG AGTGGGGGTG GGAGTGGTTG CTTCTGACCT 780
GTAGGACAGT GGTCAGCGTG GGCGGGTGGA GGCACAGGAG AAGGCCGACA GGCCCTGGGT 840
CCTAGGGCCA CTCAGCTGCT GGAAAATGAA GTTCAGAGTT GTTTGGACTG TCTGAAGTAG 900
GATAGAACCA GCCTTAGCCC TAGTTAGGTA ACACATGGCA GAGGCACCTG AGCAAAGACG 960
TGAGCTGGAC CATGGGCTTC CTGGCAGGAC TTCCACGGAG GAGGGCGAGG GGAGAGGAGC 1020
AAGGGAGCAG AAGGCAGCTT GCCGTCCACG AAGCCTCCTG AGGCCCCAGA TGAGTCACCA 1080
GACAACAGCC TGTCTACTTA AAGCAACTGC TGGGCAACTG CTGAGTAGAA CAGTCCCTAA 1140
CCACATGAAC ACTGGGGAGG AGGTTCTGAA AGACGCTGCT GGGTGCAAGG TCCCTAACTA 1200
GGGTAATCCA ATTTCACTCC AGGCTAACAT GAGAAATTAT GACTCCAGCA GCCAATCCTG 1260
TGGGCCGTGA GAGAGTGGGA GAGGGATTTT CCAGATATAA GTCCCACTAG AGCTTCTTTT 1320
TTTTTTTTTT TTTTGATACG GAGTCTCACT CTGTTATCCA CGCTGGAGTG CAGTGGCACC 1380
ATCTCGGCTC ACTGCAAGCT CCGCCTCCCG GGTTCAAGCG ATTCTGTTGC CCCAGCCTCC 1440
TGAGCAGATG GGACTACAGA TGTGCACCAC CATGCCCAGC TAATTTTTGT ATTTTTAGTA 1500
GAGACAGGGT TTCACTATGT CGGCCAGGCT GGTCTCGAAC TCCTGACCTC ATGATTCTCC 1560
TGCCTTGGCC TCCTAAAGTG TTGGGATCAC TGGCATAAGC CACAGCTTCC GGCTGAGTCC 1620
CACTAGAGCT TCTAAGAAGA AATTAGGGAA GCAGGATTAT GAGAGGCCTG GTCCCACTCA 1680
CAGTGTGCGA CATCACTGAT GACTATGCTT GGTTACCTGC CTTGTTATTT GCTACCTTTG 1740
TTATTGTCTA TTTCTTGGTA ATTAGTAGTA 1770