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

TagContent
EnhancerAtlas ID
HS105-38959 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr19:11204980-11206550 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUN(var.2)MA0489.1chr19:11205882-11205896AAGAAATGAGTCAT+7.12
JUN(var.2)MA0489.1chr19:11205887-11205901ATGAGTCATTTCCT-8.12
SREBF1MA0595.1chr19:11205756-11205766GTGGGGTGAT-6.02
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_01022chr19:11203682-11206319Adrenal_Gland
SE_01022chr19:11206333-11207663Adrenal_Gland
SE_12085chr19:11204949-11207773CD3
SE_14622chr19:11198676-11207877CD4_Memory_Primary_7pool
SE_17142chr19:11204971-11207608CD4p_CD225int_CD127p_Tmem
SE_19715chr19:11204867-11207840CD4p_CD25-_Il17p_PMAstim_Th17
SE_20994chr19:11198676-11207604CD8_Memory_7pool
SE_22774chr19:11204855-11208057CD8_primiary
SE_23239chr19:11203891-11206070Colon_Crypt_1
SE_23239chr19:11206100-11207601Colon_Crypt_1
SE_24095chr19:11204989-11205979Colon_Crypt_2
SE_24095chr19:11206049-11206285Colon_Crypt_2
SE_24095chr19:11206366-11207012Colon_Crypt_2
SE_24928chr19:11205061-11206082Colon_Crypt_3
SE_24928chr19:11206201-11206876Colon_Crypt_3
SE_26902chr19:11204916-11207828Esophagus
SE_28429chr19:11198835-11207741Fetal_Intestine
SE_29308chr19:11199027-11207595Fetal_Intestine_Large
SE_29905chr19:11204956-11208148Fetal_Muscle
SE_31737chr19:11204927-11207763Gastric
SE_34726chr19:11198191-11208606HeLa
SE_36050chr19:11204941-11207563HMEC
SE_38264chr19:11198668-11208150HUVEC
SE_40068chr19:11198411-11207591K562
SE_42817chr19:11199051-11207805Lung
SE_44493chr19:11205013-11206118NHDF-Ad
SE_44493chr19:11206328-11207705NHDF-Ad
SE_44932chr19:11205113-11207883NHLF
SE_47693chr19:11204994-11205972Pancreas
SE_47693chr19:11206022-11206280Pancreas
SE_47693chr19:11206368-11206786Pancreas
SE_49361chr19:11205119-11206191Right_Atrium
SE_49361chr19:11206197-11207709Right_Atrium
SE_50772chr19:11198863-11207767Sigmoid_Colon
SE_52540chr19:11198883-11208401Small_Intestine
SE_54059chr19:11198844-11207806Spleen
SE_57847chr19:11205007-11205595VACO_503
SE_64571chr19:11204940-11207695NHEK
SE_65732chr19:11198652-11207882Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191120569611206011
Enhancer Sequence
CGGCTAATTT TGTATTTTTC GTAGAGATGG GGTTTCTCCA CATTGGTTCA GGCTGTTCTC 60
GAACTCCCAA CCTCAGGTGA TCCACCCGCC TCAGCCTCCC AAAGTGCTGG GATTATAGGC 120
GTGAGCCCCC GAACCCGGCC ACTCCCAGCT AAGTTTAAAT TTTTTGTTTG TTTGTTCGTT 180
TGTTTTTATT TTTTGAGACA GAGTCTCCCG CCCAGGCTGG AGCGCAGATC ACTGCATCCT 240
TGACCTCCCA GGCTTAAGCC ATCCTCCCCA CTCAGCCTCC CAAGTAGCTG GGATTACAGG 300
TGTGTGCCAC TATGCTTGGC TAAGTTGTGT ATTTTTTGTA GAGATGGGGT TCAAGGGATT 360
CTCGCTTTGT TGCCTCGGTT GGTCTCAAAC TCCTGGGCTC AAGCAGTCCT CCCTCCTCAG 420
CCTCCCAAGG TGCTGGGGAA ATCCACTTTT GAAACATTGT CTGGAGAGTT GCCCAGGTGG 480
TAGATCACAG AAATAGGTCA TCGTGGGGTC CTTCCCATGG GTGCAGTCTT GAGCCACCTG 540
TGGCCAGCAA ATATTTGGAG AATAATAGTC AGGGGAGAGC TTGAGGTCCA GGGAAAGGTT 600
TTGTTTTTCT TCAGGGAAAG GTTTTTATTG TTCTTTATCC CTCCTTAAAG GACCTTCAGG 660
TGTTACTGAC ATTCCCGGTC TACCCAGTGG CACATTTAGT TTGTAAGCTG GGCCCTCGTA 720
CAGAGGTAGG GAGGTGAGAG CATTGGATTA GTGGTCACCA AAGCTGCGGT CACCTAGTGG 780
GGTGATCAGA GGCTCCTCCC TTAAGATCTT GATTGCCAAC GCCTCTGGCC CAACTTTCCT 840
TTTTATTTAT CGCAAGCCTC CTGGAATCTC AATTGCTTTT TGCCCACCCG GTGTGTCAGC 900
ACAAGAAATG AGTCATTTCC TCCTTTAAGC ACAGTTGAAA TTGAGCTGTG AGTCAGTGAG 960
GTGTGTACGA TATTGTCAAA GCGGGGTGTG TACAGTATTG ACAGATCTGT AGTTGGGCAA 1020
GAGAATTATC AGAGTTTGTG ACCACAGCAG ATTCCAAAGC TCGACTCATT TTCTTCTCTC 1080
TTCCTTCCCT TTTTTCTTTT CTTTTTTTTT TTTTTTTTGA CAGAGTCTCG CTCTGTTGCC 1140
CAGGCTGGAG TGCAGTGGCA CAATCTGGGC TCACTGCAGC CCCTGCCTCC TGGGTTCAAA 1200
TGATTCTCAT GTTTCAGCCT CCCGAGTAGC TGCAATTACA GGCATTCGGG TTCAAGTGAT 1260
TCTCCTGCCT CAGCCACCTG AGCAGCTGGG ATTACAGGCG CCCGCCACCA CGCCCGGCTA 1320
ATTTTTGTAT TTTTAGTAGA GACGGGGTTT CACCATGTTG GCCAGGCTGG TCTCGAACTC 1380
CTGAACTCAG GTGATCCGCC CACTTCGGCC TCCCAAAGTG CTGAGATTAC AGACGTGAGT 1440
CACCGCGCCC AGCCTGTTCT GTTCTTTAAT TCTCAAAACA CCCTCTAGGA AGTAGAGACT 1500
GCCATTCTCC CCCATTTTAC AGATCAGGAA ACTGAGTCCC AGAAGGATTT AGTCAGTTAC 1560
CCAAGTTGTT 1570